Research fellow jobs in Manchester, NH - 712 jobs

UII America, Inc., a subsidiary company of Shanghai United Imaging Intelligence Healthcare Co. Ltd. (UII), is building an organization of highly-motivated, talented and skillful AI experts and software developers to strengthen our R&D power and address the need of our innovative products in the USA market. United Imaging Intelligence (UII) is committed to providing AI solutions for medical devices, imaging, and diagnosis - to helping clients better understand and embrace AI. United Imaging Intelligence is led by two world-renown leaders in the AI industry. Together, they will lead UII in focusing on “empowerment” and “win-win.” UII empowers doctors and equipment in order for doctors and hospitals to win, for research institutions to win, and for third-party companies to win. UII America, Inc. is building a world-class research and development team in Boston, MA. We have immediate openings for Computer Vision and Robotics Research Interns with the following qualification requirements: · Ph.D./M.S student in Computer Science, Electrical Engineering, Robotics, Data Science, Biomedical Engineering, Statistics, Applied Mathematics, or other related fields; · Self-motivated and demonstrated problem solving and critical thinking skills; · Familiar with at least one mainstream deep learning toolkit, e.g., Pytorch, Tensorflow; · Familiar with Python, C++ and OpenCV; · Proven track record of publications in the top computer vision, machine learning and robotics venues such as CVPR, ICCV, ECCV, NeurIPS, ICML, ICLR, AAAI, ICRA, IROS, RSS, TPAMI, IJCV, T-RO, and IJRR is a plus; · Experience with 6D pose estimation, 3D visual perception, video understanding, efficient neural reconstruction, and embodied AI is a plus; · Excellent communication skills and team-work spirit. Main Responsibilities · Conduct top-tier research in the area of Computer Vision and Robotics in a collaborative team-working environment; · Working closely with full-time employees to come up with, implement, and verify research ideas; · Fast prototyping, and developing cutting edge AI assets for the company; · Contribute to intellectual properties, strong publications and transferring technologies into practical product solutions; · Be ambitious to change future Healthcare with innovations.

Site: Mass General Brigham Incorporated Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham. Job Summary The Research Compliance Associate is responsible for contributing to the overall success of the research compliance program at Mass General Brigham (MGB) as demonstrated by assisting with the development, oversight, and monitoring of research compliance functions through interpretation of MGB policy and local, state, and federal laws and regulations. The Research Compliance Associate should have a background in multiple research areas including, but not limited to, bench and laboratory research, animal research, human subjects research, international research activities, responsible conduct of research (RCR), research misconduct, research privacy, grants management, and controlled substances. The Research Compliance Associate will work under the direction of the Chief Research Compliance Officer and in collaboration with other departments within the research infrastructure. Qualifications Under the guidance of the Chief Research Compliance Officer, the Research Compliance Associate will have the following responsibilities: Assist with the development of an annual work plan based on risk assessment. Utilize metrics to measure program effectiveness. Assist with internal investigations and operational audits to assess risk of research related issues, identify potential research compliance vulnerabilities, and make recommendations to improve internal controls. Assist with education of the research community on research related topics to achieve compliance utilizing communication styles such as PowerPoint presentations, articles, website development, in-person training sessions, handouts, and infographics. Stay abreast of requirements and changes in the regulatory environment and assist with interpretation and distribution of emerging MGB policies as well as local, state, and federal laws and regulations as it relates to research compliance. Assist with evaluation of issues of non-compliance to include investigation, oversight, follow up, and resolution. Assist in the development and revision of written research policies, procedures, and guidelines. Assist in maintaining the research compliance webpage with relevant and up-to-date information in collaboration with the web development staff. Utilize tact and diplomacy to communicate, build rapport and foster strategic alliances within the research community. May represent Research Compliance at committee meetings. Contribute to MGB and the Office of Compliance initiatives to promote a positive work environment. Perform other related duties and responsibility as required. Education Bachelor's Degree required. Graduate degree in a healthcare field or law is preferred; related healthcare or legal experience considered in substitution Licenses and Credentials CHRC preferred Experience 3 years experience in project management in a complex organization required. 1-3 years experience in a research-related position, preferably in a research compliance role. Familiarity with current applicable local, state, and federal laws and regulations related to research activities. Knowledge, Skills and Abilities Proficient in using computer software applications such as Microsoft Excel, Word, PowerPoint, and Adobe. People Soft experience strongly preferred. Strong interpersonal and communication skills (oral and written), including public speaking to facilitate training sessions, and lead discussion groups. Ability to understand complex organizations; demonstrated political savvy. Strong project management skills Ability to work independently, with all levels, and within a strong team environment. Ability to manage multiple responsibilities, often under time pressures. Ability to function independently and effectively. Working Schedule Hybrid, depending on business needs. On average, onsite required 2 days per week. Additional Job Details (if applicable) Remote Type Hybrid Work Location 399 Revolution Drive Scheduled Weekly Hours 40 Employee Type Regular Work Shift Day (United States of America) Pay Range - / Grade 6 At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to your total compensation package. In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply, and our Talent Acquisition team will provide an overview of your potential compensation and benefits package. EEO Statement: Mass General Brigham Incorporated is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran's Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources at **************. Mass General Brigham Competency Framework At Mass General Brigham, our competency framework defines what effective leadership “looks like” by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.

