Pharmaceutical Development Scientist
Associate principal scientist job in Columbus, OH
The Pharmaceutical Development Scientist is a hands-on technical role responsible for the formulation, development, optimization, and technology transfer of sterile and non-sterile drug products across STAQ Pharma's 503B Outsourcing Facilities. Reporting directly to the Chief Pharmaceutical Officer, this position supports product development initiatives from concept through scale-up and commercialization, driving innovation, process improvement, and lifecycle management of compounded drug products.
The scientist collaborates closely with Manufacturing Sciences & Technology (MS&T), Quality, and Production teams to translate laboratory-scale formulations into scalable, validated CGMP manufacturing processes. Responsibilities include conducting pre-formulation and compatibility studies, preparing R&D and pilot-scale batches, and analyzing analytical and stability data to identify optimal formulations that maximize quality, performance, and product expiration dating.
This role requires strong analytical chemistry expertise-including the ability to interpret UPLC chromatograms, assess impurity profiles, and apply ICH and FDA 503B guidance-to guide formulation strategy, product development, and technology transfer activities.
Key Responsibilities:
Develop, optimize, and scale formulations for sterile and non-sterile dosage forms in compliance with CGMP, FDA 503B, and ICH guidelines.
Conduct pre-formulation studies, excipient compatibility testing, and stability evaluations to inform formulation design and shelf-life optimization.
Design and execute experiments to assess formulation feasibility, process robustness, and long-term product stability.
Prepare and manufacture laboratory-scale, R&D, and pilot-scale batches for testing and process development.
Lead and support technology transfer activities for new and existing products, ensuring seamless transition from R&D to manufacturing and between STAQ Pharma sites.
Conduct literature reviews and data analysis to identify innovative formulation approaches and support development strategy.
Analyze data from HPLC, GC, dissolution, and stability studies to assess potency, purity, and impurity profiles.
Collaborate with MS&T, Quality, and Production teams to ensure manufacturing processes are robust, validated, and scalable.
Develop and execute stability protocols, trend data, and prepare detailed technical summaries and reports.
Write and maintain technical documentation, including batch records, development protocols, SOPs, and technical reports in accordance with CGMP standards.
Support investigations of out-of-specification (OOS) or out-of-trend (OOT) results and contribute to CAPA development and implementation.
Participate in audits, inspections, and internal quality reviews to ensure regulatory and operational compliance.
Qualifications:
Bachelor's, Master's, or Ph.D. in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related discipline.
Minimum of 3-5 years of hands-on experience in CGMP pharmaceutical formulation or product development (503B, CDMO, or sterile pharma manufacturing preferred).
Demonstrated experience in formulation design, stability testing, and technology transfer.
Proficiency in analytical chemistry techniques, including UPLC, GC, and dissolution testing; ability to interpret chromatograms and impurity profiles.
Strong working knowledge of ICH Q8-Q10, FDA 503B guidance, and applicable USP chapters.
Experience in scale-up and process optimization for aseptic and non-sterile drug products.
Excellent technical writing, communication, and organizational skills.
Ability to work independently, prioritize multiple projects, and collaborate effectively across cross-functional teams and sites.
Associate Scientist
Associate principal scientist job in Columbus, OH
Title: Associate Scientist
Duration: 12 Months
Shift: Monday- Friday, 8am -5pm
Main Responsibilities:
• Sensory Scientist with 1-2 years of experience to support sensory testing and product evaluation.
• This role involves preparing and managing sensory panels, handling and presenting samples, and maintaining lab organization.
• The candidate will assist in designing and executing sensory studies using basic scientific principles and experimental design.
• Responsibilities also include collecting and organizing data, supporting analysis, and ensuring tests are conducted accurately and consistently.
Skills:
• Worked in Lab environments.
• Background in food science, psychology, Sensory science or related field- Biology or chemistry (scientific principles) is preferred.
• Strong attention to details
• Strong communication both verbal and written.
• Familiarity with sensory methods and lab environments
• Experience with Compusense software is a plus
Education:
• Bachelors degree in any field related to Food science, Psychology, Sensory science, biology, Chemistry.
Additional: Looking for 1-2 years experience
Clinical Variant Scientist
Remote associate principal scientist job
Title: Clinical Variant Scientist (Part-Time, Remote)
Company: Machaon Diagnostics
Employment Type: Part-Time (10 hrs/week)
About Us
Machaon Diagnostics is a specialized clinical reference laboratory and CRO focused on hematology, immunology and rare disease diagnostics. We support physicians, hospitals, and pharma/biotech partners by delivering fast, high-quality molecular and functional testing. Our genetics program includes next-generation sequencing assays, somatic and germline variant interpretation, and the development of innovative assays in complement biology, immune dysregulation, and related pathways.
About the Role
Machaon Diagnostics is seeking a part-time, remote Clinical Variant Scientist to support our growing genetics program focused on rare disease, immunology, hematology, and complement biology. You'll play a key role in variant interpretation, report drafting, and assay-development support.
This role offers flexible hours, remote work, and meaningful impact in clinical diagnostics.
What You'll Do
Interpret germline and/or somatic variants using ACMG/AMP guidelines
Review NGS data, QC metrics, and annotation outputs
Curate variants using ClinVar, gnom AD, HGMD, and related databases
Draft clear, concise clinical reports
Maintain and update internal variant knowledge bases
Support new assay development and validation
Ensure compliance with CLIA/CAP standards and SOPs
What We're Looking For
Required:
MSc or PhD in Genetics, Genomics, Molecular Biology, or related field
1-3+ years experience in clinical variant interpretation
Preferred:
Experience with rare disease, immune dysregulation, or complement biology
Prior work in a CLIA/CAP-accredited lab
What We Offer
Part-time remote role (approx. 10 hrs/week)
Flexible schedule
Opportunity to contribute to innovative rare-disease diagnostics
Supportive and collaborative team environment
How to Apply
Submit your CV and a brief note about your variant-interpretation experience to:
james.kain at machaondiagnostics.com
Subject:
Clinical Variant Scientist - Part-Time
Associate Principal Data Scientist (Remote)
Remote associate principal scientist job
Your Role Within Our Kingdom We are seeking an Associate Principal Data Scientist-a highly experienced and technically deep individual contributor who leads through influence, owns high-impact initiatives, and drives scientific excellence across experimentation and modeling.
(This position is open to remote work.)
Responsibilities:
* Lead the design and execution of large-scale data science initiatives, shaping the roadmap for experimentation and modeling across teams.
* Apply advanced statistical, optimization, and machine learning techniques (e.g., time-series, regression/classification, recommendation engines, reinforcement learning, and gen AI) to drive system understanding and develop data-powered solutions across the organization.
* Own design and evaluation of experimentation for optimization systems.
* Provide technical direction, mentor senior data scientists, and set high standards for scientific rigor, communication, and reproducibility.
* Partner cross-functionally with Product, Engineering, and Game Studios to frame ambiguous problems, scope solutions, and influence strategy.
* Champion innovation by evaluating new methodologies and tools, and by raising the bar for scalable, interpretable, and actionable data science.
Skills to Create Thrills
Minimum Qualifications:
* Master's degree or PhD in a quantitative field (e.g., Statistics, Mathematics, Computer Science, Economics, Engineering, Operations Research).
* 14+ years of industry experience (or equivalent post-graduate experience) in data science, experimentation, statistical modeling, and machine learning, including work with large-scale systems.
* Proficient in Python and SQL; familiarity with big data tools (e.g., Spark, Hive) and cloud computing platforms (e.g., GCP, AWS).
* Strong systems thinking-able to zoom out and define strategy while also diving deep into code and analysis.
* Excellent communication and collaboration skills, with demonstrated experience partnering across Product, Engineering and Business teams.
* Demonstrated experience mentoring, influencing, and elevating the technical bar across a data science organization.
* Relevant experience with one or more advertising solutions (i.e. Real-Time Bidding, Ad Exchange, etc.)
Bonus Points
* Prior work with mobile gaming studios or player behavior modeling.
* Experience in developing or maintaining experimentation platforms.
* Familiarity with modern data orchestration and versioning (e.g., Airflow, dbt, MLflow).
We love hearing from anyone who is enthusiastic about changing the games industry. Not sure you meet all qualifications? Let us decide! Research shows that women, veterans, and members of other under-represented groups tend to not apply to jobs when they think they may not meet every qualification, when, in fact, they often do! We are committed to creating a diverse and inclusive environment and strongly encourage you to apply.
We are committed to working with and providing reasonable assistance to individuals with physical and mental disabilities. If you are a disabled individual requiring an accommodation to apply for an open position, please email your request to accommodationrequests@activisionblizzard.com. General employment questions cannot be accepted or processed here. Thank you for your interest.
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, gender identity, age, marital status, veteran status, or disability status, among other characteristics.
Rewards
We provide a suite of benefits that promote physical, emotional and financial well-being for 'Every World' - we've got our employees covered! Subject to eligibility requirements, the Company offers comprehensive benefits including:
* Medical, dental, vision, health savings account or health reimbursement account, healthcare spending accounts, dependent care spending accounts, life and AD&D insurance, disability insurance;
* 401(k) with Company match, tuition reimbursement, charitable donation matching;
* Paid holidays and vacation, paid sick time, floating holidays, compassion and bereavement leaves, parental leave;
* Mental health & wellbeing programs, fitness programs, free and discounted games, and a variety of other voluntary benefit programs like supplemental life & disability, legal service, ID protection, rental insurance, and others;
* If the Company requires that you move geographic locations for the job, then you may also be eligible for relocation assistance.
