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.
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.
Sumitomo Pharma America (SMPA) endeavors to make its application process accessible to all. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact SMPA at **********************************************
This contact information is for accommodation requests only and cannot be used to inquire about the status of applications.
At Sumitomo Pharma America, our work is guided by the Sumitomo Pharma mission, vision and values, which tie closely to our company's cultural pillars.
**Our** **Mission**
_To broadly contribute to society through value creation based on innovative research and development activities for the betterment of healthcare and fuller lives of people_ _worldwide_
**Our** **Vision**
_For Longer and Healthier Lives, we unlock the future with cutting edge technology and_ _ideas_
$102k-127k yearly 60d+ ago
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Research Scientist - CTRL Labs
Meta 4.8
Scientist job in Montpelier, VT
Reality Labs at Meta is seeking Research Scientists with experience in product-focused machine learning and signal processing research to advance our pioneering work in neuromotor interfaces, which has grown out of the acquisition of CTRL-labs. We're building a practical interface drawing on the rich neuromotor signals that can be measured non-invasively via surface electromyography (EMG) with single motor neuron resolution. This technology could become one of the main pillars for interaction with virtual and augmented worlds.We are a multi-disciplinary team of researchers investigating the nature of human neuromotor signals, developing novel signal processing and machine learning methods to infer a user's intent, and creating novel interaction techniques and user experiences. Help us unleash human potential by removing the bottlenecks between user intent and action.
**Required Skills:**
Research Scientist - CTRL Labs Responsibilities:
1. Research and develop Deep Learning or other computational models
2. Design methods, tools and infrastructure to analyze and leverage rich multimodal data sets
3. Set technical direction for a project of 2-3 researchers and engineers
4. Help transition and deliver our work from research into product
5. Adapt standard machine learning methods to best leverage modern parallel environments (e.g. distributed clusters, multicore SMP, and GPU)
**Minimum Qualifications:**
Minimum Qualifications:
6. Bachelor's degree in Computer Science, Computer Engineering, relevant technical field, or equivalent practical experience
7. Ph.D. degree in Computer Science and Engineering, Electrical Engineering, Statistics/Mathematics
8. Experience with developing machine learning models at scale from inception to business impact
9. Programming experience in Python and hands-on experience with frameworks such as PyTorch
10. Exposure to architectural patterns of large scale software applications
11. Must obtain work authorization in the country of employment at the time of hire, and maintain ongoing work authorization during employment
**Preferred Qualifications:**
Preferred Qualifications:
12. Proven track record of achieving significant results as demonstrated by grants, fellowships, patents, as well as first-authored publications at peer-reviewed AI conferences (e.g. NeurIPS, CVPR, ICML, ICLR, ICCV, ACL, and ICASSP)
13. Demonstrated software engineer experience via an internship, work experience, coding competitions, or widely used contributions in open source repositories (e.g. GitHub)
14. Experience bringing machine learning-based products from research to production
**Public Compensation:**
$184,000/year to $257,000/year + benefits
**Industry:** Internet
**Equal Opportunity:**
Meta is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state and local law. Meta participates in the E-Verify program in certain locations, as required by law. Please note that Meta may leverage artificial intelligence and machine learning technologies in connection with applications for employment.
Meta is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know at accommodations-ext@fb.com.
$184k-257k yearly 60d+ ago
Applied Scientist 4
Oracle 4.6
Scientist job in Montpelier, VT
Invent, implement and deploy state-of-the-art machine learning and/or specific domain industry algorithms and systems. Build prototypes and explore conceptually new solutions. Work collaboratively with science, engineering, and product teams to identify customer needs in order to create and implement solutions, promote innovation and drive model implementations. Applies data science capabilities and research findings to create and implement solutions to scale. Responsible for developing new intelligence around core products and services through applied research on behalf of our customers. Develops models, prototypes, and experiments that pave the way for innovative products and services. Build cloud services that work out of the box for enterprises, e.g. decision support, anomaly detection, forecasting and recommendations), natural language processing (NLP), Natural Language Understanding (NLU),Time Series, Automatic Speech Recognition (ASR), Machine Learning (ML), and Computer Vision (CV). Design and run experiments, research new algorithms, and find new ways of optimizing risk, profitability, and customer experience. Conversant on ethical problems in consideration of sciences.
**Responsibilities**
Leading contributor providing guidance and mentorship to define, design and deliver product quality improvements from ideation stage to shipping to the customer. Write high quality code to power experiments and build models. Contributes to writing production model code. Work closely with product management and engineering to deliver products which solves the needs of our customers by building relevant, innovative results which strategically differentiates Oracle in the market. Set up environment needed to run experiments for all projects. Set up distributed environments. Engage with customers and help solve complex problems with the customer/partner. Directly impact our customers via innovation in products and services that make use of ML/AI technology. Clearly articulate technical work to audiences of all levels and across multiple functional areas. Keep track of the progress and ensure the team is following the best practices. Works on training data collection, feature engineering, model training, offline and online experimentation. Drives independent research and development. Advance the state-of-the-art machine learning and algorithms for real-world large-scale applications. Ensure solutions are designed with fairness and explainability in mind. May perform other duties as assigned.
Disclaimer:
**Certain US customer or client-facing roles may be required to comply with applicable requirements, such as immunization and occupational health mandates.**
**Range and benefit information provided in this posting are specific to the stated locations only**
US: Hiring Range in USD from: $120,100 to $251,600 per annum. May be eligible for bonus, equity, and compensation deferral.
Oracle maintains broad salary ranges for its roles in order to account for variations in knowledge, skills, experience, market conditions and locations, as well as reflect Oracle's differing products, industries and lines of business.
Candidates are typically placed into the range based on the preceding factors as well as internal peer equity.
Oracle US offers a comprehensive benefits package which includes the following:
1. Medical, dental, and vision insurance, including expert medical opinion
2. Short term disability and long term disability
3. Life insurance and AD&D
4. Supplemental life insurance (Employee/Spouse/Child)
5. Health care and dependent care Flexible Spending Accounts
6. Pre-tax commuter and parking benefits
7. 401(k) Savings and Investment Plan with company match
8. Paid time off: Flexible Vacation is provided to all eligible employees assigned to a salaried (non-overtime eligible) position. Accrued Vacation is provided to all other employees eligible for vacation benefits. For employees working at least 35 hours per week, the vacation accrual rate is 13 days annually for the first three years of employment and 18 days annually for subsequent years of employment. Vacation accrual is prorated for employees working between 20 and 34 hours per week. Employees working fewer than 20 hours per week are not eligible for vacation.
9. 11 paid holidays
10. Paid sick leave: 72 hours of paid sick leave upon date of hire. Refreshes each calendar year. Unused balance will carry over each year up to a maximum cap of 112 hours.
11. Paid parental leave
12. Adoption assistance
13. Employee Stock Purchase Plan
14. Financial planning and group legal
15. Voluntary benefits including auto, homeowner and pet insurance
The role will generally accept applications for at least three calendar days from the posting date or as long as the job remains posted.
Career Level - IC4
**About Us**
As a world leader in cloud solutions, Oracle uses tomorrow's technology to tackle today's challenges. We've partnered with industry-leaders in almost every sector-and continue to thrive after 40+ years of change by operating with integrity.
We know that true innovation starts when everyone is empowered to contribute. That's why we're committed to growing an inclusive workforce that promotes opportunities for all.
Oracle careers open the door to global opportunities where work-life balance flourishes. We offer competitive benefits based on parity and consistency and support our people with flexible medical, life insurance, and retirement options. We also encourage employees to give back to their communities through our volunteer programs.
We're committed to including people with disabilities at all stages of the employment process. If you require accessibility assistance or accommodation for a disability at any point, let us know by emailing accommodation-request_************* or by calling *************** in the United States.
Oracle is an Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability and protected veterans' status, or any other characteristic protected by law. Oracle will consider for employment qualified applicants with arrest and conviction records pursuant to applicable law.
$69k-96k yearly est. 60d+ ago
Scientist III - Microbiologist, EM Focus, Analytical Sciences Microbiology - FSP
Parexel 4.5
Scientist job in Montpelier, VT
We are looking to fill a microbiologist position (environmental monitoring focus) working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients in Rahway, NJ. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer sponsorship.