Ballentine Partners is looking for an enthusiastic Research Associate to join our growing Investments team. This investment professional will assist in identifying opportunities and conducting due diligence across all major private market asset classes including private equity, private credit, and real assets, spanning both impact investment as well as non-impact investments. This role will be responsible for helping to manage the deal process from end to end. This individual will be a visible member of the team who will play a meaningful role in the research process, helping manage deals and providing support to the private portfolio. Responsibilities include: Working as part of the investment team to assist in private research and the evaluation of private investment opportunities Helping maintain database of managers and investments; reporting on status of managers in process currently and historically Helping identify and source investment opportunities in private funds and co-investments Helping maintain current partner relationships Evaluate macroeconomic, demographic, and societal trends to identify areas of investment Assisting in all steps of the investment process including due diligence, preparation, and presentation of investment committee materials Working with legal, accounting, and fund administration to execute transactions and manage the portfolio Promoting a culture of collaboration and willingness to work cross-functionally to add value across the investment platform Other duties as assigned The right candidate will be someone who has the following skills: Demonstrate curiosity and initiative in advancing knowledge A passion for investments that promote environmental and social good Proactively researches answers to questions before asking superiors Exhibit strong interpersonal and communication skills with internal teams and also external managers including presentation skills Assist with investment team and/or firm initiatives. Is comfortable working with senior stakeholders and sophisticated clients Is a highly analytical and fact-based thinker Has strong math and Excel modeling skills Will be adept at various software tools including manager databases and CRM systems, and can also help evaluate new software tools for inclusion in our processes Can take initiative and act proactively (i.e., anticipates problems, raises suggestions) Can work both independently and in a team structure with a diverse group of people Can take direction from multiple sources and prioritize a variety of tasks daily Can juggle and prioritize a variety of tasks daily Is highly organized with a very strong attention to detail Has strong communication skills, verbal and written Has excellent interpersonal & relationship skills including a positive and collegial attitude Has high professional standards, judgment, and discretion A Bachelor's Degree is required. Master's Degree and/or CFA designation (or progress toward) are a plus. At least 2 years of experience in a similar role is preferred. Private equity, venture capital, credit and/or real asset investing or manager due diligence experience a plus. Ballentine Partners offers a wide array of benefits completely paid for by the firm including dental, vision, short-term disability, long-term disability, and life insurance as well as cost sharing on medical insurance. We offer extensive time-off benefits including vacation time, unlimited personal sick time, paid family sick leave, paid parental leave, sabbaticals, community time off and so much more. We have a corporate matching program, and we support certifications and continuing education for our team members. Ballentine is a family-friendly and flexible work environment. Our culture is collaborative and built on supporting each other to grow not only the business but each other as well. For more information on our culture please view our Stakeholder Report and our Culture page. Ballentine Partners compensation is made up of a base salary and performance bonus. The salary range for this position is $95,000.00 - $120,000.00 and is commensurate with experience. Performance bonuses are based upon company and personal performance and are paid out annually. We will sponsor applicants for work visas. Ballentine Partners is an Equal Opportunity Employer and we are dedicated to providing an inclusive environment for all employees. All employment is based upon qualifications, merit, and business need. We encourage applications from those who share our commitment to promoting a diverse, welcoming, and inclusive community.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description: • Possess a sound knowledge of the chemical principles and concepts of preparing buffers and tissue culture media and aseptic techniques . • Use established procedures (SOP's) and based on experience, training, and education, interpret complex methodologies (Protocols) provided by scientists. • Utilize good laboratory practices while applying technical expertise to formulate buffers and tissue culture solutions. • Independently perform work in a controlled laboratory environment. May assist others in completing their work. • Document all work utilizing Media Prep Worksheet • Maintain appropriate records pertaining to solution preparation in a fashion that allows for easy data retrieval. • Assist the team with the documentation such as records, reports and worksheets. • Assist with the shipping logistics of the buffer and media solutions. • Perform other applicable duties as deemed appropriate by lab supervisor / manager. Qualifications Additional Skills: 2+ years experience with laboratory operations in a hospital or pharmaceutical setting. Additional Information For more information, please contact Sneha Shrivastava ************

FL87, Inc. is a privately held, early-stage biotechnology company developing a novel approach to gene therapy that can address currently untreatable diseases. It was founded by Flagship Pioneering, an innovation enterprise that conceives, creates, resources, and grows first-in-category life sciences companies. Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of which are pioneering novel and proprietary biological, industrial, and engineering approaches to solve major needs in human health and sustainability. These companies include Moderna (MRNA), Syros Pharmaceuticals (SYRS), Seres Therapeutics (NASDAQ:MCRB), Generate Biomedicines, Tessera Tx, Evelo Biosciences (EVLO), and Indigo Agriculture. The role We are seeking a motivated Research Associate / Senior Research Associate to support the development, preparation, and characterization of Lipid Nanoparticle (LNP) formulations. This role is highly hands-on and focused on formulating, screening, and analyzing LNPs to support discovery and development programs. The ideal candidate works well in a fast-paced, team-oriented environment and is eager to deepen their expertise in formulation science. Key responsibilities Prepare and formulate LNPs using established protocols and evolving methods Execute formulation experiments to support optimization and screening efforts Perform LNP characterization and analytics, including particle size, PDI, encapsulation efficiency, and stability testing Accurately document experimental procedures, results, and observations in laboratory records Analyze and summarize experimental data and communicate findings to project teams Collaborate closely with scientists across formulation, analytics, and biology functions Support routine laboratory operations, including reagent preparation, equipment upkeep, and inventory management Professional experience and qualifications BS or MS in Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering, or a related field Hands-on experience with LNP formulations or lipid-based delivery systems Familiarity with LNP analytical techniques (e.g., DLS, encapsulation assays, basic stability studies) Strong attention to detail and ability to follow experimental protocols Ability to work effectively as part of a team in a fast-paced environment Good written and verbal communication skills What We Offer Opportunity to work at the forefront of LNP formulation innovation Collaborative, science-driven culture with high impact research Competitive compensation and benefits package ABOUT FLAGSHIP PIONEERING Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture. Flagship has been recognized twice on FORTUNE Change the World list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company annual list of the World Most Innovative Companies. Learn more about Flagship *********************************************************************************************** At Flagship, we accept impossible missions to enable bigger leaps. Our core values guide us through uncertainty and toward lasting impact. We are an equal opportunity employer. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law. Recruitment & Staffing Agencies: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering's internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto. The salary range for this role is $65,000 - $93,500. Compensation for the role will depend on a number of factors, including a candidate's qualifications, skills, competencies, and experience. FL87 currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on FL87's good faith estimate as of the date of publication and may be modified in the future.