Eligibility to participate in these benefits may vary for part time and temporary full-time employees and interns with the Company. You can learn more by visiting ***************************************
In the U.S., the standard base pay range for this role is $143,060.00 - $264,846.00 Annual. These values reflect the expected base pay range of new hires across all U.S. locations. Ultimately, your specific range and offer will be based on several factors, including relevant experience, performance, and work location. Your Talent Professional can share this role's range details for your local geography during the hiring process. In addition to a competitive base pay, employees in this role may be eligible for incentive compensation. Incentive compensation is not guaranteed. While we strive to provide competitive offers to successful candidates, new hire compensation is negotiable.
Auto-ApplyApplied Scientist
Remote associate principal scientist job
About the company:
The mining industry has steadily become worse at finding new ore deposits, requiring >10X more capital to make discoveries compared to 30 years ago. The easy-to-find, near-surface deposits have largely been found, and the industry has chronically under-invested in new exploration technology, relying on the manual techniques of yesteryear - even as demand accelerates for copper, lithium, and other metals to build electric vehicles, renewable energy, and data centers.
KoBold builds AI models for mineral exploration and deploys those models-alongside our novel sensors-to guide decisions on KoBold-owned-and-operated exploration programs. In the six years since founding, KoBold has become by far both the largest independent mineral exploration company and the largest exploration technology developer. Our data scientists and software engineers, who come from leading technology companies, jointly lead exploration programs with our renowned exploration geologists.
KoBold has proven its first discovery with materially less capital than the industry average and found one of the best copper deposits ever discovered: the copper is far more concentrated than the global average of copper mines, and this asset alone is expected to generate meaningful revenue for decades. KoBold has a portfolio of more than 60 other projects, each of which has the potential for another high-quality discovery.
KoBold is privately held; investors include institutional asset managers T. Rowe Rice and Canada Pension Plan Investments; technology venture capitalists Andreessen Horowitz, Breakthrough Energy Ventures, BOND Capital, and Standard Investments; and natural resources companies Equinor, BHP, and Mitsubishi.
About The Role:
In this role, you will develop state of the art instruments to collect data to guide our exploration programs. You will simulate, characterize, and calibrate sensor performance and design new data acquisition systems. Working with vendors and partners, you will build hardware and work with our operations staff to deploy it in the field.
With this sensor data and other data sources at KoBold, you will build models and apply a wide range of scientific computing, statistical, and physics-based methods to find places where there is evidence of ore-forming processes at work and to predict the locations of ore-grade mineralization in 2D and 3D. You will help build a worldwide dataset that underlies our exploration program, with careful attention to identifying and quantifying uncertainty in the data and in our predictions. You will be creating models and developing software to accelerate discovery of critical battery metals.
You will join an outstanding team of data scientists and engineers and will work closely with KoBold's world-renowned geoscientists to incorporate our best understanding of the chemical and physical processes that create ore deposits. Working with your geoscience colleagues, you will identify new opportunities and technologies for geophysical data collection, create 2D and 3D geologic predictions, identify exploration targets, design field programs to collect data, and use that data to reduce the uncertainty in our predictions and guide the next phase of field work.
Ultimately, your role is to help KoBold make valuable discoveries by building and deploying next generation hardware and using data tools to solve scientific problems. As one of the early members of this team, you will help build these tools from the ground up.
Responsibilities of this position include:
Technical execution
Design, develop, and deploy new mineral exploration data collection instruments and methods.
Help develop KoBold's proprietary software exploration tools.
Find and curate a wide variety of geospectral, geophysical, geochemical, geologic, and geographic data and integrate it into KoBold's proprietary data system.
Build models to make statistically valid predictions about the locations of compositional anomalies within the Earth's crust.
Create effective visualizations for evaluating model performance and enabling rapid interaction with the underlying data and key features.
Develop and apply a range of data processing, statistical, and physics-based techniques to geoscientific data - from computer vision to geophysical inversions - and use the results to guide our targeting efforts and inform our acquisition and exploration decisions.
Present to and collaborate with our external partners and stakeholders.
Push the state of the art in analysis capabilities by implementing statistically rigorous spatially aware clustering, anomaly detection, and other analysis methods
Collaborate with data scientists, geoscientists and engineers to invent and deploy algorithms that combine large and complex data sets for mineral exploration and discoveries
Qualifications
Demonstrated ability to quickly absorb and synthesize complex information, with a track record of high intellectual rigor in a professional setting.
Exceptional curiosity and eagerness to learn, with a proactive approach to exploring new concepts and technologies.
A successful track record of developing complex equipment with cross-disciplinary teams and vendors.
Technical skills, including extensive experience with:
Physical measurement and data analysis systems that use phenomena such as optics, electromagnetism, radiation, and gravity.
Applying scientific knowledge to identify and prototype emerging technologies
Systems integration and data acquisition.
Python's data science packages and general software engineering practices.
Collaborative software development (git), and familiarity with software engineering best practices like unit test / integration test suites, and CICD pipelines.
SQL, as well as familiarity with non-relational databases.
Cloud computing resources.
Building a wide variety of predictive models, applying them to different problems, and evaluating and interpreting the results.
Data analysis, physics analysis, and applied statistics on a broad range of types of data including data from physical systems.
Capacity to dive deep on novel challenging problems in applying ML to mineral exploration, including understanding a complex domain of geology and mineral exploration practices as well as working with limited, disparate and noisy data sources
Experience deploying sensors in the field
Work practices and motivation:
Ability to take ownership and responsibility of large projects.
Intellectual curiosity and eagerness to learn about all aspects of mineral exploration, particularly in the geology domain. Open to working directly with geologists in the field. Enjoys constantly learning such that you are driving insights and innovations.
Ability to explain technical problems to and collaborate on solutions with domain experts who aren't software developers. A strong communicator who enjoys working with colleagues across the company.
Excitement about joining a fast-growing early-stage company, comfort with a dynamic work environment, and eagerness to take on a range of responsibilities.
Keen not just to build cool technology, but to figure out what technical product to build to best achieve the business objectives of the company.
Ability to independently prioritize multiple tasks effectively.
It is also helpful but not required to have experience with:
Remote sensing
Creating machine learning models on geospatial data
Image processing or computer vision
Project and team management
KoBold Metals is an equal opportunity workplace and an affirmative action employer. We are committed to equal employment opportunity for people of any race, color, ancestry, religion, sex, gender identity, sexual orientation, marital status, national origin, age, citizenship, disability, or veteran status.
This position is Full-time Exempt
Salary is one part of KoBold's total compensation. The US salary range for this role is between $125,000 and $235,000, and will depend on your skills, qualifications, experience, and location. In addition to salary, we offer equity compensation. We also offer benefits including medical, dental, and vision insurance, a 401k retirement plan, short & long term disability and life insurance. We also offer paid sick time and parental leave."
Location: Remote, Candidates can be located anywhere in the United States or Canada. All candidates must be legally authorized to work in the United States or Canada. 10-20% travel required.
Auto-ApplyAI Omics Scientist III (Remote - US)
Remote associate principal scientist job
This position is posted by Jobgether on behalf of a partner company. We are currently looking for an AI Omics Scientist III in the United States.
This role offers an exciting opportunity to lead the design and deployment of advanced AI and machine learning models in the field of genomics and multi-omics research. You will play a pivotal part in developing predictive and generative models that accelerate discoveries in diagnostics, therapeutic development, and precision medicine. Working remotely with cross-functional teams of scientists, engineers, and clinicians, you will design scalable, production-ready AI pipelines, ensuring reproducibility, interpretability, and clinical relevance. This position combines high-level technical expertise with scientific creativity and leadership.
Accountabilities:
Lead the design and implementation of machine learning models for multi-omics data analysis and clinical AI applications.
Integrate genomic, transcriptomic, proteomic, and clinical datasets to create scalable and interpretable AI solutions.
Develop and optimize deep learning architectures, including CNNs, RNNs, transformers, and LLMs, for predictive and generative modeling.
Deploy production-ready models using MLOps frameworks, containerized environments, and cloud-native platforms.
Mentor junior scientists, guide project direction, and ensure scientific rigor in all AI-driven research activities.
Collaborate with data engineering and clinical teams to translate computational models into actionable insights.
Publish research findings, contribute to open-source projects, and maintain high standards of transparency and reproducibility.
Requirements
PhD in Computational Biology, Bioinformatics, Artificial Intelligence, or a related field with 4+ years of experience, or MS with 6+ years of experience.
Strong expertise in omics technologies (RNA-seq, WGS, single-cell, proteomics) and biomedical informatics.
Deep understanding of machine learning, statistical modeling, and biological data interpretation.
Proficiency in Python and modern ML frameworks such as PyTorch, TensorFlow, JAX, or HuggingFace.
Experience with GPU-based training, distributed learning systems, and cloud computing platforms (AWS, GCP).
Skilled in MLOps tools (MLflow, DVC), Docker/Kubernetes, and data pipeline orchestration (Nextflow, Snakemake).
Experience with foundational AI models (BERT, BioBERT, GPT, AlphaFold, or domain-adapted LLMs).