**Qualifications**
+ Bachelor's degree required; concentration in a scientific or applied discipline strongly preferred
+ A minimum of two years of experience in pharmaceutical microbiology related position required (occasional overtime)
**Required Skills and Experience**
+ Experience in working in a GMP Pharmaceutical environment with specific experience environmental monitoring
+ Proven technical writing skills (SOPs, protocols)
**Responsibilities**
ENVIRONMENTAL MONITORING
+ Proficiency in the pharmaceutical microbiology laboratory workflow for EM collection and testing, reporting and trending
+ Sampling EM rooms, surface and air
+ Collection and testing water samples
+ Weekly water trends- visually to be able to report back to the source area
+ Equipment responsibilities with metrology oversight, automation, etc
+ MODA USE
+ Responsible for writing annual reports
+ Responsible for writing trend reports
+ Able to clearly interpret adverse vs desirable data
+ Mold investigations and studies
+ PSIM work
+ Biological indicator analysis and certification
+ Disinfection studies where appropriate
+ Critical thinking with data
MICROBIOLOGICAL PRODUCT ANALYSIS
+ Analyze samples and compile meaningful data
+ Perform Investigations and prepare/respond to CAPA
+ Review, revise Test Procedures/Standard Operating Procedures
+ Ad Hoc work
+ Rotational on-call assignments for responding to alarms
MICROBIOLOGICAL ACTIVITIES Include (but not limited to):
+ Receive, verify & Log in samples
+ Return templates and shipping paperwork when and where appropriate
+ Prepare and ship materials offsite for ID/testing (when applicable)
+ Stock culture management and quality control of same
+ Biological indicator management
+ Bioburden testing
+ Water sampling
+ Microbiological media management and quality control of same
+ Sterilization activities
+ Research experiments as deemed appropriate by client management
+ Method Validation/Qualification
+ Other microbiological activities
CALIBRATIONS:
+ Execute "Before-Use" calibrations prior to performing testing
+ Review calibration data within the ELN
+ Prepare and submit equipment for calibrations (offsite or onsite)
+ Complete calibration/PM paperwork
GMP ACTIVITIES:
+ Prepare GMP documentation as requested by management
+ Perform laboratory sanitizations and ensure cleanliness of laboratory workspace
+ Perform equipment sanitizations (incubators / hoods / refrigerators)
+ Purchase supplies (GMP)
+ Prepare and send documents to Records Center
INVESTIGATIONS:
+ Initiate, facilitate, and perform Investigations and NOEs (Notice of Event-NOE) for Environmental samples [NOE for Microbiological Environment Event (MEN)]
+ Inform management of non-conforming events
AUDITS:
+ Participate in audits (Regulatory, In-house, Corporate)
+ Participate in self-inspections and safety inspections
+ Retrieve data when requested by Microbiology management
TRAINING:
+ Complete assigned training when required
+ Ensure training is complete prior to performing tasks
+ The role is intended to be a 40-hour-per-week position.
**About Parexel**
Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies.
For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement.
Come join us!
\#LI-DK1
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
$78k-101k yearly est. 18d ago
Associate R & D Data Scientist
Educational Testing Service 4.4
Scientist job in Montpelier, VT
**About ETS:** ETS is a global education and talent solutions organization enabling lifelong learners worldwide to be future-ready. For more than 75 years, we've been advancing the science of measurement to build benchmarks for fair and valid skill assessment across cultures and borders. Our worldwide impact extends through our renowned assessments including TOEFL , TOEIC , GRE and Praxis tests, serving millions of learners in more than 200 countries and territories. Through strategic acquisitions, we've expanded our global capabilities: PSI strengthens our workforce assessment solutions, while Edusoft, Kira Talent, Pipplet, Vericant, and Wheebox enhance our educational technology and assessment platforms across critical markets worldwide.
Through ETS Research Institute and ETS Solutions, we're partnering with educational institutions, governments, and organizations globally to promote skill proficiency, empower upward mobility, and unlock opportunities for everyone, everywhere. With offices and partners across Asia, Europe, the Middle East, Africa, and the Americas, we deliver nearly 50 million tests annually. Join us in our journey of measuring progress to power human progress worldwide.
The Associate R&D Data Scientist contributes to the planning, development, and execution of data science analyses for research and development projects within the ETS Research Institute. This role focuses on applying advanced data science, statistics, machine learning, and AI to make inferences and/or predictions from data. The position requires expertise in modern frameworks and cloud computing environments to support innovative research in educational measurement and assessment.
**Primary Responsibilities**
_Technical Responsibilties:_
Data Management and Analysis
+ Collect, preprocess, and manage structured and unstructured data from diverse sources, ensuring data quality and integrity.
+ Perform exploratory data analysis to identify trends, patterns, and actionable insights.
Model Development and Evaluation
+ Design, implement, and validate predictive models and machine-learning algorithms using frameworks such as PyTorch/TensorFlow, and scikit-learn.
+ Experiment with large language models and generative AI techniques (e.g., working with large language model APIs, prompt engineering) to support innovative research.
Deployment and Scalability
+ Develop and maintain pipelines for model deployment in cloud computing environments (e.g., AWS, Azure) to ensure scalability and reproducibility.
_Research and Collaboration_
+ Collaborate with scientists and cross-functional research teams to align data science efforts with program objectives
+ Contribute to technical reports, presentations, and publications that disseminate research findings.
+ Communicate complex technical concepts clearly to both technical and non-technical stakeholders.
\#LI-MM1
\#Remote
+ Demonstrable proficiency and experience in Python and/or R for data analysis and modeling.
+ Hands-on experience with PyTorch/TensorFlow, Scikit-learn, and other machine learning frameworks.
+ Familiarity with generative AI methods and their practical applications.
+ Strong understanding of statistical methods, experimental design, and data visualization.
+ Ability to work in cloud computing environments (e.g., AWS) for model deployment and data processing.
+ Excellent problem-solving skills and adaptability to evolving research priorities.
+ Effective written and verbal communication skills for collaborative research environments.
+ Exceptional attention to detail, ensuring accuracy and reliability in data analysis, modeling, and reporting.
**Education:**
Master's degree in Data Science, Computer Science, Statistics, or a related quantitative field; or equivalent combination of education and experience.
**ETS is mission driven and action oriented**
+ We are passionate about hiring innovative thinkers who believe in the promise of education and lifelong learning.
+ We are energized by cultivating growth, innovation, and continuous transformation for the next generation of rising professionals as leaders. In support of this ETS offers multiple Business Resource Groups (BRG) for you to learn and advance your career growth!
+ As a not-for-profit organization we will encourage you to lean in to your passion for volunteering. At ETS you may qualify for up to an additional 8 hours of PTO for volunteer work on causes that are important to you!
+ The base salary range advertised represents the low and high end of the anticipated salary range for this position. The base pay actually offered will take into account internal equity and also may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors. The base pay is only one aspect of the Total Rewards Package that will be offered to the successful candidate.
**ETS is an Equal Opportunity Employer. We are committed to providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, marital status, veteran status, sexual orientation, gender identity, or any other characteristic protected by law. We believe in creating a work environment where all individuals are treated with respect and dignity.**
$75k-98k yearly est. 17d ago
Senior AI/ML Scientist
General Motors 4.6
Scientist job in Montpelier, VT
**The Role:** General Motors is seeking a **Senior AI/ML Scientist** to join the Vehicle Mechatronic Embedded Controls (VMEC) organization. In this role, you will design and deploy advanced machine learning solutions that drive innovation across vehicle lifecycle management, diagnostics, and predictive maintenance. You will work on cutting-edge AI technologies, including large language models (LLMs), generative AI, and real-time inference systems, to enable intelligent, scalable solutions for automotive applications.
**What You'll do:**
+ Develop and deploy production-grade ML models and AI systems for diagnostics, predictive maintenance, and anomaly detection supporting product health.
+ Build and optimize LLM-based applications, including Retrieval-Augmented Generation (RAG) systems for technical documentation and automated analysis.
+ Implement predictive models for failure detection, remaining useful life, and early warnings.
+ Apply advanced ML techniques such as deep learning, NLP, time-series forecasting, and generative AI.
+ Create scalable data pipelines and real-time inference systems.
+ Collaborate with cross-functional teams and mentor junior engineers.
+ Present insights to both technical and non-technical stakeholders and drive adoption of ML solutions through dashboards and APIs.