NO AGENCIES - PLEASE Please keep in mind - salary range / pay is factored on years of direct work experience and education . The Metabolomics/Lipidomics Research Associate will have experience in analytical chemistry, preferably in the space of metabolite and/or small molecule analysis using LC/MS and LC/MS/MS platforms. The Research Associate will perform targeted and nontargeted bioanalysis and assist with the development of novel methods to support the platform. ESSENTIAL DUTIES AND RESPONSIBILITIES: Responsible for the full spectrum of activities involved in metabolomics/lipidomics analysis as a member of the team, including the following: Conceptualize, perform, analyze, and report experiments. Perform mass spectrometry-based assays and studies focused on metabolite analysis of diverse samples from the biological matrices. Laboratory analytical instrumentation routine maintenance. Daily QA/QC, system suitability testing, method development, and validated SOP implementation Develop SOPs. Manage external collaborations. Other duties, as assigned. QUALIFICATIONS : Requires a B.S. (0-2 years of experience) or M.S. (with 0-1 years of experience) in analytical chemistry, biochemistry, or a related field, preferably in the analysis of small molecules by mass spectrometry. Broad understanding of metabolomics/lipidomics applications and biochemistry in the areas of systems biology, neurodegeneration, obesity, cardiovascular disease, and cancer is a plus. Experience with common sample preparation techniques is preferred but not required, including solid phase extraction (SPE), liquid-liquid extraction, and protein precipitation for biofluids, tissues, and cells. Familiarity with core chromatography and mass spectrometry concepts, including principles of reversed-phase LC and HILIC, high-resolution/accurate mass strategies, structural elucidation by MS/MS, and isotope dilution. Excellent communication and interpersonal skills combined with a proven track record of technical and organizational skills. Must be able to work in a team-oriented environment and demonstrate attention to detail and record-keeping. Must demonstrate fully professional level requiring independent work in metabolomics research and development. Knowledge of Microsoft Word, Excel, and PowerPoint required for preparation of reports for management. Ability to prepare manuscripts for presentation, publication in scientific journals, and regulatory requirements is preferred.

The individual will play a key role in the identification and functional characterization of lead molecules across diverse therapeutic areas and modalities. Success in this role will involve working directly with multiple individuals in the Discovery Assays group on a weekly basis and can involve interactions with individuals throughout the larger Discovery organization. • Execute established plate based biochemical and cell-based screening assays for biologics hit ID • Execute assays for functional characterization of leads • Expand range of technical skills to cover range of assays used in hit identification and lead characterization within the group • Document experimental details and scientific findings, strong attention to detail; use LIMS system for workflow and experimental tracking, actively participate in scientific meetings Qualifications Specialized knowledge and skills • Experience with ELISA development, FACS, Luminex, Octet, Alpha Screen, HTRF or MSD is desirable • Experience with cell culture • Familiarity with automation, electronic lab notebook or LIMS systems a plus • Excellent organizational, analytical and technical skills are required along with ability to work well within a team environment • Enthusiasm, willingness to learn, strong work ethic, broad scientific interests § Excellent interpersonal and communication skills along with a sense of urgency and ability to work on multiple projects simultaneously Non-PhD candidates with at least 2 years of relevant work experience Additional Information Please Connect with me at ************

The Research Contracts Specialist will draft, review, execute a high-volume of research agreements, and manage a limited number of consortiums. Works independently on DFCI template-based agreements and partners with manager and/or senior members on the Licensing and Contracts Teams on SRAs, non-exclusive reagent licenses. Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS, and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals. **Agreements/Transactions** + Uses institutional templates to guide negotiations and drafts creative language to address departures from templates. + Independently negotiates confidentiality agreement, material transfer agreements, data use agreements, multi-site and academic collaboration agreements and amendments to the foregoing. + Negotiates straightforward sponsored research agreements and non-exclusive research reagent licenses in partnership with manager and/or senior members on the Licensing and Contracts Teams. **PI Relationship Management/Communication** + Responds to inquiries from PIs and other parties, requiring manager input and participation on complex matters + Drafts complex written messages for final review + Coordinates and attends meetings with PIs and other parties, with contributing role in discussions + Manages consortiums and multi-party collaborations where DFCI is a non-lead member. + Familiar with institutional policies and practices. **KNOWLEDGE, SKILLS, AND ABILITIES REQUIRED:** + Comprehension of science and translation of medical innovation. + Working knowledge of federal, state and institutional policy relevant to duties and responsibilities + Detail-oriented + Excellent verbal and written communication skills required. Communicates proactively. + Excellent interpersonal skills + A self-starter with the ability to identify and recommend solutions. + Ability to work as a member of a team including taking work on from colleagues within knowledge base. + Ability to manage and prioritize numerous transactions and bring to closure in a timely manner. + Ability to represent DFCI and gain the confidence, trust and respect of clinicians, scientists, administrators, investors, external industry counterparts. + Ability to work in a highly matrixed and complex organization with multiple stakeholders. **MINIMUM JOB QUALIFICATIONS:** + A Bachelor's degree is required; JD is strongly preferred. + 1 year of contracts experience in an academic institution At Dana-Farber Cancer Institute, we work every day to create an innovative, caring, and inclusive environment where every patient, family, and staff member feels they belong. As relentless as we are in our mission to reduce the burden of cancer for all, we are committed to having faculty and staff who offer multifaceted experiences. Cancer knows no boundaries and when it comes to hiring the most dedicated and compassionate professionals, neither do we. If working in this kind of organization inspires you, we encourage you to apply. Dana-Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other characteristics protected by law. **EEO Poster** . Pay Transparency Statement The hiring range is based on market pay structures, with individual salaries determined by factors such as business needs, market conditions, internal equity, and based on the candidate's relevant experience, skills and qualifications. For union positions, the pay range is determined by the Collective Bargaining Agreement (CBA). $87,100.00 - $99,300.00