Familiarity with HIPAA-compliant and regulated environments.
Excellent communication skills and proven ability to work across scientific and engineering disciplines.
Track record of peer-reviewed publications, conference presentations, or open-source contributions.
Benefits
Competitive annual salary ranging from $140,000 to $175,000, plus a Short-Term Incentive Plan (10% of annual earnings).
Full remote work flexibility within the United States (PST preferred).
Comprehensive medical, dental, and vision insurance.
401(k) plan with company match and flexible spending accounts (FSA).
Generous paid time off (PTO) and paid sick leave.
Continuous learning and professional development support.
Inclusive, collaborative culture that values scientific innovation and open exchange of ideas.
Equal opportunity employer supporting second-chance employment and fair hiring practices.
Jobgether is a Talent Matching Platform that partners with companies worldwide to efficiently connect top talent with the right opportunities through AI-driven job matching.
When you apply, your profile goes through our AI-powered screening process designed to identify top talent efficiently and fairly.
🔍 Our AI evaluates your CV and LinkedIn profile thoroughly, analyzing your skills, experience, and achievements.
📊 It compares your profile to the job's core requirements and past success factors to determine your match score.
🎯 Based on this analysis, we automatically shortlist the 3 candidates with the highest match to the role.
🧠 When necessary, our human team may perform an additional manual review to ensure no strong profile is missed.
The process is transparent, skills-based, and free of bias - focusing solely on your fit for the role. Once the shortlist is completed, we share it directly with the company that owns the job opening. The final decision and next steps (such as interviews or additional assessments) are then made by their internal hiring team.
Thank you for your interest!
#LI-CL1
Auto-ApplyPharmacovigilance Scientist
Remote associate principal scientist job
About Us:
Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit ***************
As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture.
Job Title: Pharmacovigilance Scientist
Location: Remote
Role Overview:
The Pharmacovigilance Scientist plays a critical role in the collection, evaluation, and management of drug safety data throughout clinical development. This role supports the monitoring and assessment of adverse events, safety signal detection, and risk management activities to safeguard patient safety and ensure regulatory compliance. The Pharmacovigilance Scientist collaborates with cross-functional teams to maintain the integrity of safety data and contributes to the preparation of safety-related documentation, presentations and aggregate reports. They work closely with the Senior Medical Director, Pharmacovigilance and Safety, to execute pharmacovigilance strategies.
Key Responsibilities:
Safety Data Collection and Review:
Collects, reviews, and analyzes adverse event reports from clinical trials to identify potential safety signals
Supports quality control review of individual case safety reports (ICSRs)
Assists in ongoing safety monitoring activities, including data reconciliation and quality checks to ensure accuracy of safety data.
Supports safety data management activities, including case processing, follow-up, and coding of adverse events
Risk Assessment and Signal Detection:
Assesses clinical safety data to identify, evaluate, and document adverse events and emerging safety concerns.
Contributes to risk-benefit analyses and supports the development of risk mitigation strategies
Pharmacovigilance Documentation:
Supports the preparation and review of pharmacovigilance documents such as Development Safety Update Reports (DSURs), development Risk Management Plans (dRMPs), and relevant sections of clinical trial protocols, IBs and regulatory submissions
Proficient with safety surveillance systems and tools (e.g., Argus, MedDRA, Veeva Vault)
Scientific Expertise:
Maintains current knowledge of relevant therapeutic areas, pharmacology, and drug safety regulations
Conducts literature reviews and safety signal assessments to inform safety evaluations
Cross-Functional Collaboration:
Works closely with clinical operations, regulatory affairs, medical affairs, data management, bioinformatics and project management teams to ensure comprehensive safety oversight
Supports compliance with global pharmacovigilance regulations and company safety policies
Supports the communication and oversight of pharmacovigilance and contract research organization vendors
Supports the project management of safety activities such as aggregate reports, safety team meetings, signal evaluations, etc.
Qualifications:
Advanced degree in life sciences (e.g., PharmD, PhD) or related field
Minimum of 3 years of experience within the pharmaceutical industry, ideally including drug safety experience
Knowledge of good pharmacovigilance practices, drug safety regulations, and clinical trial processes
Understanding of pharmacovigilance regulatory practices including CIOMS, EMA, ICH and FDA guidelines
Experience with adverse event data review, safety signal detection, and safety database management (e.g. Argus, MedDRA, Veeva Vault)
Strong analytical, communication and presentation skills
Strong organizational and project management skills
Ability to collaborate effectively across multidisciplinary teams in a fast-paced environment
Compensation:
An appropriate financial package will be developed for the successful candidate to include a competitive base salary and equity, with a performance-related bonus opportunity.
The anticipated salary range for candidates, Scientist I is $125,000-140,000 and Scientist II is $140,000-155,000 . The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Oruka is a multi-state employer and this salary range may not reflect positions that work in other states.
If located within one of our offices in Waltham, MA or Menlo Park, CA, you will be required to go into office 3 days a week.
We're looking forward to hearing how you can contribute to our team and mission. Join us in shaping the future of our company and making a real impact every day.
Salary Range for the Role$125,000-$155,000 USD
What We Offer:
A chance to be part of a vibrant startup culture where your work can directly impact bringing new medicines to patients.
Competitive salary and benefits package.
A supportive and inclusive team environment where everyone is encouraged to bring their authentic selves to work.
Opportunities for professional growth and development.
Auto-ApplyScientist II
Remote associate principal scientist job
Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA, visit our website ********************************** or follow us on LinkedIn.
Job Overview
We are currently seeking a dynamic, highly motivated, and experienced individual for the position of Scientist II. This position will be part of the Translational Research and Medicine-Oncology team, with a primary focus on advancing translational research to support oncology programs in clinical trial stages. This individual will be responsible for designing, oversighting, and interpretating translational studies to understand mechanism of action, resistance pathways, and potential new indications. The candidate may also be involved in biomarker analysis to support these translational objectives.
Job Duties and Responsibilities
Develop hypotheses by integrating insights from scientific literature, preclinical and clinical data
Design experiments to support identification of mechanism of action, resistance mechanisms, and potential indications
Manage translational research and biomarker studies conducted with CROs and academic investigators to ensure high-quality, timely delivery of data
Maintain organized, detailed logs of studies and data to ensure accuracy, reproducibility, and compliance with regulatory standards
Present data and insights in internal meetings and cross-functional program team discussions
Key Core Competencies
Scientific curiosity with ability to generate and test hypotheses that inform drug development
Excellent problem-solving and critical-thinking skills to interpret complex data
Strong organizational skills and attention to detail in managing studies, data, and documentation
Strong project management and vendor oversight skills
Adaptability and resilience in a fast-paced, evolving research environment
Education and Experience
PhD degree in a related field of science (Biology, Biochemistry, Molecular & Cellular biology, Cancer Biology, Immunology)
1-3 years of postdoctoral or industry research experience
Familiarity with oncology research preferred
Experience with common biomarker platforms (e.g. NGS, flow cytometry, IHC) preferred
The base salary range for this role is $102,000 to $127,000. Base salary is part of our total rewards package which also includes the opportunity for merit-based salary increases, short incentive plan participation, eligibility for our 401(k) plan, medical, dental, vision, life and disability insurances and leaves provided in line with your work state. Our robust time-off policy includes flexible paid time off, 11 paid holidays plus additional time off for a shut-down period during the last week of December, 80 hours of paid sick time upon hire and each year thereafter. Total compensation, including base salary to be offered, will depend on elements unique to each candidate, including candidate experience, skills, education and other factors permitted by law.
Disclaimer: The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed.
Confidential Data: All information (written, verbal, electronic, etc.) that an employee encounters is considered confidential.
Compliance: Achieve and maintain Compliance with all applicable regulatory, legal and operational rules and procedures, by ensuring that all plans and activities for and on behalf of Sumitomo Pharma America (SMPA) and affiliates are carried out with the "best" industry practices and the highest ethical standards.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Mental/Physical Requirements: Fast paced environment handling multiple demands. Must be able to exercise appropriate judgment as necessary. Requires a high level of initiative and independence. Excellent written and oral communication skills required. Requires ability to use a personal computer for extended periods of time.
Sumitomo Pharma America (SMPA) is an Equal Employment Opportunity (EEO) employer
Qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
Auto-ApplyScientist I - Ecologist/Biologist
Remote associate principal scientist job
Sundance Consultants, a part of True Environmental and its partner firms, have united their strengths to establish the nation's premier environmental and engineering services consulting firm. This powerhouse organization offers an extensive range of services aimed at revolutionizing the built environment and preserving the natural one. Its diverse expertise encompasses environmental remediation, urban planning, engineering iconic coastal and marine structures, developing sustainable energy sources, and pioneering resource extraction methods. Explore further at Sundance-inc.com and True-Environmental.com to discover the full scope of our capabilities.
Responsibilities will include providing support for natural resources assessments and management activities with a heavy emphasis on field surveys, field assessments and biological monitoring. Willingness to assist in project planning, field studies, data entry, report writing to document field study results, permitting, and administrative office support. The successful candidate will assist in a wide range of natural resources projects which will include field studies to support flora and fauna surveys, habitat assessments and management, threatened and endangered species surveys, ecological monitoring and wetland and aquatic resources characterizations and assessments. What you'll do
Field Technician duties include:
Use Global Positioning System (GPS) units to document locations and remote monitoring plots and transects.