**Your Skills & Abilities (Required Qualifications)**
+ Bachelor's degree in Computer Science, Engineering, or related field.
+ 5+ years of experience deploying ML models in production environments.
+ Expertise in Python and ML frameworks (PyTorch, TensorFlow).
+ Strong SQL and distributed data processing skills (Spark, Hive).
+ Real world experience with ML platforms (Databricks, MLflow, Azure ML).
+ Familiarity with cloud platforms and containerization (Docker, Kubernetes).
**What Will Give You A Competitive Edge (Preferred Skills)**
+ Master's or Ph.D. in a related field.
+ 8+ years of experience in ML solutions.
+ Deep expertise with LLMs, RAG architectures, and vector databases.
+ Knowledge of predictive maintenance, anomaly detection, and automotive diagnostics.
+ Experience with generative AI technologies and advanced NLP techniques.
**Compensation:** The compensation information is a good faith estimate only. It is based on what a successful applicant might be paid in accordance with applicable state laws. The actual base salary a successful candidate will be offered within this range will vary based on factors relevant to the position, as well as geography of the selected candidate.
**- The salary range** for this role is 128,700 and 261,300. The actual base salary a successful candidate will be offered within this range will vary based on factors relevant to the position.
**- Bonus Potential:** An incentive pay program offers payouts based on company performance, job level, and individual performance.
Benefits:
**- Benefits:** GM offers a variety of health and wellbeing benefit programs. Benefit options include medical, dental, vision, Health Savings Account, Flexible Spending Accounts, retirement savings plan, sickness and accident benefits, life insurance, paid vacation & holidays, tuition assistance programs, employee assistance program, GM vehicle discounts and more.
GM does not provide immigration-related sponsorship for this role. Do not apply for this role if you will need GM immigration sponsorship now or in the future. This includes direct company sponsorship, entry of GM as the immigration employer of record on a government form, and any work authorization requiring a written submission or other immigration support from the company (e.g., H1-B, OPT, STEM OPT, CPT, TN, J-1, etc).
This role is based remotely, but if the selected candidate lives within a specific mile radius of a GM hub, they will be expected to report to the location three times a week {or other frequency dictated by your manager}.
This job is not eligible for relocation benefits. Any relocation costs would be the responsibility of the selected candidate.
**About GM**
Our vision is a world with Zero Crashes, Zero Emissions and Zero Congestion and we embrace the responsibility to lead the change that will make our world better, safer and more equitable for all.
**Why Join Us**
We believe we all must make a choice every day - individually and collectively - to drive meaningful change through our words, our deeds and our culture. Every day, we want every employee to feel they belong to one General Motors team.
**Benefits Overview**
From day one, we're looking out for your well-being-at work and at home-so you can focus on realizing your ambitions. Learn how GM supports a rewarding career that rewards you personally by visiting Total Rewards resources (************************************************************* .
**Non-Discrimination and Equal Employment Opportunities (U.S.)**
General Motors is committed to being a workplace that is not only free of unlawful discrimination, but one that genuinely fosters inclusion and belonging. We strongly believe that providing an inclusive workplace creates an environment in which our employees can thrive and develop better products for our customers.
All employment decisions are made on a non-discriminatory basis without regard to sex, race, color, national origin, citizenship status, religion, age, disability, pregnancy or maternity status, sexual orientation, gender identity, status as a veteran or protected veteran, or any other similarly protected status in accordance with federal, state and local laws.
We encourage interested candidates to review the key responsibilities and qualifications for each role and apply for any positions that match their skills and capabilities. Applicants in the recruitment process may be required, where applicable, to successfully complete a role-related assessment(s) and/or a pre-employment screening prior to beginning employment. To learn more, visit How we Hire (********************************************* .
**Accommodations**
General Motors offers opportunities to all job seekers including individuals with disabilities. If you need a reasonable accommodation to assist with your job search or application for employment, email (Careers.Accommodations@GM.com) us or call us at ************. In your email, please include a description of the specific accommodation you are requesting as well as the job title and requisition number of the position for which you are applying.
We are leading the change to make our world better, safer and more equitable for all through our actions and how we behave. Learn more about:
**Our Company (**************************************************
**Our Culture**
**How we hire (************************************************
Our diverse team of employees bring their collective passion for engineering, technology and design to deliver on our vision of a world with Zero Crashes, Zero Emissions and Zero Congestion. We are looking for adventure-seekers and imaginative thought leaders to help us transform mobility.
Explore our global locations (********************************************
We are determined to lead change for the world through technology, ingenuity and harnessing the creativity of our diverse team. Join us to help lead the change that will make our world better, safer and more equitable for all by becoming a member of GM's Talent Community (beamery.com) (*********************************************** . As a part of our Talent Community, you will receive updates about GM, open roles, career insights and more.
Please note that filling out the form below will not add you to our Talent Community automatically; you will need to use the link above. If you are seeking to apply to a specific role, we encourage you to click "Apply Now" on the job posting of interest.
The policy of General Motors is to extend opportunities to qualified applicants and employees on an equal basis regardless of an individual's age, race, color, sex, religion, national origin, disability, sexual orientation, gender identity/expression or veteran status. Additionally, General Motors is committed to being an Equal Employment Opportunity Employer and offers opportunities to all job seekers including individuals with disabilities. If you need a reasonable accommodation to assist with your job search or application for employment, email us at Careers.Accommodations@GM.com .In your email, please include a description of the specific accommodation you are requesting as well as the job title and requisition number of the position for which you are applying.
$98k-119k yearly est. 3d ago
Sr Scientist, Medical Writing
Cardinal Health 4.4
Scientist job in Montpelier, VT
**What does Clinical Affairs contribute to Cardinal Health** The Clinical Affairs function manages the clinical education, medical writing and communications, research, health care economics and patient safety while ensuring compliance with applicable regulatory and governing requirements for Cardinal Health products and services.
Medical Writing is a specialized role that creates clear, accurate, and compliant documents to communicate complex clinical and scientific data. It supports regulatory submissions, clinical research, and scientific communications by interpreting data and producing protocols, reports, regulatory dossiers, presentations, congress abstracts, and peer-reviewed publications, all in alignment with industry and regulatory standards.
**Responsibilities:**
The Senior Medical Writer will plan and develop high quality clinical documents to support Cardinal Health devices. Primary responsibilities include preparing Clinical Evaluation Reports (CERs), Post Market Plans & Reports (PMS and PMCF) as required by EU regulations. Additional responsibilities include providing input for product development and post-market sustaining core teams. Additional responsibilities may be assigned.
The Senior Medical Writer has medical writing and project management experience, a thorough understanding of research methodology and the ability to develop high-quality clinical documents. Extensive knowledge of the European medical device guidelines/regulations such as MEDDEV and MDD/MDR is required, as well as other global requirements for clinical evaluation and PMS/PMCF. The Senior Medical Writer has the ability to lead cross-functional project teams.
**Qualifications**
+ 8-12 years of experience, preferred
+ Bachelors in life science discipline; master's degree or PhD preferred or equivalent work experience.
**Additional skills:**
+ Proven experience performing literature reviews, analyzing data and communicating outputs.
+ Ability to provide thorough peer reviews of team members' documents for completeness and correctness of data analysis & regulatory requirements.
+ Experience working within a medical device or pharmaceutical organization in a Research & Development, Scientific and Medical Affairs, Clinical or Regulatory role.
+ Experience writing scientific documents for regulatory or journal submissions
+ Experience presenting scientific/clinical evidence in a written and oral manner to cross-functional teams.
+ Demonstrated ability to build positive constructive relationships with cross-functional team members
+ Demonstrated high level of personal integrity, emotional intelligence, flexibility
+ Extensive knowledge of MDD, MDR and MEDDEV requirements, along with other applicable global requirements for clinical evaluation and PMS/PMCF
+ Experience creating and performing literature searches in Embase, PubMed and Google Scholar
+ Excellent working knowledge of Microsoft Word, Excel, PowerPoint.