Your Impact at Lila We are seeking a Research Associate to join our Nucleic Acids team. This role will focus on supporting advanced DNA production and sequencing workflows, executing and continuously improving workflows and implementing process enhancements. The ideal candidate will have hands-on expertise in molecular biology techniques, a production-oriented mindset, and experience with automation technologies. This position will work closely with the others within the Life Sciences group to ensure seamless collaboration between DNA production and a variety of experimental workflows. What You'll Be Building Execute low, medium and high-throughput DNA production workflows, identify and address sources of variation to enhance efficiency, reliability, and scalability. Integrate and optimize custom automation technologies to streamline production processes. Collaborate with the members of the Nucleic Acids team and our Data Sciences and Machine Learning groups to onboard new workflows, resolve bottlenecks, and improve data systems. Write, implement, and maintain Standard Operating Procedures (SOPs) for both existing and new lab processes. Conduct data analysis and interpretation to monitor lab processes and drive process improvements. Provide operational leadership within the lab, coordinating activities and ensuring smooth execution of production workflows. What You'll Need to Succeed MSc in Molecular Biology, Biotechnology, or a related field with 1 years, or BSc with 3+ years, of high-throughput DNA production or related experience. Industry experience strongly preferred. Hands-on expertise in molecular biology techniques, including DNA cloning and sequencing. Experience with DNA library preparation for various downstream applications including ONT and Illumina sequencing and library construction. Experience working in high-throughput production environments with a focus on scalability and efficiency. Familiarity with integrated laboratory automation technologies and their application in DNA production workflows. Proven ability to identify and resolve process inefficiencies and implement phased improvements. Strong data analysis skills and ability to interpret workflow performance metrics. Excellent communication and collaboration skills, with a proven ability to work effectively across interdisciplinary teams. Bonus Points For Experience in designing and optimizing DNA assembly workflows for synthetic biology applications. Experience with assembling high diversity DNA libraries. Familiarity with digital systems and data pipelines used in high-throughput environments. Demonstrated ability to use electronic lab notebooks and write technical documentation, such as SOPs and validation reports. Knowledge of best practices for lab operations About Lila Lila Sciences is the world's first scientific superintelligence platform and autonomous lab for life, chemistry, and materials science. We are pioneering a new age of boundless discovery by building the capabilities to apply AI to every aspect of the scientific method. We are introducing scientific superintelligence to solve humankind's greatest challenges, enabling scientists to bring forth solutions in human health, climate, and sustainability at a pace and scale never experienced before. Learn more about this mission at *********** If this sounds like an environment you'd love to work in, even if you only have some of the experience listed below, we encourage you to apply. Compensation We expect the base salary for this role to fall between $72,000-$96,000 USD per year, along with bonus potential and generous early equity. The final offer will reflect your unique background, expertise, and impact. We're All In Lila Sciences is committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. Information you provide during your application process will be handled in accordance with our Candidate Privacy Policy. A Note to Agencies Lila Sciences does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Lila Sciences or its employees is strictly prohibited unless contacted directly by Lila Science's internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Lila Sciences, and Lila Sciences will not owe any referral or other fees with respect thereto.