Perform various resource management and monitoring activities;
Collect and record technical field data; and,
Other duties as assigned.
Administrative Support duties include:
Provide administrative support or assistance to personnel in the office.
Create and prepare documents using Microsoft Word and Excel and Adobe Acrobat (PDF);
Operate office equipment such as printers, copy machines, and fax machines; and,
Other duties as assigned.
Minimum Qualifications
Bachelor's degree in Biology, Ecology, Environmental Studies, Natural Resources or related science.
Experience performing data collection in the field, documenting results of data collection into formal reports, and experience using GPS in support of field studies.
Experience with wildlife and plant identification and an understanding of ecological resources management.
3+ years of computer skills, preferably in Microsoft Office Professional (Word, Excel, Outlook, and Power Point). Ability to learn new programs.
Must be able to manage multiple projects concurrently and prioritize work effectively.
Ability to work with minimal supervision and with general directions.
Ability to satisfactorily pass pre-employment and post-employment drug and alcohol tests.
Must possess a valid driver's license.
Ability to satisfactorily pass post-employment physical.
Ability to work outdoors in variable weather conditions.
Ability to lift up to 30lbs. on occasion.
Preferred Qualifications
Completed at least five (5) terrestrial vegetation surveys identifying native and nonnative plant species found in limestone and secondary forests in the Marianas.
Documented ability to work in remote setting in a karst environment without direct on-site supervision or assistance.
DoD certification or Guam certification in Pest Control.
Knowledge of endangered species in Guam.
Experience using ArcView/ArcMap Geographic Information System
Excellent verbal and written communication skills.
Detail oriented and organized.
Must work well under pressure.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
Auto-ApplyModern AI Scientist
Remote associate principal scientist job
Thank you for your interest in joining Solventum. Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. At Solventum, people are at the heart of every innovation we pursue. Guided by empathy, insight, and clinical intelligence, we collaborate with the best minds in healthcare to address our customers' toughest challenges. While we continue updating the Solventum Careers Page and applicant materials, some documents may still reflect legacy branding. Please note that all listed roles are Solventum positions, and our Privacy Policy: *************************************************************************************** applies to any personal information you submit. As it was with 3M, at Solventum all qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Job Description:
AI Scientist - Modern AI Applications
3M Health Care is now Solventum
At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers' toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue.
We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you.
The Impact You'll Make in this Role
As a Principal AI Scientist with deep expertise in Agentic AI, Generative AI, and Natural Language Understanding (NLU), you will lead high-impact technical innovation in HIS applications. In this role, you will be a hands-on research and development leader - driving technical breakthroughs, designing novel AI architectures, and directly influencing the integration of advanced AI into mission-critical healthcare products. You will collaborate closely with other scientists, engineers, and domain experts to create solutions that are explainable, reliable, and transformative for healthcare operations.
Key Responsibilities
Research & Innovation
Design, prototype, and evaluate novel AI models for autonomous, agent-based systems in healthcare workflows.
Advance state-of-the-art NLU for clinical, operational, and administrative healthcare text.
Explore and implement new capabilities in reasoning, decision-making, and multi-modal understanding.
Healthcare-Focused AI Development
Adapt and fine-tune large language models to handle healthcare-specific language, regulatory requirements, and ethical considerations.
Create AI pipelines that can process structured and unstructured healthcare data (FHIR, HL7, clinical notes, claims data).
Contribute to domain-specific model architectures that improve clinical decision-making, revenue cycle management, and patient engagement.
Technical Leadership
Serve as the primary technical authority on Agentic and Generative AI within project teams.
Mentor junior AI scientists and engineers through code reviews, research guidance, and technical workshops.
Drive internal knowledge-sharing on emerging AI trends, frameworks, and best practices.
Operational & Compliance Excellence
Implement rigorous model evaluation frameworks for accuracy, robustness, and fairness.
Ensure compliance with healthcare privacy and data security regulations (HIPAA, HITRUST).
Partner with engineering to move research prototypes into production environments.
Required Qualifications
Master's in Computer Science, AI, Machine Learning, or related field AND 5+ years of experience in AI/ML, with a strong portfolio of deployed models.
Or
PhD in Computer Science, AI, Machine Learning, or related field AND 3+ years of experience in AI/ML, with a strong portfolio of deployed models.
Experience in Python, R, and modern ML libraries.
Experience with GenAI, LLMs, and transformer architectures.
Experience with AI development tools and frameworks (PyTorch, TensorFlow, Hugging Face, LangChain, RAG systems).
Preferred Skills
Multi-modal AI research experience (text, image, structured data).
Knowledge graph integration and symbolic reasoning expertise.
Proven ability to take AI research from concept to production.
Hands-on experience with autonomous AI agents and reasoning systems.
Strong track record applying AI to healthcare or life sciences use cases.
Familiarity with cloud platforms (AWS) and MLOps practices.
Work location:
US Remote
Travel: May include up to 10% domestic
Relocation Assistance: Is not authorized
Must be legally authorized to work in the country of employment without sponsorship for employment visa status (e.g., H1B status).
Supporting Your Well-being
Solventum offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, Solventum regularly benchmarks with other companies that are comparable in size and scope.
Onboarding Requirement: To improve the onboarding experience, you will have an opportunity to meet with your manager and other new employees as part of the Solventum new employee orientation. As a result, new employees hired for this position will be required to travel to a designated company location for on-site onboarding during their initial days of employment. Travel arrangements and related expenses will be coordinated and paid for by the company in accordance with its travel policy. Applies to new hires with a start date of October 1st 2025 or later.Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties.
Solventum is committed to maintaining the highest standards of integrity and professionalism in our recruitment process. Applicants must remain alert to fraudulent job postings and recruitment schemes that falsely claim to represent Solventum and seek to exploit job seekers.
Please note that all email communications from Solventum regarding job opportunities with the company will be from an email with a domain *****************. Be wary of unsolicited emails or messages regarding Solventum job opportunities from emails with other email domains.
Please note, Solventum does not expect candidates in this position to perform work in the unincorporated areas of Los Angeles County.Solventum is an equal opportunity employer. Solventum will not discriminate against any applicant for employment on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status.
Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly.
Solventum Global Terms of Use and Privacy Statement
Carefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at Solventum are conditioned on your acceptance and compliance with these terms.
Please access the linked document by clicking here, select the country where you are applying for employment, and review. Before submitting your application you will be asked to confirm your agreement with the
terms.
Auto-ApplyScientist, Mass Spectrometry and Critical Reagents
Remote associate principal scientist job
The Role:
The Scientist will be responsible to support the protein quantification and proteomics analysis using Mass spectrometry for PK and PD studies, ensuring the timely and efficient management of critical reagents used in the development, validation, and execution of bioanalytical and molecular assays to support clinical assays at Moderna. The successful candidate will work closely with cross-functional teams for protein analysis, qualify critical reagents, as well as establish and maintain robust systems for their monitoring, tracking, and storage. This is in person laboratory based position located in Norwood, MA.
Here's What You'll Do:
Support LC-MS based protein quantification/proteomics assay development, validation and sample analysis under regulatory compliance.
A solid background in modern analytical techniques used in the analysis of mRNA-based therapeutic products is essential.
Maintain a robust system for the monitoring, tracking, and storage of critical reagents to ensure their availability and quality. Support reagent characterization to generate CoA documentation.
Knowledge of peptide/proteins, aptamer-antibody based conjugation systems for DNA, RNA, and Protein/antibodies.
Maintain a database of Reference standards/reagents, including their specifications, source, usage, and expiration dates.
Conduct regular audits of critical reagent inventory and work with cross-functional teams to manage the procurement and disposition of the reagents.
Vendor management to ensure the availability and quality of critical reagents.
Develop and implement policies, procedures, and training programs to ensure compliance with regulatory requirements and industry best practices.
Collaborate with cross-functional teams to develop reagent-specific risk assessments and mitigation strategies.
Monitor industry trends and advancements in critical reagent management and implement the best practices to improve efficiency and effectiveness.
Here's What You'll Need (Basic Qualifications)
Ph.D. in a scientific field, such as chemistry, biochemistry, or biology with 3+ years of experience in Bioanalytical Sciences/regulated bioanalysis. M.S. with at least 7 years of bioanalytical experience will also be considered.
Strong knowledge of critical reagents management as well as current industry best practices and regulatory requirements.
Deep understanding of Proteomics/Protein mass spectrometry for PK and biomarker analysis
Demonstrated ability to work collaboratively with cross-functional teams to achieve shared goals.
Excellent organizational, analytical, and problem-solving skills.
Proven ability to manage multiple projects simultaneously and prioritize tasks in a fast-paced environment.
Here's What You'll Bring to the Table (Preferred Qualifications):
Experience with the Biophysical Characterization of Biologics (LCMS, SDS-PAGE, cIEF, SPR, BLI, SEC-HPLC, SEC-MALS, UV-VIS)
Experience working in a GLP environment (ELN/LIMS/automation)
Experience with HRMS and software for protein analysis/characterization
At Moderna, we believe that when you feel your best, you can do your best work. That's why our US benefits and global well-being resources are designed to support you-at work, at home, and everywhere in between.