+ Proficient in using EndNote or other reference manager software
+ Strong data extraction and analysis skills
+ Proactive with a sense of urgency in managing job responsibilities
+ Recommends new practices, processes, metrics or models
**What is expected of you and others at this level**
+ Applies advanced knowledge and an understanding of concepts, principles and technical capabilities to manage a wide variety of projects
+ Participates in the development of policies and procedures to achieve specific goals
+ Recommends new practices, processes, metrics or models
+ Works on or may lead complex projects of large scope
+ Projects may have significant and long-term impact
+ Provides solutions that may set precedent
+ Independently determines method for completion of new projects
+ Receives guidance on overall project objectives
+ Acts as a mentor to less experienced colleagues
**Anticipated salary range** : $123,400 - $149,855
**Bonus eligible** : Yes
**Benefits** : Cardinal Health offers a wide variety of benefits and programs to support health and well-being.
+ Medical, dental and vision coverage
+ Paid time off plan
+ Health savings account (HSA)
+ 401k savings plan
+ Access to wages before pay day with my FlexPay
+ Flexible spending accounts (FSAs)
+ Short- and long-term disability coverage
+ Work-Life resources
+ Paid parental leave
+ Healthy lifestyle programs
Application window anticipated to close: 2/6/2026*if interested in opportunity, please submit application as soon as possible.
The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity.
\#LI-MP1
\#LI-remote
_Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply._
_Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal_ _Opportunity/Affirmative_ _Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law._
_To read and review this privacy notice click_ here (***************************************************************************************************************************
$123.4k-149.9k yearly 7d ago
Fish and Wildlife Scientist II
State of Vermont 4.1
Scientist job in Essex Junction, VT
The Vermont Fish & Wildlife Department (VFWD) is currently recruiting for a Fish and Wildlife Scientist II position for the Essex Junction District office. This position will work with fisheries professionals on Lake Champlain and inland ponds and streams in northwest Vermont. Work will focus on a wide variety of projects including assessment of Salmonid and Walleye fisheries on Lake Champlain, monitoring endangered Lake Sturgeon, sampling wild Brook Trout in headwater streams, and evaluating panfish populations in inland ponds
This position supports a wide range of fisheries management activities, including fieldwork, lab analysis, equipment maintenance, and data analysis and summarization. While projects are guided by supervising fisheries biologists, this role often involves independent coordination and execution. The ideal candidate will bring a solid foundation in fish biology and sampling techniques, mechanical aptitude, and strong communication and organizational skills.
Responsibilities:
* Maintain, operate, and repair fisheries equipment such as motorboats, trailers, ATVs, electrofishing units, nets, and other sampling gear.
* Lead and implement diverse field projects as directed by fisheries biologists.
* Train and supervise seasonal staff, ensuring safety protocols are followed and data is accurately collected.
* Assist with operations aboard the Department's 31-foot research vessel Dore on Lake Champlain.
* Conduct angler surveys on various district waters.
* Extract and age fish structures in accordance with established lab protocols.
* Manage purchasing, contracts, and associated administrative paperwork.
* Engage in public outreach and serve as a professional representative of the Vermont Fish & Wildlife Department.
Key Experience:
* Experience with large boat operations in large lake systems.
* Experience leading sampling crews and direct project oversight.
* Experience multi-tasking multiple projects and work requirements.
The ideal candidate will have a strong foundation in fish biology and sampling techniques, experience operating motorboats on large waterbodies, and can demonstrate mechanical aptitude for maintaining and troubleshooting field equipment. Success in this role also requires excellent organizational, communication, and interpersonal skills, along with the ability to independently plan, prioritize, and carry out complex tasks.
Who May
Stone is seeking an enthusiastic and dedicated environmental professional to join our Environmental Assessment and Remediation Services team. The successful applicant will work closely with our group of engaged professionals and a variety of partners, including project owners, responsible parties, municipalities, state and federal agencies, and other project stakeholders to lead the evaluation, design, and implementation of projects involving hazardous wastes in the environment. The candidate will serve as mentor for staff, provide senior technical support for a variety of projects at hazardous waste and brownfield redevelopment sites, and conduct business development activities. This position will report to the Director of Environmental Assessment and Remediation Services in Montpelier.
Work will involve a variety of analysis and design; preparation of engineering design calculations, drawings, and specifications; technical research and report writing; senior technical review of client deliverables, and successful identification and pursuit of project opportunities. The successful candidate will lead, direct, and review studies within their area of expertise; prepare proposal scopes of work and budgets; prepare work plans and reports, plans and specifications; prepare opinions of probable remedial and construction costs; and direct and mentor junior staff.
Requirements
Required To be considered for this position, the following skills are required:
A strong interest in brownfield redevelopment and conducting environmental site investigation and remediation projects
A proven track record in business development
Proven experience in developing project plans, anticipating, and addressing project issues, managing and mentoring staff, leading meetings with clients, and directing the completion of technical reports
Excellent verbal and written communication skills
Capacity to successfully manage multiple tasks and objectives
Legally able to work in the United States (proper documentation required)
Preferred Skills/Experience
Team or group leadership
Strategic visioning
Demonstrated ability to work with Vermont state government agencies and contract vehicles desired with direct experience with the Vermont Investigation and Remediation of Contaminated Properties Rule
Experience Level and Education
A B.S. in Environmental or Civil Engineering or related field is required.
Twelve years of relevant experience in the technical skill areas described above are required.
An advanced degree can be used in substitution for two years of experience.
$70k-91k yearly est. 60d+ ago
Data Scientist, Privacy
Datavant
Scientist job in Montpelier, VT
Datavant is a data platform company and the world's leader in health data exchange. Our vision is that every healthcare decision is powered by the right data, at the right time, in the right format. Our platform is powered by the largest, most diverse health data network in the U.S., enabling data to be secure, accessible and usable to inform better health decisions. Datavant is trusted by the world's leading life sciences companies, government agencies, and those who deliver and pay for care.
By joining Datavant today, you're stepping onto a high-performing, values-driven team. Together, we're rising to the challenge of tackling some of healthcare's most complex problems with technology-forward solutions. Datavanters bring a diversity of professional, educational and life experiences to realize our bold vision for healthcare.
As part of the Privacy Science team within Privacy Hub you will play a crucial role in ensuring that privacy of patients is safeguarded in the modern world of data sharing. As well as working on real data, you will be involved in exciting research to keep us as industry leaders in this area, and stimulating discussions on re-identification risk. You will be supported in developing/consolidating data analysis and coding skills to become proficient in the analysis of large health-related datasets.
**You Will:**
+ Critically analyze large health datasets using standard and bespoke software libraries
+ Discuss your findings and progress with internal and external stakeholders
+ Produce high quality reports which summarise your findings
+ Contribute to research activities as we explore novel and established sources of re-identification risk
**What You Will Bring to the Table:**
+ Excellent communication skills. Meticulous attention to detail in the production of comprehensive, well-presented reports
+ A good understanding of statistical probability distributions, bias, error and power as well as sampling and resampling methods
+ Seeks to understand real-world data in context rather than consider it in abstraction.
+ Familiarity or proficiency with programmable data analysis software R or Python, and the desire to develop expertise in its language
+ Application of scientific methods to practical problems through experimental design, exploratory data analysis and hypothesis testing to reach robust conclusions
+ Strong time management skills and demonstrable experience of prioritising work to meet tight deadlines
+ Initiative and ability to independently explore and research novel topics and concepts as they arise, to expand Privacy Hub's knowledge base
+ An appreciation of the need for effective methods in data privacy and security, and an awareness of the relevant legislation
+ Familiarity with Amazon Web Services cloud-based storage and computing facilities
**Bonus Points If You Have:**
+ Experience creating documents using LATEX
+ Detailed knowledge of one or more types of health information, e.g., genomics, disease, health images
+ Experience working with or supporting public sector organizations, such as federal agencies (e.g., CMS, NIH, VA, CDC), state health departments, or public health research partners. Familiarity with government data environments, procurement processes, or privacy frameworks in regulated settings is highly valued.
\#LI-BC1
We are committed to building a diverse team of Datavanters who are all responsible for stewarding a high-performance culture in which all Datavanters belong and thrive. We are proud to be an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status.
At Datavant our total rewards strategy powers a high-growth, high-performance, health technology company that rewards our employees for transforming health care through creating industry-defining data logistics products and services.
The range posted is for a given job title, which can include multiple levels. Individual rates for the same job title may differ based on their level, responsibilities, skills, and experience for a specific job.
The estimated total cash compensation range for this role is:
$104,000-$130,000 USD
To ensure the safety of patients and staff, many of our clients require post-offer health screenings and proof and/or completion of various vaccinations such as the flu shot, Tdap, COVID-19, etc. Any requests to be exempted from these requirements will be reviewed by Datavant Human Resources and determined on a case-by-case basis. Depending on the state in which you will be working, exemptions may be available on the basis of disability, medical contraindications to the vaccine or any of its components, pregnancy or pregnancy-related medical conditions, and/or religion.