At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where 'Health for all Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible'. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice. Computational Biologist, Principal Scientist - CVRI The Computational Biologist is responsible for the evaluation of therapeutic hypotheses via integration and quantitative analyses of internal & external multi-omics data sources (DNA, RNA, proteomics, metabolomics, imaging, etc) for CardioVascular, renal and immunology Therapeutic Areas. Significant contributions to innovative research and development projects or collaborations, such as: identifying new targets with multi-omics evidence; assessing the link between targets and disease biology; proposing pharmacodynamic, efficacy or selection biomarkers; evaluating biomarker hypotheses from clinical trial specimens; assessing novel technologies; supporting therapeutic lifecycle management. Adopts and contributes to Best Practices for novel technologies, quantitative analyses, visualizations, and biological insight generation from multi-omics data sources. YOUR TASKS AND RESPONSIBILITIES The primary responsibilities of the Computational Biologist are to: Evaluate and contextualize the molecular evidence supporting a therapeutic hypothesis with relevant internal and external multi-omics data (DNA, RNA, proteomics, metabolomics, imaging, etc); Contribute to Project Team scientific strategy and prosecution of critical path objectives, such as the identification of novel targets, biomarkers, or patient selection hypotheses. These contributions use state-of-the art computational biology methods to analyze large and complex human data sets; Deliver biological insights on therapeutic assets and disease biology understanding to Project Teams, who apply these insights towards stage-gate decisions, portfolio prioritization, and/or submissions to Health Authorities; Educate Project Teams on innovations in disease understanding in the CardioVascular, renal and immunology Therapeutic Areas; Develop, evaluate, implement, and apply Best Practices for the execution and validity of quantitative analyses, integration, visualizations, and interpretation of multi-omics data. Demonstrate a growth mindset towards updating Best Practices with the emergence of new experimental or computational technologies; Build cross-functional relationships to collaboratively partner across Pharma R&D and effectively network within disease understanding and data science communities of experts. WHO YOU ARE Bayer seeks an incumbent who possesses the following: Required Qualifications: PhD degree with post-graduation experience in Sciences (Bioinformatics, Computational Biology, Biology, Chemistry, Genetics, Computer Science, Informatics, or other related quantitative discipline) with very strong computational focus; Demonstrated experience in statistical analysis of DNA-seq, RNA-seq, proteomics, single-cell, or imaging datasets with proficiency in a programming environment (such as R or Python); Demonstrated hands-on experience in analysis of large scale proteomics, metabolomics datasets; Demonstrated peer-reviewed publications in computational biology; Expert level of proficiency to choose fit-for-purpose quantitative analyses; Strong analytical thinking and scientific rigor; Strong communication competencies to include presentations and delivery of complex quantitative analyses in a clear, concise, and actionable manner to broad audiences and key stakeholders across multiple functions or to external partners; Learning agility, highly self-motivated, with an aspiration of continuous improvement of oneself and others; Evidence of providing tactical and strategic guidance to the pharma portfolio or data science ecosystem; Demonstrated ability to propose, catalyze, and implement the development of interdisciplinary, systematic solutions that create business value; Capability to present even very complex issues clearly and convincingly to project teams or decision bodies. Good communication skills. Can manage a high degree of complexity; Demonstrates advanced business acumen, people and project leadership competencies, and technical expertise. Preferred Qualifications: 5+ years of post-graduation experience in Sciences (Bioinformatics, Computational Biology, Biology, Chemistry, Genetics, Computer Science, Informatics, or other related quantitative discipline) with very strong computational focus; 3+ years industry experience in drug development or biotech role with clear understanding of applying multi-omics data analyses to advance a portfolio of drug discovery or clinical development projects. Employees can expect to be paid a salary between $124,864.80 - $187,297.20. Additional compensation may include a bonus or commission (if relevant). Additional benefits include healthcare, vision, dental, retirement, PTO, sick leave, etc. This salary range is merely an estimate and may vary based on an applicant's location, market data/ranges, skills, prior relevant experience, certain degrees and certifications, and other relevant factors. This posting will be available for application until at least 1/29/2026. YOUR APPLICATION Bayer offers a wide variety of competitive compensation and benefits programs. If you meet the requirements of this unique opportunity, and want to impact our mission Science for a better life, we encourage you to apply now. Be part of something bigger. Be you. Be Bayer. To all recruitment agencies: Bayer does not accept unsolicited third party resumes. Bayer is an Equal Opportunity Employer/Disabled/Veterans Bayer is committed to providing access and reasonable accommodations in its application process for individuals with disabilities and encourages applicants with disabilities to request any needed accommodation(s) using the contact information below. Bayer is an E-Verify Employer. Location: United States : Massachusetts : Cambridge Division: Pharmaceuticals Reference Code: 855418 Contact Us Email: hrop_*************

STRM.BIO (pronounced “storm bio”) is a VC-backed biotech startup building a new kind of gene therapy delivery platform based on naturally occurring extracellular vesicles (EVs). We're leveraging the unique biology of EVs to unlock targeted, scalable, and low-immunogenicity genetic medicines that target the bone marrow. We're a small, fast-moving team based at The Engine in Cambridge, MA. We believe in simplicity, integrity, and keeping people at the center of everything we do. We're here to do great science and build a company we're proud of. THE OPPORTUNITY We're looking for Research Associates to help grow our research engine. You'll work shoulder-to-shoulder with technical leadership and a team of Scientists to support key programs and facilitate external collaborations. This is a hands-on, highly cross-functional role ideal for someone who's ready to dive in and execute in equal measure. This is a full-time, on-site role. WHAT YOU'LL DO (Key Responsibilities) Support the Research Team in efforts across multiple collaborative research programs Contribute to R&D efforts to meet project milestones, maintaining the standards of scientific rigor and adhering to ethical standards Maintain standards consistent with company culture and values Work closely with team members to maintain project development, implementation and troubleshooting of experiments Generate, analyze, and share experimental results and ensure that all protocols, reagents, data, and analyses are documented following data integrity principles and prepared and made available in a timely manner Attend team meetings to discuss results, future plans and experiments, with a keenness to help achieve company milestones Maintain comprehensive and up-to-date knowledge of molecular and cellular biology techniques Perform other duties as assigned, including all those associated with facilitating the smooth operation of a wet lab environment Maintain accurate records in electronic lab notebooks (ELNs) and contribute to documentation for internal reports and regulatory filings Attend regular EHS meetings and maintain accurate biologic and chemical records WHAT YOU BRING (Required Qualifications) B.S. or M.S. in biology, immunology, bioengineering, or related field Some prior industry experience is strongly preferred Familiarity with gene-editing technologies (e.g., CRISPR, TALEN, ZFNs) and delivery platforms (e.g., viral vectors, LNPs, exosomes) Previous involvement in in vivo studies or willingness to learn animal handling and vivarium protocols Strong organizational and communication skills, with comfort operating in interdisciplinary project teams Prior experience with CRO collaboration or CMC workflows is a bonus KEY POSITION DETAILS 100% on-site in Cambridge, MA Full time with competitive compensation The salary range for this position is $70,000 to $90,000 USD annually. This salary range is an estimate, and the actual salary may vary based on various factors, including, without limitation, individual education, experience, tenure, skills, and abilities, as well as internal equity and alignment with market data, including potential adjustments for geographic location.