Best-in-class healthcare coverage, plus a suite of voluntary benefit programs to support your unique needs
A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
Lifestyle Spending Accounts to personalize your well-being journey
Family planning and adoption benefits
Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
Savings and investment opportunities
Location-specific perks and extras
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.
If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Our Working Model
As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.
Moderna is a smoke-free, alcohol-free, and drug-free work environment.
Equal Opportunities
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!
Moderna is an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Accommodations
We're focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations team at leavesandaccommodations@modernatx.com.
Export Control Notice
This position may involve access to technology or data that is subject to U.S. export control laws, including the Export Administration Regulations (EAR). As such, employment is contingent upon the applicant's ability to access export-controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements, only individuals who qualify as U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible for this position. For this role Moderna is unable to sponsor non-U.S. persons to apply for an export control license.
#LI-NB1
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Auto-ApplyFishery Restoration Scientist
Remote associate principal scientist job
Seeking a Fishery Restoration Scientist to support NOAA Fisheries in executing analytical, technical, and field-related tasks across multiple habitat conservation and environmental review programs. This position will work closely with the NOAA Project Lead (PL) to evaluate project impacts, conduct habitat analyses, support regulatory reviews, and develop high-quality technical deliverables. The work will be performed in a fully remote capacity, with only a limited possibility of occasional travel within the east coast regions of Florida, South Carolina, North Carolina, or Georgia.
The task includes the following:
* Review study objectives developed by the Southeast Region and project partners, identify optimal field study locations, manage partner-provided datasets, develop associated metadata, and recommend practicable refinements to future field efforts. Deliver short technical reports and data files and incorporate all NOAA PL comments into final documentation.
* Analyze project-specific data to evaluate compliance with hydropower facility license conditions, with particular attention to fish passage and flow prescriptions. Deliver concise written reports for each facility and revise final documentation in response to NOAA PL comments.
* Assess effects to Essential Fish Habitat (EFH) and evaluate proposed mitigative measures for offshore wind energy projects using data provided. Prepare short written reports and develop briefing materials suitable for NOAA senior leadership summarizing project objectives, expected impacts, benefits, and anticipated schedules. Address all NOAA PL comments in final deliverables.
* Review dredging operation data and coral condition information for the Port Everglades and Port Miami project areas. Evaluate potential effects to coral habitat, recommend mitigation measures to offset expected impacts, and deliver a written report containing habitat characterizations and supporting GIS files with appropriate metadata and Google Earth files. Address all NOAA PL comments in final documentation.
* Conduct EFH, Fish and Wildlife Coordination Act (FWCA), and Fish and Wildlife Planning Assistance (FPA) analyses for proposed construction and restoration projects. Maintain a current understanding of diadromous, estuarine, and reef fish habitats, key environmental pressures, and conservation partnerships across Southeast U.S. watersheds. Use GIS to prepare maps and manage spatial data for analysis, and produce written reports and briefing materials with complete responses to NOAA PL comments.
* Submit electronic monthly progress reports that clearly correlate cost, level of effort, activity descriptions, and accomplishments for the reporting period.
Requirements
* Knowledge of fish and habitat ecology, environmental conservation principles, and habitat impact assessment methodologies.
* Experience conducting data analysis, preparing technical summaries, and managing fisheries or environmental datasets.
* Experience using GIS software for spatial analysis, map production, and metadata development.
* Familiarity with EFH assessments, environmental review processes, and habitat-based conservation strategies within marine or estuarine systems.
* Ability to write clear, concise technical reports and prepare briefing materials for senior decision-makers.
* Strong proficiency with common software including word processing, spreadsheets, statistical tools, data management applications, and the entire Google suite.
* Ability to collaborate with partners, manage multiple ongoing tasks, and respond to technical comments with accuracy and completeness.
* Must be a US Citizen or Permanent Resident who has lived in the United States at least 3 of the last 5 years and must be able to pass a background investigation to obtain a security badge to access applicable government systems.
Work Location
This position is fully remote in support of NOAA Fisheries.
Education
Bachelor's degree in Biology, Marine Science, Ecology, Environmental Science, or a related discipline, plus three years of experience in fish biology, marine biology, oceanography, or a closely related field.
Salary
The salary range for this role is $46,000 - 221,000/year. This range is a good faith estimate based on similar roles across the organization. ERT considers several factors when extending an offer of employment, including the location, scope, and associated responsibilities of the specific position, as well as a candidate's work experience, education/training, and key skills.
Benefits
All full-time employees are eligible to participate in our flexible benefits package, which includes:
* Medical, Rx, Dental, and Vision Insurance
* 401(k) retirement plan with company-matching
* 11 Paid Federal Government Holidays
* Paid Time Off (PTO)
* Basic Life & Supplemental Life
* Health Savings Account, Flexible Spending and Dependent Care Flexible Spending Accounts
* Short-Term & Long-Term Disability
* Employee assistance program (EAP)
* Tuition Reimbursement, Personal Development & Learning Opportunities
* Skills Development & Certifications
* Professional Membership Reimbursement
* Employee Referral Program
* Competitive compensation plan
* Discretionary variable incentive bonuses based on factors such as individual performance, business unit performance, and/or the company's performance
* Publication and Conference Presentation Awards with bonuses
ERT is a VEVRAA Federal Contractor and Equal Opportunity employer - All qualified applicants will be considered for employment without regard to race, color, religion, sex, national origin, disability, or protected Veteran status.
#LI-Remote
Machine Learning Scientist (Remote Allowed)
Remote associate principal scientist job
NOMA AI Mission:
NOMA is developing a novel AI platform for healthcare that leverages deep tech and machine learning to analyze multimodal medical data and help clinical teams proactively identify risks of medical complications. Our first product focus is on maternal hemorrhage and excessive bleeding of mothers that can happen during labor and delivery and continues to rank as a leading cause of maternal mortality and morbidity in the U.S.
The Opportunity:
NOMA AI Inc. is looking for candidates for a machine learning research engineer position to participate in developing cutting-edge machine learning and data analytic solutions in healthcare. The successful applicant will participate in the development, research, evaluation, and deployment of machine learning methodologies for real-time clinical decision systems, patient monitoring, and alerting solutions. Our team includes individuals with strong machine learning, software engineering, and healthcare backgrounds. In addition, we wish to reach out to talented individuals who are passionate about revolutionizing healthcare and who are interested in:
Working on problems that are at the forefront of both industry and scientific research in ML for healthcare
Researching, developing, and deploying real-time machine learning-based AI tools in healthcare.
Achieving long-term and ambitious product development goals while identifying intermediate milestones
Being independent problem solvers while operating in a collaborative environment
Requirements
Qualifications:
Ph.D. degree in Computer science, Machine Learning, AI, or another equivalent field
Relevant publications
Ability to rapidly iterate and evaluate machine learning methodologies to solve novel problems
Experience working with popular machine learning frameworks, including NumPy, Pandas, Scikit-learn, PyTorch, TensorFlow
Experience working with high-frequency signal and waveform data
Experience with time-series data, high-frequency data, prediction modeling, and imbalanced data
Expert Knowledge of Python.
Have experience in working and collaborating with others on team projects
Ability to deliver with limited guidance, working on problems that are not structured
5+ years of programming experience
Preferred Qualification:
Experience with medical data, electronic health records, biosensor data, etc.
Experience with real-time environments and model deployment
Experience with major cloud environments and other distributed systems
Interest and experience in software engineering (data pipelines)
BenefitsHealth insurance, 401(k), vision, dental, PTO, maternity/paternity leave,
Staff Applied Machine Learning Scientist
Remote associate principal scientist job
Medium's mission is to deepen understanding of the world and spread ideas that matter. We are building the best place for reading and writing on the internet-a place where today's smartest writers, thinkers, experts, and storytellers can share big, interesting ideas; a place where ideas are judged on the value they provide to readers, not the fleeting attention they can attract for advertisers.
Role Overview
One of Medium's core operating principles is “humans first,” but sometimes to do that we need a little help from machine learning-which is why Medium is looking for an experienced Staff Applied ML Scientist to join our team. First and foremost, you'll own Medium's recommendation systems, which serves millions of readers every day by parsing through an ocean of posts and curating perfect literary pearls for each of them. Under the hood, it's a sophisticated and modern ML pipeline, fueled by a two-tower model and separate deep retrieval and ranking stages.
Beyond recommendations, you'll also develop ML models to protect our readers from the burgeoning world of AI slop and spam, explore and evangelize new applications for machine learning across Medium's business, and leverage machine learning to ensure that Medium always puts humans first.
Key Responsibilities
You'll help us apply machine learning thoughtfully across Medium - starting with recommendations, but extending far beyond them. You'll look for places where ML can make the reading and writing experience more personal, relevant, and human.
Experiment with ideas like smarter
post discovery
that helps writers find their natural audience.
Explore opportunities for personalization, quality detection, topic modeling, or even AI-assisted editorial curation - all grounded in improving understanding, not chasing engagement for its own sake.
Work closely with design, product, and engineering partners to translate ambiguous user needs into well-framed ML problems.
Drive the research. Lead with curiosity and precision. You'll design and interpret experiments, bring statistical rigor to our experimentation, and keep a critical eye on things like bias and spurious correlation in our thinking.