This job is not eligible for employment sponsorship.
Datavant is committed to a work environment free from job discrimination. We are proud to be an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status. To learn more about our commitment, please review our EEO Commitment Statement here (************************************************** . Know Your Rights (*********************************************************************** , explore the resources available through the EEOC for more information regarding your legal rights and protections. In addition, Datavant does not and will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay.
At the end of this application, you will find a set of voluntary demographic questions. If you choose to respond, your answers will be anonymous and will help us identify areas for improvement in our recruitment process. (We can only see aggregate responses, not individual ones. In fact, we aren't even able to see whether you've responded.) Responding is entirely optional and will not affect your application or hiring process in any way.
Datavant is committed to working with and providing reasonable accommodations to individuals with physical and mental disabilities. If you need an accommodation while seeking employment, please request it here, (************************************************************** Id=**********48790029&layout Id=**********48795462) by selecting the 'Interview Accommodation Request' category. You will need your requisition ID when submitting your request, you can find instructions for locating it here (******************************************************************************************************* . Requests for reasonable accommodations will be reviewed on a case-by-case basis.
For more information about how we collect and use your data, please review our Privacy Policy (**************************************** .
$104k-130k yearly 14d ago
Embryologist
Us Fertility
Scientist job in Colchester, VT
Enjoy what you do while contributing to a company that makes a difference in people's lives. Ovation Fertility, one of the premier fertility centers in the United States, seeks experienced, compassionate, and dynamic team players who are committed to delivering exceptional patient care to join our growing practice. The work we do building families offers stimulation, challenge, and personal reward.
We have an immediate opening for an Embryologist to join our team in Colchester, Vermont. The schedule is Monday through Friday, 7:00 AM to 4:00 PM, with rotating weekends and holidays as needed. The pay range for this position is from $85,000 to $90,000 per year.
How You'll Contribute:
We always do whatever it takes, even if it isn't specifically our “job.” In general, the Embryologist is responsible for:
Undertake embryology laboratory procedures as directed
Attention to detail with an awareness and understanding of the sensitive and confidential nature of ART (Assisted Reproductive Technology) treatment
Comply with HIPAA privacy regulations
Training in latest technologies including, but not limited to: trophetoderm biopsy, oocyte vitrification, and complex micromanipulation skills
Demonstrate advanced knowledge of reproductive biology including the male and female reproductive system
Demonstrate excellent clinical skills and be able to lead and work in a team environment
Must be comfortable with the physical handling of oocytes, embryos and semen including hazardous specimens
Management of aseptic techniques
Must be competent in the correct assessment and grading of oocyte, embryo and sperm morphology
Perform clerical tasks diligently and follow established protocols and laboratory guidelines
Meticulous data entry into computer databases and software programs
Ability to maintain detailed and accurate patient logs and laboratory reports
Communicate detailed information to patients, staff and regulatory bodies
Desire to develop and coordinate clinical research projects
Develops and completes research projects which are publishable
Provides support for manuscript preparation and editing
Provides support for CAP inspection preparedness and inspections
Desire to obtain additional competency certification by the American Board of Bioanalysis
Clear, professional and timely communication with staff, physicians and patients
Participate in Continuing Technical Improvement exercises
Maintain technical proficiency in routine laboratory procedures
Assist in the preparation of routine and ad hoc analyses of data relating to performance of the laboratory and individual technologists and to specific research projects
Performs all procedures required for IVF cycles, including medium and dish preparation, egg retrieval, sperm preparation, fertilization check, embryo evaluation, cryopreservation and thawing, transfer, ICSI and assisted hatching. Experience with trophectoderm biopsy is preferred
Performs all andrology services, including preparation of semen samples for artificial inseminations and IVF, cryopreservation of sperm, and complete sperm analysis assessed by World Health Organization (WHO) standards
Performs laboratory quality control (QC), quality assessment (QA), and participates in quality improvement (QI) programs, record keeping and collection of data
Participates in research on oocytes cryopreservation, oocyte maturation, preimplantation genetic diagnosis and related research
Performs other duties as assigned, and in keeping with company policies, procedures and standards of patient care and initiatives toward continuous improvement at the individual and organizational level
Perform daily embryology (set-up's / egg retrievals / ICSI-IVF / fertilization -embryo development checks / embryo transfers / cryopreservation / testicular Bx preps-Cryo / embryo Bx for PGD) and reporting
Process semen specimens for artificial insemination/IVF-ICSI, hyaluran sperm binding assays and cryopreservation
Maintain, organize, scan and file patient results, making sure that all records are complete, including physician signatures, and accurate. Confirm results on the patient ART Summary sheets in EMR
Perform and maintain quality control records on all materials associated with the IVF lab and process
Insure that all laboratory procedures have properly consented prior to performing them
Communicate directly with physicians regarding daily IVF/ICSI and embryo development outcomes
Perform quality assurance and preventative maintenance
QUA Maintain, clean and disinfect of the IVF Lab and its equipment (especially the incubators)
Inform and work with nurses to coordinate daily procedure scheduling
Work with the Lab supervisor to maintain ART records for SART
Other duties as assigned
What You'll Bring:
The skills and education we need are:
Bachelors Degree in Biology or related field required
2+ years of experience, signed off on all embryology lab duties with minimal training required
Artisan and Matcher experience is a plus
Ability to work weekends and holidays on a rotating basis with other teammates
Ability to work independently
Exceptional written and verbal communication skills and attention to detail.
Ability to work as part of a team
Good research skills
Tech Savvy
Flexibility and willingness to learn at all times
Excellent multi-tasking abilities, communication and organizational skills
More important than the best skills, however, is the right person. Employees who embrace our mission, vision, and core values are highly successful.
What We Offer:
We are proud to provide a comprehensive and competitive benefits package tailored to support the needs of our team members across all employment types:
Full-Time Employees (30+ hours/week):
Medical, dental, and vision insurance, 401(k) with company match, tuition assistance, performance-based bonus opportunities, generous paid time off, and paid holidays
Part-Time Employees:
401(k) with company match and performance-based bonus opportunities
Per Diem Employees:
401(k) with company match
At Ovation Fertility, we promote and develop individual strengths in order to help staff grow personally and professionally. Our core values guide us daily to work hard and enjoy what we do. We're committed to growing our practice and are always looking to promote from within. This is an ideal time to join our team!
To learn more about our company and culture, visit here.
$85k-90k yearly 60d+ ago
Embryologist
FPG Services LLC
Scientist job in Colchester, VT
Job Description
Enjoy what you do while contributing to a company that makes a difference in people's lives. Ovation Fertility, one of the premier fertility centers in the United States, seeks experienced, compassionate, and dynamic team players who are committed to delivering exceptional patient care to join our growing practice. The work we do building families offers stimulation, challenge, and personal reward.
We have an immediate opening for an Embryologist to join our team in Colchester, Vermont. The schedule is Monday through Friday, 7:00 AM to 4:00 PM, with rotating weekends and holidays as needed. The pay range for this position is from $85,000 to $90,000 per year.