STRM.BIO (pronounced “storm bio”) is a VC-backed biotech startup building a new kind of gene therapy delivery platform based on naturally occurring extracellular vesicles (EVs). We're leveraging the unique biology of EVs to unlock targeted, scalable, and low-immunogenicity genetic medicines that target the bone marrow. We're a small, fast-moving team based at The Engine in Cambridge, MA. We believe in simplicity, integrity, and keeping people at the center of everything we do. We're here to do great science and build a company we're proud of. THE OPPORTUNITY We're looking for Research Associates to help grow our research engine. You'll work shoulder-to-shoulder with technical leadership and a team of Scientists to support key programs and facilitate external collaborations. This is a hands-on, highly cross-functional role ideal for someone who's ready to dive in and execute in equal measure. This is a full-time, on-site role. WHAT YOU'LL DO (Key Responsibilities) Support the Research Team in efforts across multiple collaborative research programs Contribute to R&D efforts to meet project milestones, maintaining the standards of scientific rigor and adhering to ethical standards Maintain standards consistent with company culture and values Work closely with team members to maintain project development, implementation and troubleshooting of experiments Generate, analyze, and share experimental results and ensure that all protocols, reagents, data, and analyses are documented following data integrity principles and prepared and made available in a timely manner Attend team meetings to discuss results, future plans and experiments, with a keenness to help achieve company milestones Maintain comprehensive and up-to-date knowledge of molecular and cellular biology techniques Perform other duties as assigned, including all those associated with facilitating the smooth operation of a wet lab environment Maintain accurate records in electronic lab notebooks (ELNs) and contribute to documentation for internal reports and regulatory filings Attend regular EHS meetings and maintain accurate biologic and chemical records WHAT YOU BRING (Required Qualifications) B.S. or M.S. in biology, immunology, bioengineering, or related field Some prior industry experience is strongly preferred Familiarity with gene-editing technologies (e.g., CRISPR, TALEN, ZFNs) and delivery platforms (e.g., viral vectors, LNPs, exosomes) Previous involvement in in vivo studies or willingness to learn animal handling and vivarium protocols Strong organizational and communication skills, with comfort operating in interdisciplinary project teams Prior experience with CRO collaboration or CMC workflows is a bonus KEY POSITION DETAILS 100% on-site in Cambridge, MA Full time with competitive compensation The salary range for this position is $70,000 to $90,000 USD annually. This salary range is an estimate, and the actual salary may vary based on various factors, including, without limitation, individual education, experience, tenure, skills, and abilities, as well as internal equity and alignment with market data, including potential adjustments for geographic location. Powered by JazzHR gv0rAcypFW

Wave Life Sciences is a biotechnology company focused on unlocking the broad potential of RNA medicines to transform human health. Our RNA medicines platform, PRISM, combines multiple modalities, chemistry innovation and deep insights in human genetics to deliver scientific breakthroughs that treat both rare and prevalent disorders. Our toolkit of RNA-targeting modalities includes editing, splicing, RNA interference and antisense silencing, providing us with unmatched capabilities for designing and sustainably delivering candidates that optimally address disease biology. Our diversified pipeline includes clinical programs in Duchenne muscular dystrophy, Alpha-1 antitrypsin deficiency and Huntington's disease, as well as a clinical program in obesity and a preclinical program in NASH/MASH. Driven by the calling to “Reimagine Possible”, we are leading the charge toward a world in which human potential is no longer hindered by the burden of disease. Description: Wave Life Sciences is seeking a highly motivated Research Associate in oligonucleotide chemistry to join its team in Lexington, Massachusetts. This is an ideal opportunity for an individual who is interested in learning cutting edge technologies and who thrives in a team-oriented, fast-paced, cross-disciplinary biotech environment. The candidate will take an active role in high-throughput oligonucleotide synthesis, purification and analytical characterization for discovery-related activities. This is an onsite position located in our Lexington office. Experience: B.S. in Chemistry or related discipline with 2-4 years of experience or M.S. with 0-2 years of experience Responsibilities: Play a key role in stereopure oligonucleotide synthesis and purification in a 96-well plate format for multiple projects/targets Characterization of oligonucleotides by analytical techniques i.e. UV, pH, UPLC and LC-MS Operate and maintain lab equipment such as MerMade synthesizers, ÄKTA purifiers, UPLC, LC-MS, Nanodrop, speed vac, lyophilizers, etc. Maintain detailed written and electronic records of experimental protocols and data in accordance with company policy Presentation of results in written and oral format within a multidisciplinary team Establish and maintain excellent working relationships within the team and with collaborative partners throughout the company Key Skills: Familiarity with solid-phase synthesis would be favorable Experience with HPLC purification preferred Understanding of analytical techniques such as UPLC and LC-MS preferred Demonstrable organizational and time management skills while handling multiple projects Ability to be highly productive and innovative in a fast-paced work environment Pay Range External Disclosure Statement The annual base salary for this position is $72,000 - $92,000. The range provided is based on what we believe is a reasonable estimate for the annual base salary pay range for this position at the time of posting. Actual annual base salary will vary based on several factors including, but not limited to, relevant skills, experience, qualifications, position criticality, and internal equity. This position is eligible for a discretionary annual bonus and discretionary stock-based long-term incentives. In addition to compensation, Wave offers a comprehensive and competitive range of benefits designed to support our employees' and their families physical and financial health and overall well-being. These include, but are not limited to, company-sponsored medical, dental, vision, life, long and short-term disability insurances, generous paid time off (including a week-long company shutdown in the Summer and the Winter), 401K participation with matching contributions, and Employee Stock Purchase Program. Wave Life Sciences provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, Wave Life Sciences complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. Wave Life Sciences expressly prohibits any form of workplace harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. Improper interference with the ability of Wave Life Sciences' employees to perform their job duties may result in discipline up to and including discharge. We value our relationships with professional recruitment firms. To protect the interests of all parties, and given the large volume of inquiries received from third-party placement agencies, we are not able to respond to all agency inquiries. We do not accept unsolicited resumes from any source other than directly from candidates for current or future positions. Submission of unsolicited resumes in advance of a signed agreement between our company and a placement agency does not create an implied obligation and, if an unsolicited candidate represented by a placement agency is hired, we are not obligated to pay a fee. Only approved recruitment firms will be allowed to provide services to Wave Life Sciences, USA.