Bring organizational leverage. Work across teams to ensure that ML improvements are well-integrated into the product, not off to the side. You'll regularly influence decision-making through cross-functional collaboration, helping product and engineering leaders spot where ML can create leverage and where it shouldn't.
Own and continuously improve our recommendation systems. Evolve our two-tower retrieval and ranking stack, refine our feature set, and push on model quality, latency, and interpretability.
Find new and innovative ways to use ML techniques to better serve our community of readers and writers. This might mean smarter spam and slop detection, writer quality modeling, or intelligent routing of human moderation. The goal: keep Medium a place where humans thrive, not bots.
Positively contribute to the broader culture and data ecosystem at Medium. Mentor others, document your work with clarity, and help raise the bar for how we think about, design, and deploy ML systems. Share learnings generously and make the people and systems around you better.
Attend Medium's twice-yearly, in-person offsites (hosted in locations around the U.S.).
Skills, Knowledge and Expertise
You've been designing and building software for at least 7 years, with at least 3 years focused on architecting and shipping consumer-facing ML models.
You have experience integrating ML into end-user products (recommendation, ranking, personalization, moderation). You have a proven track record of developing and deploying ML models that deliver measurable business and user impact, not just theoretical gains.
You embody the “applied” in applied ML: You enjoy the research, but love seeing models ship, move metrics, and make people's experiences better.
You're fluent in Python and ML libraries such as TensorFlow, HuggingFace Transformers, and scikit-learn. You're comfortable taking models from notebook to production. It's a huge added bonus if you have experience with Apache Spark for distributed or large-scale training.
You're an excellent collaborator, able to translate between data, product, design, and engineering worlds, helping non-ML partners see what's possible (and what's not). You're excited to be “the voice of ML” in business and product conversations.
You're skilled at identifying and evangelizing high-leverage ML opportunities across the organization, from recommendation systems to new personalization or quality signals.
You have hands-on experience with modern model architectures and techniques e.g., feature interaction modeling, advanced negative sampling and bias correction techniques, and efficient large-scale candidate retrieval.
(Bonus) You're curious about content discovery, publishing, or online communities, and have a soft spot for writing, ideas, and helping great work get found.
Nice to Haves
Experience with modern recommender systems.
Experience utilizing modern AI tooling to accelerate development efforts.
A passion for online writing, publishing, or long-form content.
Familiarity with Medium, as a reader, writer, or both!
Benefits
In addition to the new skills you'll pick up, here's what else you'll enjoy by working at Medium:
Working with a fully distributed team: We're fully remote and have teammates across the U.S. & France.
Healthcare benefits covered at 100% for employees and 70% for dependents.
Generous parental leave policy.
Mental health support through Talkspace.
Financial wellness support through Northstar.
Stipends for co-working, professional development, wifi, and a one-time home office bonus.
Unlimited PTO and standard company holidays.
A discounted Medium membership!
At Medium, inclusion, diversity, and equity are core to how we work and what we build. We believe a more inclusive team creates a better product-one that's intuitive, thoughtful, and serves a wide range of users. We strive to foster a supportive, fun, and challenging environment where people from all backgrounds can thrive.
We welcome applicants from all walks of life and strongly encourage those from historically underrepresented groups to apply. Our hiring process is built to ensure fairness and equal opportunity for everyone. Even if your experience doesn't match every requirement, we'd still love to hear from you-your perspective and passion matter more than checking every box.
Learn more about our mission, operating principles, and culture:
Yes to a diverse community
Be part of a better internet
Medium Rules
Operating Principles
Read about our story here.
Please note: We've been made aware that our job postings may appear on third-party sites that are not affiliated with our company. To ensure your application is received and reviewed, please apply directly through our official Greenhouse careers page. We do not collect applications through external job boards or services that request your personal information outside of Greenhouse.
Additionally we request that all applications and supplemental questions be filled out directly by applicants themselves without the use of AI assistance.
Salary Range$250,000-$300,000 USDGDPR Notice
We will process your personal data as part of our recruitment process, in accordance with the General Data Protection Regulation (GDPR). For details on how we use your data, including the legal bases for processing, how long we retain it, and your rights under GDPR, please refer to our Privacy Notice.
We may retain your information for future job opportunities based on our legitimate interest in building a talent pool. You can object to this at any time by contacting us at *********************.
CCPA Notice
If you are a California resident, you have rights under the California Consumer Privacy Act (CCPA), as amended by the California Privacy Rights Act (CPRA). These include the right to know what personal information we collect about you, the right to request deletion or correction of your data, and the right to opt out of certain uses.
During the hiring process, we may collect personal information such as your name, contact details, resume/CV, employment history, education background, and any information gathered through interviews or assessments. We may share this information with service providers who support our recruitment process, in compliance with CCPA/CPRA. This information is used solely for recruitment and hiring purposes.
We do not sell or share your personal information as defined under CCPA/CPRA. Candidate data is retained for up to 48 months for our legitimate business purposes and in accordance with applicable laws.
To exercise your rights or request more information, please contact us at *********************. This notice can also be found on our Privacy Notice.
Auto-ApplyAssociate Scientist I
Associate principal scientist job in Columbus, OH
**Main Responsibilities:** - Sensory Scientist with 1-2 years of experience to support sensory testing and product evaluation. - This role involves preparing and managing sensory panels, handling and presenting samples, and maintaining lab organization.
- The candidate will assist in designing and executing sensory studies using basic scientific principles and experimental design.
- Responsibilities also include collecting and organizing data, supporting analysis, and ensuring tests are conducted accurately and consistently.
**Skills:**
- Worked in Lab environments.
- Background in food science, psychology, Sensory science or related field- Biology or chemistry (scientific principles) is preferred.
- Strong attention to details
- Strong communication both verbal and written.
- Familiarity with sensory methods and lab environments
- Experience with Compusense software is a plus
**Education** :
- Bachelors degree in any field related to Food science, Psychology, Sensory science, biology, Chemistry.
**Additional** : Looking for 1-2 years experience
**About US Tech Solutions:**
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit *********************** (*********************************** .
US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
**Recruiter Details:**
Name: Rahul Singh
Email: *****************************
Easy ApplyWFP Machine Learning Scientist
Associate principal scientist job in Columbus, OH
JobID: 210689616 JobSchedule: Full time JobShift: Day : The Workforce Planning (WFP) organization is a part of Consumer and Community (CCB) Operations division. The WFP Data Science organization is tasked with delivering quantitatively driven solutions to support the core WFP functions (demand forecasting, capacity planning, resource scheduling, and business analysis & support). The WFP organization supports Chase's call centers, back office, and ~5,200 retail branches.
As a Data Scientist Lead - WFP Machine Learning Scientist, within JPMorganChase, you will engage in projects by the Artificial Intelligence(AI)/Machine Learning(ML) team that can be complex, data intensive, and of a high level of difficulty, each having significant impact on the business. You will typically encounter these problems which will be of an unstructured nature, whereby the employee will be expected to quickly assess and comprehend the situation then develop a practical problem solving strategy. You will be expected to analyze the topic in question, develop solution proposals and review their results and next steps with management for prioritization, timing, and delivery. The AI/ML team is tasked with building next-gen data science solutions that move us closer to real-time inference and decision making.
Job Responsibilities
* Design and development of Machine Learning, Artificial Intelligence and Statistical models.
* Participate in the full model development lifecycle, from framing the problem to prepare documentation and passing independent model review (MRGR).
* Lead AI/ML projects along with mentor and coach junior team members.
* Collaborate with stakeholders to understand the business requirements and clearly define the objectives of any solution.
* Identify and select the correct method to solve the problem while staying up to data on the latest AI/ML research
* Ensure the robustness of any data science solution.
* Develop and communicate recommendations and data science solutions in easy-to-understand-way leveraging data to tell a story.
* Lead and persuade others while positively influencing the outcome of team efforts and help frame a business problem into a technical problem resulting in a feasible solution.
Required Qualifications, Capabilities, and Skills
* Master's Degree with 5+ years or Doctorate (PhD) with 3+ years of experience operating as an data science professional (e.g. data scientist, statistician, or related professions) in a quantitative field: Statistics, Analytics, Data Science, Engineering, Operations Research, Economics, Mathematics, Machine Learning, Artificial Intelligence, and related disciplines.
* 2+ years of experience leading AI/ML projects with multiple team members
* Hands-on experience developing statistical models, machine learning models, and/or artificial intelligence models.
* Deep understanding of math and theory behind AI/ML algorithms.
* Proficient in data science programming languages like Python, R or Scala.
* Experience with big-data technologies such as Hadoop, Spark, SparkML, etc. & familiarity with basic data table operations (SQL, Hive, etc.).
* Demonstrated relationship building skills, with a superior ability to make things happen through the use of positive influence.
Preferred Qualifications, Capabilities, and Skills
* Advanced expertise with Time Series and Operations Research techniques.
* Natural Language Processing(NLP)/Natural Language Generation(NLG), Neural Nets, or other ML/AI skills.
* Prior experience with public cloud technologies such as Amazon Web Services(AWS), Azure or Google Cloud Platform(GCP).
* Previous experience leading highly complex cross-functional technical projects with multiple stakeholders
This position is full time in office Monday - Friday. This position is not hybrid nor remote.
Auto-ApplyR&D Associate Scientist II
Associate principal scientist job in New Albany, OH
Nature and Scope Responsible for formulation and process development activities associated with parenteral drug product development. Participates in scale-up of manufacturing process. Essential Duties and Responsibilities Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time.