How You'll Contribute:
We always do whatever it takes, even if it isn't specifically our “job.” In general, the Embryologist is responsible for:
Undertake embryology laboratory procedures as directed
Attention to detail with an awareness and understanding of the sensitive and confidential nature of ART (Assisted Reproductive Technology) treatment
Comply with HIPAA privacy regulations
Training in latest technologies including, but not limited to: trophetoderm biopsy, oocyte vitrification, and complex micromanipulation skills
Demonstrate advanced knowledge of reproductive biology including the male and female reproductive system
Demonstrate excellent clinical skills and be able to lead and work in a team environment
Must be comfortable with the physical handling of oocytes, embryos and semen including hazardous specimens
Management of aseptic techniques
Must be competent in the correct assessment and grading of oocyte, embryo and sperm morphology
Perform clerical tasks diligently and follow established protocols and laboratory guidelines
Meticulous data entry into computer databases and software programs
Ability to maintain detailed and accurate patient logs and laboratory reports
Communicate detailed information to patients, staff and regulatory bodies
Desire to develop and coordinate clinical research projects
Develops and completes research projects which are publishable
Provides support for manuscript preparation and editing
Provides support for CAP inspection preparedness and inspections
Desire to obtain additional competency certification by the American Board of Bioanalysis
Clear, professional and timely communication with staff, physicians and patients
Participate in Continuing Technical Improvement exercises
Maintain technical proficiency in routine laboratory procedures
Assist in the preparation of routine and ad hoc analyses of data relating to performance of the laboratory and individual technologists and to specific research projects
Performs all procedures required for IVF cycles, including medium and dish preparation, egg retrieval, sperm preparation, fertilization check, embryo evaluation, cryopreservation and thawing, transfer, ICSI and assisted hatching. Experience with trophectoderm biopsy is preferred
Performs all andrology services, including preparation of semen samples for artificial inseminations and IVF, cryopreservation of sperm, and complete sperm analysis assessed by World Health Organization (WHO) standards
Performs laboratory quality control (QC), quality assessment (QA), and participates in quality improvement (QI) programs, record keeping and collection of data
Participates in research on oocytes cryopreservation, oocyte maturation, preimplantation genetic diagnosis and related research
Performs other duties as assigned, and in keeping with company policies, procedures and standards of patient care and initiatives toward continuous improvement at the individual and organizational level
Perform daily embryology (set-up's / egg retrievals / ICSI-IVF / fertilization -embryo development checks / embryo transfers / cryopreservation / testicular Bx preps-Cryo / embryo Bx for PGD) and reporting
Process semen specimens for artificial insemination/IVF-ICSI, hyaluran sperm binding assays and cryopreservation
Maintain, organize, scan and file patient results, making sure that all records are complete, including physician signatures, and accurate. Confirm results on the patient ART Summary sheets in EMR
Perform and maintain quality control records on all materials associated with the IVF lab and process
Insure that all laboratory procedures have properly consented prior to performing them
Communicate directly with physicians regarding daily IVF/ICSI and embryo development outcomes
Perform quality assurance and preventative maintenance
QUA Maintain, clean and disinfect of the IVF Lab and its equipment (especially the incubators)
Inform and work with nurses to coordinate daily procedure scheduling
Work with the Lab supervisor to maintain ART records for SART
Other duties as assigned
What You'll Bring:
The skills and education we need are:
Bachelors Degree in Biology or related field required
2+ years of experience, signed off on all embryology lab duties with minimal training required
Artisan and Matcher experience is a plus
Ability to work weekends and holidays on a rotating basis with other teammates
Ability to work independently
Exceptional written and verbal communication skills and attention to detail.
Ability to work as part of a team
Good research skills
Tech Savvy
Flexibility and willingness to learn at all times
Excellent multi-tasking abilities, communication and organizational skills
More important than the best skills, however, is the right person. Employees who embrace our mission, vision, and core values are highly successful.
What We Offer:
We are proud to provide a comprehensive and competitive benefits package tailored to support the needs of our team members across all employment types:
Full-Time Employees (30+ hours/week):
Medical, dental, and vision insurance, 401(k) with company match, tuition assistance, performance-based bonus opportunities, generous paid time off, and paid holidays
Part-Time Employees:
401(k) with company match and performance-based bonus opportunities
Per Diem Employees:
401(k) with company match
At Ovation Fertility, we promote and develop individual strengths in order to help staff grow personally and professionally. Our core values guide us daily to work hard and enjoy what we do. We're committed to growing our practice and are always looking to promote from within. This is an ideal time to join our team!
To learn more about our company and culture, visit here.
Job DescriptionDescription:
Stone is seeking an enthusiastic and dedicated environmental professional to join our Environmental Assessment and Remediation Services team. The successful applicant will work closely with our group of engaged professionals and a variety of partners, including project owners, responsible parties, municipalities, state and federal agencies, and other project stakeholders to lead the evaluation, design, and implementation of projects involving hazardous wastes in the environment. The candidate will serve as mentor for staff, provide senior technical support for a variety of projects at hazardous waste and brownfield redevelopment sites, and conduct business development activities. This position will report to the Director of Environmental Assessment and Remediation Services in Montpelier.
Work will involve a variety of analysis and design; preparation of engineering design calculations, drawings, and specifications; technical research and report writing; senior technical review of client deliverables, and successful identification and pursuit of project opportunities. The successful candidate will lead, direct, and review studies within their area of expertise; prepare proposal scopes of work and budgets; prepare work plans and reports, plans and specifications; prepare opinions of probable remedial and construction costs; and direct and mentor junior staff.
Requirements:
Required To be considered for this position, the following skills are required:
A strong interest in brownfield redevelopment and conducting environmental site investigation and remediation projects
A proven track record in business development
Proven experience in developing project plans, anticipating, and addressing project issues, managing and mentoring staff, leading meetings with clients, and directing the completion of technical reports
Excellent verbal and written communication skills
Capacity to successfully manage multiple tasks and objectives
Legally able to work in the United States (proper documentation required)
Preferred Skills/Experience
Team or group leadership
Strategic visioning
Demonstrated ability to work with Vermont state government agencies and contract vehicles desired with direct experience with the Vermont Investigation and Remediation of Contaminated Properties Rule
Experience Level and Education
A B.S. in Environmental or Civil Engineering or related field is required.
Twelve years of relevant experience in the technical skill areas described above are required.
An advanced degree can be used in substitution for two years of experience.
$77k-104k yearly est. 18d ago
Medical Technologist / Medical Laboratory Scientist / Clinical Laboratory Scientist
K.A. Recruiting
Scientist job in Fairfax, VT
Medical Technologist
Employment Type: Full-time (80 hours bi-weekly)
Schedule: 9:00pm - 7:00am, Monday-Thursday (weekends as needed)
Salary Range: $28.50 to $39.52 USD per hour + $5k Bonus
Responsibilities:
Perform clinical testing in all Laboratory sections
Process specimens following written procedures
Document actions in the Laboratory Information System
Conduct Quality Control procedures on tests, instruments, reagents, etc.
Calibrate instruments and comply with Safety and Infection Control procedures
Organize work independently to meet job requirements
Perform specimen collections, including blood draws
Prerequisites:
ASCP Board Certification (COP) as a Medical Laboratory Scientist or equivalent
Baccalaureate degree in Medical Technology or related science preferred
Non-traditional routes to skill level may be considered based on education and experience
Apply, or email your resume to Megan@ka-recruiting.com, or call/text 617-746-2768. Schedule a chat here.
Keywords: Burlington, Milton, Fairfax, Clinical Laboratory, Medical Laboratory, Vermont, and more
$28.5-39.5 hourly 4d ago
Applied Scientist 5
Oracle 4.6
Scientist job in Montpelier, VT
We are looking for a Principal Applied Scientist to join our Security Engineering organization and help define the future of security operations for Oracle's SaaS ecosystem. This role offers a rare and high-impact opportunity to shape how next-generation detection, response, and threat defense will work across one of the largest enterprise cloud environments in the world.
As a Principal IC, you will architect and develop advanced ML and behavioral models that enable a new class of adaptive, intelligence-informed security capabilities. You will work directly with massive, noisy, and adversarial telemetry; build models that must operate at extreme scale; and pioneer approaches that transform how our analysts, detections, and automated systems understand attacker behavior.
In this role you will:
+ Invent new ways to detect and disrupt attackers
+ Build machine learning foundations for an AI-driven SOC
+ Influence the architecture of detection pipelines for years to come
+ Operationalize research at petabyte scale
+ Raise the scientific bar across the security organization
You will work closely with Detection Engineering, Red Team, Threat Intelligence, and Data Engineering to identify meaningful signal, reduce noise, validate hypotheses, and translate research into production systems.
**Responsibilities**
**Research & Modeling**
+ Develop novel ML models for anomaly detection, identity analytics, time-series/sequence analysis, graph modeling, and pattern mining across noisy, high-volume telemetry.
+ Design experiments, baselines, evaluation metrics, and scientific methodologies for threat detection problems.
+ Build prototypes, run experiments, analyze results, and iterate quickly.
**Data & System Understanding**
+ Work with massive, sparse, high-cardinality datasets (1.2PB/day+) to extract signal from noise.
+ Create data-efficient modeling approaches (self-supervision, embedding models, sampling strategies, feature extraction).
+ Design inference strategies that work under tight cost, performance, and real-time constraints.