Biocytogen is a comprehensive research and discovery service provider for biotech and pharmaceutical industry and academic institutions. Its service platform integrates preclinical studies with innovative animal models, CRISPR-based gene editing, and animal supplies, with the current focus on immuno-oncology and oncology. We are looking for a highly motivated research associate with the ability to work both independently and in a collaborative manner. Biocytogen is a fast-growing company and has an abundance of opportunities available for you to grow your career. Biocytogen is committed to nurturing junior scientists to progress within our organization, providing a supportive environment for career advancement. This opportunity is ideal for individuals who can recognize and seize learning opportunities. Job Responsibilities: ● Perform preclinical pharmacology studies in rodents. Tasks include drug administration via multiple routes (IV, IP, SC, PO etc), blood and tissue collection, and tumor volume measurement. Experience with small animal surgery is a plus. ● Communicate and coordinate with other scientists on a project team to draft, finalize, and implement study protocols. Follow protocols and independently execute tasks. ● Collect and record data. Prepare summaries of experimental procedures and results and present data in team meetings. ● Develop, perform, interpret, and troubleshoot a broad range of in vitro assays including immune cell profiling, cytokine profiling, functional assays using primary cells, as well as cytotoxicity/apoptosis assays using primary and/or cultured cells. ● Innovate and expand our assay portfolio by identifying, evaluating, and implementing new assay technologies through literature research, academic collaborations, and adaptation from other groups within the company. Requirements ● Bachelor's or Master's degree with 1-3 years of academic or industry research experience. Demonstrated experience in small animal handling and pharmacology is highly preferred. ● Experience with small animal handling, drug administration, and blood and tissue collection is preferred. ● Experience in cell biology, biochemistry, and/or molecular biology, in particular assay development and execution, is required. This includes cell-based assays, tissue culture, biochemical assay technologies, and protein and RNA expression analysis. ● Experience with cell culture and in vitro assays is desirable. ● Experience in primary immune cell-based assays is strongly preferred. ● Experience in flow cytometry (FACS) analysis is preferred. ● Demonstrate ability for quality execution, attention to detail, and proficiency in multi-tasking in a fast-paced environment. ● Collaborative team player. Be flexible and prioritize tasks based on team and company goals. ● Communicate effectively at all levels, within teams, with internal and external collaborators. ● Strong organizational skills. Maintain research data and records with the highest integrity. ● Ability to multitask in a fast-paced environment. Benefits Medical Insurance Dental Insurance Vision Insurance Health Reimbursement Accounts Life and AD&D Insurance Short & Long Term Disability Insurance 401K with Company Match Paid Time Off Paid Sick Days & Holidays BIOCYTOGEN is an Equal Opportunity Employer. Employment opportunities at BIOCYTOGEN BOSTON CORP are based upon one's qualifications and capabilities to perform the essential functions of a particular job. All employment opportunities are provided without regard to race, color religion, sex, national origin, ancestry, age, sexual orientation, gender identity and expression, veteran status, military status, disability, mental illness, genetic information, or any other characteristic protected by law. This Equal Employment Opportunity policy governs all aspects of employment, including, but not limited to, recruitment, hiring, selection, job assignment, promotions, transfers, compensation, discipline, termination, layoff, access to benefits and training, and all other conditions and privileges of employment.

Job Description Work closely with Scientists to evaluate antibodies, proteins, small molecules, and drugs by in vitro cell-based assays including cytotoxicity assays, flow cytometry, functional assays, and molecular biology assays, including ELISA, WB, ect. Job will involve maintaining cell lines, setting up and developing in vitro assays, working closely with in vivo team to supply cells and then receive ex vivo samples and analyzing assays with harvested blood serum/tissue, and maintaining a lab notebook. Powered by JazzHR YmFHsmtNfV

Torus Therapeutics is a new biotech company founded by Atlas Venture that is developing transformative gene therapies for severe genetic and rare diseases. Torus Therapeutics uses a unique and proprietary platform that is differentiated from current viral and mRNA gene therapy approaches. Join Torus' dynamic and growing team as we build the product platform to bring much-needed therapies to patients. Job Description Torus seeks a highly-motivated research associate contractor to support daily operations in the molecular biology laboratory. The successful candidate would report directly to the Senior Scientist, Platform Development and will assist in the development of Torus's overall platform technology. Primary Responsibilities include: Perform experiments supporting novel gene therapy platform Develop and execute analytical methods for the evaluation of novel constructs Execute analytical studies to evaluate gene expression Design, develop and organize novel libraries of gene therapeutics Conduct small-scale purifications to support process development Assist in the generation and review of protocols and reports Prepare, evaluate, and present data internally to cross functional teams Qualifications B.S. in Biology, Biochemistry, Molecular Biology or related discipline 1-3 years of relevant lab experience is ideal Experienced with molecular biology techniques (Western blot, qPCR, cloning) Primary laboratory presence (≥50%) required Strong communication, interpersonal and organizational skills Must have excellent attention to details Strong collaboration and team-working skills Candidate must be able to work independently and organize activities Additional Information We look forward to receiving your application! All your information will be kept confidential according to EEO guidelines. Please no agencies at this time.