* Conduct laboratory experiments with minimal supervision to support formulation and process development of injectables Execute laboratory studies for characterization, stability studies per ICH guidelines, component selection and scale-up activities Execute and support the formulation team on experiments to support the selection of process parameters and development of manufacturing process.
* Prepare formulations to support analytical method development.
* Draft protocols/reports on the formulation development experiments and deliver data presentations.
* Assist in the general operation of the R & D formulation laboratory including maintenance of Standard Operating Procedures (SOP's) and equipment validation or maintenance.
* Maintain clean and safe work environment in the laboratory.
* Ensure all work is performed and documented in accordance with existing company policies, procedures, current Good Manufacturing Practices, and health & safety requirements.
* Perform any other tasks/duties as assigned by management.
Education Requirements and Qualifications
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required.
* B.S. in Pharmaceutical Science, Chemistry, Chemical Engineering or equivalent required.
* 2-3 years, or for M.S. 0-2 year, of experience in drug product development required.
* Hands on skills in analytical instrumentals such as HPLC, particle sizer and Karl Fisher titrator is a plus.
* Excellent organizational, interpersonal and communication skills required.
* Proficiency in Microsoft Office Word and Excel is required.
* Ability to work overtime as needed.
Physical Environment and Requirements
* Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves. PPE and Respirators are essential for the health and safety of employees.
* Specific vision requirements include 20/20 near vision (can be corrected with eyeglasses or contacts) and color vision.
* Position requires working in the laboratory as well as sitting.
Employees must maintain a clean-shaven appearance each working shift to wear tight-fitting respirators properly.
American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status.
Applicants have rights under Federal Employment Laws.
* FMLA poster: **********************************************************
* Know Your Rights: Know Your Rights: Workplace discrimination is illegal (eeoc.gov)
* Employee Polygraph Protection Act: *********************************************************
Alert: We're aware of individuals impersonating our staff to target job seekers. Please note:
* All legitimate communication will come directly from a verified ARI recruiter either by phone or via an americanregent.com email address.
* Our recruiting process includes multiple in person and/or video interviews and assessments.
* If you are unsure about the legitimacy of a message, contact John Rossini at *************************** before responding.
* We never request payment, bank information, or personal financial details during our offer process.
Your security is important to us, and we encourage you to stay vigilant when job searching.
American Regent Inc. endeavors to make *********************************** accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please email **************************************.
Auto-ApplyProcess & Formulation Scientist
Associate principal scientist job in Marysville, OH
Here at Scotts Miracle-Gro there is no such thing as a typical day. Our culture is constantly energized by new and exciting growth opportunities and at a rapid pace. Below are details on an open job. If the role interests you and you would like to be considered we encourage you to apply!
We are looking for a Process & Formulation Scientist who will join our team.
We are seeking a creative and motivated Process & Formulation Scientist or Engineer to join the Research & Development Innovation Team. This role will focus on the design, development and characterization of novel products and formulations for the consumer lawn and garden category for Scotts Miracle-Gro. Key responsibilities include identifying and evaluating new and emerging technologies to validate functionality, efficacy and commercialization viability to advance the key innovation focus areas for multiple business units. The Scientist/Engineer will contribute to the development of our strategy by providing expertise as a project champion and thought leader. The Scientist/Engineer will align technologies with consumer and business needs, work cross functionally with the innovation team and business unit partners to advance the technologies to the next phase of development. We are highly focused on three major categories: biologicals, environmental stewardship, including alternative and natural fertilizers, novel biodegradable polymer and films, sustainable and renewable materials ; novel non-synthetic active ingredients and co-formulants that are safe, effective, or more efficient for use in residential pesticides and plant growth promoting products ; as well as integrated technology such as smart devices and controllers.
In this role you will:
• Identifying new technologies and opportunities that meet company objectives and strategies and support the development, refinement and scale up to commercial launch. This includes following and adhering to state and federal regulation requirements such as OMRI, OIM and FIFRA.
• Document, analyze and report data to cross-functional teams, peers, and leadership making recommendations on path forward to multiple business units.
• Collaborate closely with innovation team, subject matter experts and business unit partners to ensure alignment on project goals and maximize efficient use of resources versus milestones and commercialization schedules.
• Provide technical support and advice to cross functional partners for new and current products and technologies.
• Coaches and develops the technical skills of peer or junior associates. Assists with identifying career development opportunities and developing a succession plan.
What you'll need to be successful:
• Master's Degree, Chemistry, Chemical Engineering, Microbiology, Biologicals, Biopolymers, Biomaterials, or related field
• 2 - 4 Years of experience prefered
• Years of experience required may vary based on the highest level of education completed. Example: Bachelor's degree with 4-7 years of qualified experience, Master's Degree with 2-4 Year of qualified experience, and Ph.D with a 0-2 year of relevant experience
Skills
Scientific curiosity and rigor | Motivated to identify opportunities and increase their overall contributions | Attention to detail | Accuracy | Laboratory skills
Networking skills | Excellent written and oral communication skills | Adaptability and flexibility to work independently as well as in a team environment
Computer skills - spreadsheets, presentations, documents, data analysis, etc | Relationship building | Self- Starter that's action oriented | Quality results oriented
The starting budgeted pay range for this role will generally fall between $77,200.00 - $90,800.00 per year. Scotts will consider various factors in determining the actual pay including your skills, qualifications, experience, and geographical location.In addition to the determined base salary, this role is also incentive eligible under our corporate bonus programs.For remote roles where the final candidate resides in Alaska, California, Colorado, Illinois, New York, Oregon or Washington, state required pay thresholds will be factored into base salary.
Here at ScottsMiracle-Gro, we believe providing an enriching and engaging employee experience is what sets us apart from other organizations. We recognize our employees are so much more than just their job title so we offer programs and benefits that support them in all aspects of their lives. Wondering how we do it? Below is a glimpse of our highlight reel…
Our
Live Total Health
program provides you with options to align to your personal needs. Selections range from medical, dental and vision coverage for you, your spouse/domestic partner and dependents to an outstanding wellness reimbursement program to an unbelievable 401K match (up to 7.5%) as well as a 15% discount on company stock and much more
We know our talent is our most precious asset and your unique development contributes to our organization's success now and in the future. Career growth at our company is not always a ladder. It's much more like a rock climbing adventure. Grow through exploration and experiences rather than a predictable linear path.
We value the importance of family. We provide access to Maven Family Planning and up to $30,000 to accommodate for adoption, fertility and surrogacy.
Be part of something bigger by joining one of our Employee Resource Groups focusing on diversity and inclusion, family, education and sustainability: Scotts Women's Network, Scotts Black Employees' Network, Scotts Veterans Network, Scotts Young Professionals, Scotts Pride Network (GroPride), Scotts Associates for a Greener Earth (SAGE), Scotts Family TREE and our Associate Boards.
Join a company with a strong belief in giving back to the communities where we live and work. We have a shared passion for service and volunteerism and believe participating in community service benefits our communities and strengthens our team.
Not interested in this role? Stay up to date on future opportunities by joining our ScottsMiracle-Gro and Hawthorne Gardening talent communities.
Scotts is an EEO Employer, dedicated to a culturally diverse, drug free workplace.
EEO/AA Employer/Minority/Female/Disability/Veteran/Sexual Orientation/Gender Identity
Notification to Agencies:
Please note that the Scotts Miracle-Gro company does not accept unsolicited resumes from recruiters or employment agencies. In the absence of a signed Master Service Agreement, and specific approval to submit resumes to an approved requisition, the Scotts Miracle-Gro company will not consider or approve payment regarding recruiter fees or referral compensations.
Auto-ApplyPharmacovigilance Scientist
Remote associate principal scientist job
Axsome Therapeutics is a biopharmaceutical company leading a new era in the treatment of central nervous system (CNS) conditions. We deliver scientific breakthroughs by identifying critical gaps in care and develop differentiated products with a focus on novel mechanisms of action that enable meaningful advancements in patient outcomes. Our industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, and multiple late-stage development programs addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Together, we are on a mission to solve some of the brain's biggest problems so patients and their loved ones can flourish. For more information, please visit us at ************** and follow us on LinkedIn and X.
About This Role
Axsome Therapeutics is seeking a Pharmacovigilance Scientist to establish and execute pharmacovigilance (PV) systems and procedures, with a strong focus on maintaining high-quality standards. This role is responsible for supporting the Pharmacovigilance (PV) Science function under the guidance of the PV physician and providing oversight of ICSR assessment, signal detection, medical surveillance and risk management activities for investigational products in clinical development and marketed products. This position collaborates with key internal stakeholders, including Clinical Development, Commercial, Medical Information, Medical Affairs, Quality, Regulatory and Legal, as well as multiple external Service Providers and partners on pharmacovigilance-related matters.
This position reports to Executive Director of Pharmacovigilance/Drug Safety and is based at Axsome's HQ in New York City with an on-site requirement of at least three days per week. We are unable to consider candidates who are looking for fully remote roles.
Job Responsibilities and Duties include, but are not limited to, the following:
Assist safety physician to enhance safety surveillance and signal detection by monitoring and analyzing safety data from various sources to identify potential safety signals or trends related to investigational and marketed products
Contribute to the creation and execution of risk minimization measures to mitigate identified risks.