**Cross-Functional Technical Work**
Collaborate with Detection Engineering, Data Engineering, Red Team, and Threat Intelligence to define problem statements, understand attack patterns, and interpret telemetry.
+ Provide scientific insights and deep technical guidance to engineering partners building pipelines and detections.
+ Translate research prototypes into production-ready designs with engineering teams.
**Scientific Rigor**
+ Establish strong modeling baselines, validation methodologies, ablation studies, and well-defined success criteria.
+ Document findings, methodologies, and recommended approaches clearly and reproducibly.
+ Maintain awareness of current academic and industry research; apply relevant advances appropriately.
**Required Qualifications**
**Technical Expertise**
+ Deep knowledge of ML approaches relevant to security:
+ anomaly detection
+ statistical modeling
+ representation learning / embeddings
+ sequence models (RNNs, Transformers)
+ graph-based analysis
+ clustering and outlier detection
+ Strong understanding of:
+ adversarial ML challenges
+ noisy/weak/no-label environments
+ data imbalance and cost-sensitive modeling
+ model explainability and operational constraints
**Hands-On Skills**
+ Expert programming in Python, SQL; comfortable with Spark, Beam, Flink, or similar distributed data systems.
+ Ability to rapidly prototype models and experiment with large datasets using PyTorch, TensorFlow, JAX, or similar.
+ Experience building models that run in production, including monitoring, drift detection, and model evaluation.
**Experience**
+ PhD or Master's in Computer Science, Machine Learning, Applied Mathematics, or equivalent experience.
+ 10+ years of industry or research experience applying ML to real-world problems.
+ Experience with security telemetry, cloud logs, SIEM/EDR/XDR analytics, identity data, fraud detection, or similar adversarial domains strongly preferred.
+ Demonstrated impact through deployed models, patents, publications, or widely adopted research outputs.
Disclaimer:
**Certain US customer or client-facing roles may be required to comply with applicable requirements, such as immunization and occupational health mandates.**
**Range and benefit information provided in this posting are specific to the stated locations only**
US: Hiring Range in USD from: $139,400 to $291,800 per annum. May be eligible for bonus, equity, and compensation deferral.
Oracle maintains broad salary ranges for its roles in order to account for variations in knowledge, skills, experience, market conditions and locations, as well as reflect Oracle's differing products, industries and lines of business.
Candidates are typically placed into the range based on the preceding factors as well as internal peer equity.
Oracle US offers a comprehensive benefits package which includes the following:
1. Medical, dental, and vision insurance, including expert medical opinion
2. Short term disability and long term disability
3. Life insurance and AD&D
4. Supplemental life insurance (Employee/Spouse/Child)
5. Health care and dependent care Flexible Spending Accounts
6. Pre-tax commuter and parking benefits
7. 401(k) Savings and Investment Plan with company match
8. Paid time off: Flexible Vacation is provided to all eligible employees assigned to a salaried (non-overtime eligible) position. Accrued Vacation is provided to all other employees eligible for vacation benefits. For employees working at least 35 hours per week, the vacation accrual rate is 13 days annually for the first three years of employment and 18 days annually for subsequent years of employment. Vacation accrual is prorated for employees working between 20 and 34 hours per week. Employees working fewer than 20 hours per week are not eligible for vacation.
9. 11 paid holidays
10. Paid sick leave: 72 hours of paid sick leave upon date of hire. Refreshes each calendar year. Unused balance will carry over each year up to a maximum cap of 112 hours.
11. Paid parental leave
12. Adoption assistance
13. Employee Stock Purchase Plan
14. Financial planning and group legal
15. Voluntary benefits including auto, homeowner and pet insurance
The role will generally accept applications for at least three calendar days from the posting date or as long as the job remains posted.
Career Level - IC5
**About Us**
As a world leader in cloud solutions, Oracle uses tomorrow's technology to tackle today's challenges. We've partnered with industry-leaders in almost every sector-and continue to thrive after 40+ years of change by operating with integrity.
We know that true innovation starts when everyone is empowered to contribute. That's why we're committed to growing an inclusive workforce that promotes opportunities for all.
Oracle careers open the door to global opportunities where work-life balance flourishes. We offer competitive benefits based on parity and consistency and support our people with flexible medical, life insurance, and retirement options. We also encourage employees to give back to their communities through our volunteer programs.
We're committed to including people with disabilities at all stages of the employment process. If you require accessibility assistance or accommodation for a disability at any point, let us know by emailing accommodation-request_************* or by calling *************** in the United States.
Oracle is an Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability and protected veterans' status, or any other characteristic protected by law. Oracle will consider for employment qualified applicants with arrest and conviction records pursuant to applicable law.
$69k-96k yearly est. 34d ago
Data Scientist, Product Analytics
Meta 4.8
Scientist job in Montpelier, VT
As a Data Scientist at Meta, you will shape the future of people-facing and business-facing products we build across our entire family of applications (Facebook, Instagram, Messenger, WhatsApp, Oculus). By applying your technical skills, analytical mindset, and product intuition to one of the richest data sets in the world, you will help define the experiences we build for billions of people and hundreds of millions of businesses around the world. You will collaborate on a wide array of product and business problems with a wide-range of cross-functional partners across Product, Engineering, Research, Data Engineering, Marketing, Sales, Finance and others. You will use data and analysis to identify and solve product development's biggest challenges. You will influence product strategy and investment decisions with data, be focused on impact, and collaborate with other teams. By joining Meta, you will become part of a world-class analytics community dedicated to skill development and career growth in analytics and beyond.Product leadership: You will use data to shape product development, quantify new opportunities, identify upcoming challenges, and ensure the products we build bring value to people, businesses, and Meta. You will help your partner teams prioritize what to build, set goals, and understand their product's ecosystem.Analytics: You will guide teams using data and insights. You will focus on developing hypotheses and employ a varied toolkit of rigorous analytical approaches, different methodologies, frameworks, and technical approaches to test them.Communication and influence: You won't simply present data, but tell data-driven stories. You will convince and influence your partners using clear insights and recommendations. You will build credibility through structure and clarity, and be a trusted strategic partner.
**Required Skills:**
Data Scientist, Product Analytics Responsibilities:
1. Work with large and complex data sets to solve a wide array of challenging problems using different analytical and statistical approaches
2. Apply technical expertise with quantitative analysis, experimentation, data mining, and the presentation of data to develop strategies for our products that serve billions of people and hundreds of millions of businesses
3. Identify and measure success of product efforts through goal setting, forecasting, and monitoring of key product metrics to understand trends
4. Define, understand, and test opportunities and levers to improve the product, and drive roadmaps through your insights and recommendations
5. Partner with Product, Engineering, and cross-functional teams to inform, influence, support, and execute product strategy and investment decisions
**Minimum Qualifications:**
Minimum Qualifications:
6. Bachelor's degree in Computer Science, Computer Engineering, relevant technical field, or equivalent practical experience
7. Bachelor's degree in Mathematics, Statistics, a relevant technical field, or equivalent
8. 4+ years of work experience in analytics, data querying languages such as SQL, scripting languages such as Python, and/or statistical mathematical software such as R (minimum of 2 years with a Ph.D.)
9. 4+ years of experience solving analytical problems using quantitative approaches, understanding ecosystems, user behaviors & long-term product trends, and leading data-driven projects from definition to execution [including defining metrics, experiment, design, communicating actionable insights]
**Preferred Qualifications:**
Preferred Qualifications:
10. Master's or Ph.D. Degree in a quantitative field
**Public Compensation:**
$147,000/year to $208,000/year + bonus + equity + benefits
**Industry:** Internet
**Equal Opportunity:**
Meta is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state and local law. Meta participates in the E-Verify program in certain locations, as required by law. Please note that Meta may leverage artificial intelligence and machine learning technologies in connection with applications for employment.
Meta is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know at accommodations-ext@fb.com.
We are looking to fill a **Scientist III - (HPLC) Chromatography - Separations & Molecular Biology - Immunoassay Experience** position working as **a full-time employee of Parexel FSP on long-term assignment** onsite at one of our clients located in **Rahway, NJ.** This position offers full benefits, sick time, 401K, paid holidays, and paid time off. **This position does not offer any sponsorship.**
**Description**
Support of routine bioanalytical testing of samples from cell-line development, in-process, process development/characterization, forced degradation, release & stability, and pre-formulation. Other potential opportunities include method development/optimization, workflow optimization, and template development.
**Responsibilities**
+ Support of high-throughput, pre-formulation, pre-qualification, robustness, or admixture testing
+ Results processing and documentation by following appropriate methods / protocols / procedures
+ Sample management and monitoring of controlled temperature units.
+ Following all appropriate laboratory safety and hygiene procedures
**Qualifications**
+ BA/BS (3-5 yrs.) of relevant experience in analytical chemistry or biologics testing lab
+ MS (1-2 yrs.) of relevant experience in analytical chemistry or biologics testing lab
**Required Skills and Experience**
+ Must have separations experience for large molecules or plate-based assay experience.
+ Experience in analyzing biologics including monoclonal antibodies and/or other therapeutic proteins using at least one of the following techniques:
+ Liquid Chromatography (HPLC / UPLC)
+ Protein A Titer, Size Exclusion Chromatography (SEC), Ion Exchange Chromatography (IEX, AEX, CEX), Reverse Phase (RP), or Hydrophobic interaction chromatography (HIC)
+ Electrophoretic methods such as capillary electrophoresis sodium dodecyl sulfate (CE-SDS) and/or capillary isoelectric focusing (cIEF)
+ ELISA (HCP, proA) and binding potency assay
+ qPCR and basic molecular biology techniques (gel electrophoresis, etc.)
+ High-throughput liquid handling system, e.g., Tecan, Bravo, etc.
+ Basic instrumentation troubleshooting
+ **Ability and willingness to train in molecular biology and immunoassay testing**
+ **Familiarity with Microsoft Office Applications (Outlook, Excel, Word, PowerPoint, OneNote, Teams, etc.)**
**Desired Skills and Experience**
+ Familiarity with compendial testing such as UV 280, pH, and Physical Observations
+ **Ability to follow complicated scientific protocols / procedures**
+ Making accurate reagent preparations (dilutions / solutions / buffers / mobile phases)
+ Good documentation practices & utilization in electronic lab notebooks (ELN)
+ Analytical software such as Empower.
+ Knowledge of Laboratory Information Management Systems (LIMS)
+ Sample submission & sample management
+ Monitoring of controlled temperature units
+ Experience with BSL2 (Biosafety Level 2)
**About Parexel**
Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies.
For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement.
**Come join us!**
\#LI-DK1
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
is remote and can be based anywhere within the United States._ **At Cardinal Health, we're developing the innovative products and services that make healthcare safer and more productive. Join a growing, global company genuinely committed to making a difference for our customers and communities.**
The Sr. Scientist, Scientific Operations, Real-World Evidence will have responsibility to design, and/or conduct innovative Real-World Data (RWD) and Real-World Evidence (RWE) projects for biopharmaceutical manufacturers. This individual will have subject matter expert (SME) in healthcare research, with knowledge and understanding of biomarkers, treatment patterns, measurement of treatment efficacy, and tolerability through chart review, EMR, or administrative claims databases. The position requires strong verbal and written communications skills that are necessary to translate research findings into peer-reviewed abstracts and manuscripts.
**_Responsibilities_**
+ Provide research expertise on RWD/RWE studies in a principal-investigator level scientific role
+ Work in a role that is heavily client-facing and consultative, providing expert guidance on study objectives and methodology to life sciences partners
+ Support the generation of high-quality real-world research studies using chart review, administrative claims, and electronic medical record methods/data
+ Support the business development process by serving as an SME for healthcare research in terms of design, proposal development, protocol development, analysis, and reporting
+ Proactively address complex analytical issues with research analytics and research operations team members during the conduct of a study
+ Work in a fast-paced and accountable environment engaging on multiple projects with multiple manufacturers at the same time
+ Interact with internal and/or external leaders, including senior management
+ Guide members of multiple research teams into consensus in sensitive situations while maintaining positive relationships
+ Write and review research study concepts, protocols, statistical analysis plans, table shells, and reports (must have substantial writing and communication skills)
+ Determine appropriate research methods and data sources to deliver high-value and quality real-world research to pharmaceutical manufacturers
+ Communicate effectively and professionally with pharmaceutical RWE customers
+ Generate and review empirical abstracts and publications
+ Prepare and review responses to proposal requests for RWE/HEOR projects
+ Prepare RWE/HEOR data as background materials for discussion with pharmaceutical customers
+ Ability to provide excellent customer service when delivering work on projects
+ Develop expertise in RWE/HEOR through publications and presentations of scientific research
+ Collaborate with RWE team, as required, to compile evidence required to execute projects for pharmaceutical clients
**_Qualifications_**
+ Education: MA/MS or PhD in epidemiology, health services research, or similar field, highly preferred
+ Ability to travel a few times during the year for conferences and client meetings
+ 4+ years of relevant working experience (during employment and/or while obtaining advanced degree); 1 year in the pharmaceutical/medical industry within a pharmaceutical company or a pharmaceutical consulting company, highly preferred
+ Knowledge of RWE and HEOR and its application to specialty drugs within the US market
+ Leadership skills and problem-solving capability
+ Demonstrated success implementing projects, including engagement with key stakeholders, with high degree of autonomy
+ Excellent written and verbal communication skills, and presentation skills
+ Ability to travel domestically, as needed
**Anticipated salary range:** $123,400 - $141,000
**Bonus eligible:** Yes
**Benefits:** Cardinal Health offers a wide variety of benefits and programs to support health and well-being.
+ Medical, dental and vision coverage
+ Paid time off plan
+ Health savings account (HSA)
+ 401k savings plan
+ Access to wages before pay day with my FlexPay
+ Flexible spending accounts (FSAs)
+ Short- and long-term disability coverage
+ Work-Life resources
+ Paid parental leave
+ Healthy lifestyle programs
**Application window anticipated to close:** **01/19/26** *if interested in opportunity, please submit application as soon as possible.
_**The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity._
_Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply._
_Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal_ _Opportunity/Affirmative_ _Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law._
_To read and review this privacy notice click_ here (***************************************************************************************************************************
$123.4k-141k yearly 13d ago
CCB Lab Scientist II
State of Vermont 4.1
Scientist job in Colchester, VT
The Cannabis Control Board (CCB) is seeking motivated individuals to join our collaborative and dedicated team in the role of Laboratory Scientist II. The individuals in this role will join the CCB's state laboratory to conduct advanced chemical and microbiological analyses of cannabis samples. Working both independently and collaboratively under the direct supervision of the CCB Laboratory Director, they will serve as technical advisors and subject matter experts for CCB staff, laboratory management, and other stakeholders involved in cannabis testing.
This small, three-person team will play a hands-on role in establishing and developing laboratory processes and workflows as the new CCB lab becomes operational.
This position will have the shared responsibility for:
* Performing critical start-up activities such as sampling, testing, data analysis, and reporting, while managing multiple analytical projects.
* Preparing method development, optimization, and validation protocols and analytical technical reports
* Ensuring development and implementation of laboratory standard operating procedures.
This position is based in Colchester with access to CCB headquarter offices in Montpelier. The CCB is a small agency with a big mission, and this role demands a strong work ethic, occasional travel, and potential evening and weekend work to address emergent consumer safety issues as they arise.
Who May
$39k-52k yearly est. 18d ago
Medical Technologist / Medical Laboratory Scientist / Clinical Laboratory Scientist
K.A. Recruiting
Scientist job in Burlington, VT
Medical Technologist
Employment Type: Full-time (80 hours bi-weekly)
Schedule: 9:00pm - 7:00am, Monday-Thursday (weekends as needed)
Salary Range: $28.50 to $39.52 USD per hour + $5k Bonus
Responsibilities:
Perform clinical testing in all Laboratory sections
Process specimens following written procedures
Document actions in the Laboratory Information System
Conduct Quality Control procedures on tests, instruments, reagents, etc.
Calibrate instruments and comply with Safety and Infection Control procedures
Organize work independently to meet job requirements
Perform specimen collections, including blood draws
Prerequisites:
ASCP Board Certification (COP) as a Medical Laboratory Scientist or equivalent
Baccalaureate degree in Medical Technology or related science preferred
Non-traditional routes to skill level may be considered based on education and experience
Apply, or email your resume to Megan@ka-recruiting.com, or call/text 617-746-2768. Schedule a chat here.
Keywords: Burlington, Milton, Fairfax, Clinical Laboratory, Medical Laboratory, Vermont, and more