Support the preparation pharmacovigilance aggregate safety reports (e.g., PADER, PSURs, DSURs) to regulatory authorities to meet compliance requirements.
Collaborate with PV physician/PV operations and key stakeholders to request/receive applicable sections of the report
Provide training and guidance to other functions to address ad hoc questions and issues
Ensure timely finalization of the reports to meet the submission timelines of relevant health authorities and other external stakeholders
Collaborate and communicate with cross-functional teams to ensure effective safety monitoring and communication
Support the safety review team (SRT) and coordinates all safety topic discussion and documentation.
Ensure appropriate stakeholder representation and input at SRT
Ensure all data is appropriately compiled and presented at SRT for team review
Liaise with SRT chair to facilitate communication and support for decisions resulting from the SRT (e.g. update of RMPs, labeling, regulatory notifications etc.)
Contribute to clinical trials by providing safety input and reviewing documents such as Clinical Study Reports (CSRs), protocols, and investigator brochures (IB), ICF etc.
Provide support for the processing of individual case safety reports (ICSRs) and ensure data accuracy and completeness for investigational and marketed products
Support the PV SOP updates
Oversee vendor safety process, e.g., signal detection, validation and assessment.
Participate in audit/inspection preparedness activities and provide support during regulatory inspections in collaboration with team members
Participate in new study initiation to ensure PV requirements are met including but not limited to safety reporting, query resolution, SAR reconciliation, un-blinding process, and safety reporting training
Evaluate and improve current PV processes, as needed, to strengthen medical surveillance and risk management process ensuring alignment with best practices
Requirements / Qualifications
Master's degree in health-discipline or equivalent required, RN, R.Ph, or Pharm D degree is highly preferred
5+ years of progressively responsible Pharmacovigilance experience in a pharmaceutical, biotechnology, or related environment with focused experience in signal detection, safety surveillance, risk mitigation and risk management
Extensive experience in case processing, regulatory requirements of ICSRs, MedDRA, WHODD, project management
Experience in submission activities in both FDA and EU is preferred, but not required
Must demonstrate the ability to draft reports, business correspondence, and procedures, and to effectively present information and respond to questions from internal and external stakeholders, both domestic and international
Ability to work on site Monday, Tuesday & Thursday. We are unable to consider candidates who are looking for fully remote roles.
Experience and Knowledge
Knowledge of ICH E2B(R2) and (R3) specifications and entry guidance.
Knowledge of global pharmacovigilance reporting rules and timelines, including but not limited to Health Canada, FDA and EMA.
Knowledge of relevant food and drug administration (FDA), European union (EU) and international conference on Harmonization (ICH) guidelines, initiatives, and regulations governing pharmacovigilance.
Ability to interpret health and medical records such as adverse event reporting forms, a discharge summary, etc.
Experience with clinical and/or post-marketing case assessment, including medical terminologies, MedDRA and WHO DD coding and narrative writing.
Experience with safety database is required; ARISg is a plus but not mandatory.
Experience with Veeva is a plus but not mandatory.
Ability to work independently and collaboratively, as required, in a fast-paced matrixed team environment consisting of internal and external team members
Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines
Ability to read, analyze, and interpret professional journals, technical procedures, and governmental regulations
Excellent planning, organization, and time management skills including the ability to support and prioritize multiple projects
Excellent verbal and written communication and skills
Excellent in detailed-oriented tasks.
Salary & Benefits
The anticipated salary range for this role is $150,000 - $185,000. We encourage candidates of all levels to apply as there may be flexibility on final job title and responsibilities. The salary offer will be based on a variety of factors, including experience, qualifications, internal equity and location. Axsome offers a competitive employment package that includes an annual bonus, significant equity and a generous benefits package.
Axsome is committed to equal employment opportunity and providing reasonable accommodations to applicants with physical and/or mental disabilities. We value and encourage diversity and solicit applications from all qualified applicants without regard to race, color, gender, sex, age, religion, creed, national origin, sexual orientation, gender identity, ancestry, citizenship, marital status, physical or mental disability, medical condition, veteran status, genetic information, or any other characteristic protected by federal, state, or local law.
Axsome Therapeutics does not accept unsolicited resumes from recruiters or third-party recruitment agencies and will not pay placement fees for unsolicited candidates that are sent to hiring managers, the HR team or other Axsome team members. Only approved vendors who have been explicitly asked to support a specific search will receive access to our Applicant Tracking System to submit candidates for consideration.
Auto-ApplyResearch Scientist II
Remote associate principal scientist job
See yourself at Dataminr
As an AI Research Scientist you'll be working on some of the most challenging AI problems in real-time event detection and directly contributing to products while advancing the state of the art. This role can be remote or based out of our New York City, Dublin, or London offices.
AI Innovation at Dataminr
Working at Dataminr you'll have the opportunity to tackle the most exciting trends in AI on a daily basis to power a revolutionary product that uncovers critical events around the world as they unfold.
Regenerative AI: our AI technology, ReGenAI, is a new form of generative AI that automatically regenerates real-time Live Event Briefs as events unfold. Learn more here.
Agentic AI: we recently launched our Agentic AI capability, what we're calling our Intel Agents, that autonomously generates critical context for our clients on real-time events, threats, and risks allowing them to see the clearest, most accurate view of what's happening on the ground. Learn more here
Multimodal AI: our platform detects events from many different types of data (images, video, sensor data, audio, and text in over 150 languages). Learn more here.
The opportunity
Perform research to advance the state of the art and solve specific problems at scale in one or more of the following areas: Natural Language Processing, Machine and Deep Learning.
Work closely with a diverse, interdisciplinary team to deliver value to customers (existing and new products).
Contribute to the research community via publications in top tier venues, participation in program committees, etc.
Excel in placing a human-centered focus on the work (context, end-user impact, etc), finding solutions that work in practice and have significant impact.
Productionize and ship research into Dataminr's products, and thus to its users worldwide.
Senior candidates are expected to lead technical areas and/or people.
What you bring
At Dataminr, we value you for who you are. We encourage you to apply for this role, even if you don't meet every qualification. Our candidates are reviewed on the basis of their skill and potential to succeed.
Ph.D. in Computer Science or related field
Experience in one or more of the following topics: AI for cyber security, LLMs, agentic AI, generation, machine translation, summarization, topic detection & tracking, text classification, knowledge extraction/representation/management, trending topic detection, search, machine learning and deep learning, etc.
Outstanding publication record (IEEE, AAAI, NeurIPS, ACL, TACL, EMNLP, WWW, etc.).
Demonstrated ability to work independently, set up experiments and demonstrate progress through principled use of metrics.
Proficiency in Python and experience with relevant AI/ML libraries and frameworks such as PyTorch and Hugging Face Transformers. Experience with LLM serving technologies such as vLLM is a plus.
Professional experience in industry (requirement varies depending on level; recent graduates must have had relevant internships).
#LI-Remote
#LI-BM
About Dataminr
At Dataminr, we are a mission driven team of talented builders, creators and visionaries who have real-world impact on how organizations are able to respond to events. Dataminr's groundbreaking, AI-powered, intelligence platform provides organizations with the earliest signals of emerging risks, events, and threats before they unfold. Trusted by two-thirds of the Fortune 50 and half of the Fortune 100, Dataminr's platform analyzes billions of public data inputs spanning text, image, video, audio and sensor data across 150+ languages, empowering our clients to stay one step ahead in an increasingly complex world where every second counts.
Founded in 2009, we have pioneered the world's first real-time event detection platform, long before the recent Gen AI ‘boom.' Dataminr operates all around the world united by our passion to use AI for the greater good, be agents of positive change and put our technology into the hands of clients charged with the responsibility to keep organizations running and keep people safe.
As our employees focus on developing our revolutionary technology, we focus on our employees. Dataminr is proud to offer a variety of flexible work arrangements, offices all over the world to foster collaboration, generous PTO and sick leave, and more, as part of our competitive benefits package aimed at keeping all our employees happy and healthy. Explore all our benefits here.
We believe our differences give us strength. Our employees are empowered to be their best, authentic selves through various opportunities, such as our robust employee resource group (ERG) network, manager development programming, professional development funds, and more.
We serve a global community made up of many cultures and strive to reflect the world and clients we serve, with a workforce built on merit and equity. We actively condemn racism and discrimination in any form. We stand for social good, fostering a culture of allyship, and standing up for those who face systemic barriers to equality. We lead with empathy and strive to be agents of positive change in our company and in our communities.
The annual base salary range for this position is $148,240 - $218,000. You will also be eligible to receive a discretionary bonus and Company equity. Actual salary will be based on a number of factors including, but not limited to, geographic location, applicant skills, and prior relevant experience.
Dataminr is an equal opportunity and affirmative action employer. Individuals seeking employment at Dataminr are considered without regards to race, sex, color, creed, religion, national origin, age, disability, genetics, marital status, pregnancy, unemployment status, sexual orientation, citizenship status or veteran status.
Dataminr will collect and process your personal data. All personal data will be processed in accordance with applicable data protection laws. Please see Dataminr's candidate privacy notice available here. By providing your details and applying via our careers website, you acknowledge that you have read our candidate privacy notice. If you have any queries, please contact the People Team at *************** or
privacy@dataminr.com
.
Auto-Apply