Synapse Energy Economics is a research and consulting firm specializing in energy, economic, and environmental topics with a focus on resource and policy issues in the electric industry. Our work supports a broad range of public-interest clients, including consumer advocates, environmental organizations, regulatory commissions, and state and federal agencies. We place great value on the culture of our office: we are an energetic, forward-thinking, collaborative and supportive group of professionals, with a passion for public interest and sustainability. We are located in Central Square in Cambridge, Massachusetts. Please visit our website at ********************** for more information and examples of our work. Synapse Energy Economics is seeking ambitious, articulate and creative researchers and analysts with exceptional quantitative and writing skills. The ideal candidate is eager to learn about Synapse's wide range of expertise, and has a strong interest in analyzing large data sets to uncover key insights about the electric industry. We are seeking applications for both an Associate position and an entry-level Research Associate position. Successful applicants will work with Synapse staff members on the following types of projects, depending on client needs and the applicant's interests, skills, and experience: Simulating electric power system operations to project prices and environmental impacts Evaluating the cost-effectiveness of emissions control technologies and compliance scenarios Quantifying economic and environmental impacts of proposed generation, transmission, alternative energy, and energy efficiency projects Analyzing state, federal, and regional policies to reduce greenhouse gas emissions Applying models Developing and supporting open-source tools Clean Power Plan compliance planning Electricity ratemaking to support public benefits Qualifications Bachelor's degree in economics, statistics, engineering, environmental science, public policy, or related field. Candidates for the Associate position should also have 3 to 5 years of experience, or a master's degree in a similarly relevant field. We strongly prefer a focus on energy. Strong to exceptional quantitative, communication, and analytical skills, including: strong spreadsheet analysis skills and the ability to learn and master new analytical tools and capabilities; and excellent writing skills. While not required, computer programming skills, statistical analysis capabilities, and experience with data extraction tools are a plus. A demonstrated commitment to public interest issues, such as sustainability, environmental justice, and consumer protection. We Offer Opportunities to work with established experts on cutting-edge policy on behalf of public entities dedicated to consumer welfare and the environment; A friendly, open, and flexible work environment; and Competitive salary and benefits. To Apply Please email a cover letter and resume to Evelina Gulbinas at ***********************. In your cover letter, please describe how you meet each of the qualifications listed in the job description. You may also apply using the link below.

Scismic is supporting the growth of a Cambridge, MA biotech startup that is pioneering mRNA-modulating therapies to cure a broad range of genetic diseases. The company is exploring the use of its novel platforms in neurological disorders, heart disease, and muscular dystrophies. Position summary: As an expert scientist in cellular neurobiology, you will be responsible for establishing cellular assays to demonstrate in vitro proof of concept for company tRNA therapeutic leads and characterize the cellular activity and downstream disease-relevant biology to help prioritize candidates for in vivo studies. Key responsibilities for this position include: Establish in vitro disease models in relevant cell types including primary neurons and glia isolated from transgenic animal models and patient-derived iPSC lines. Design, troubleshoot, and execute cell-based assays in human and rodent cell lines to characterize the efficacy and safety of company's novel tRNA therapeutic leads. Understand mechanism of action of lead candidates and establish assays and endpoints relevant to downstream target and disease biology. Conduct literature searches; communicate understanding in internal forums and with external collaborators and partners. Minimum qualifications: A BS/MS in Neurobiology, Molecular/Cellular Biology, physiology, or a related discipline. Extensive hands-on experience with a variety of molecular, cellular and/or physiological techniques (isolating rodent neurons and establishing primary neuronal cultures, neurite outgrowth, qPCR, western blotting, microscopy, calcium imaging, synaptic imaging, multi-electrode arrays, human IPS/ES cell culture, etc). Prior experience using AAV/lentivirus in primary or iPSC-derived neurons is highly desirable. Ability to master new concepts and technologies quickly and run experiments independently. Scientifically rigorous, highly organized, with excellent oral and written communication skills. Ability to work independently as well as collaborate with colleagues and effectively prioritize and manage multiple tasks in a fluid, fast-paced work environment Title commensurate with level of experience. We are accepting applications to build a pipeline of potential candidates for future opportunities. If your qualifications align with our requirements, we will contact you once the hiring process begins. Thank you for your interest in this role.

Job DescriptionParallel Squared Technology Institute (PTI) is a non-profit research institute aiming to catalyze a leap in protein analysis technology and use it to explore new biological frontiers. PTI supports open research and educational opportunities supporting rapid career development for scientists, engineers, and mathematicians. Why? Protein dysfunctions directly cause many diseases, such as Alzheimer's disease. Yet, proteins remain understudied because of technological hurdles. How? To resolve these limitations, PTI will develop mass tags enabling a new framework for multiplexed protein analysis by mass spectrometry towards achieving 100-fold increase in throughput. Scientists at and collaborating with the institute will use these gains to directly investigate disease mechanisms and resolve problems that have proven intractable for decades. Our proof of principle technology and strategies are outlined at: parallelsq.org. PTI's new approach requires synergy between a diverse team of chemists, machine learning engineers, biologists, and mass spectrometrists. Alzheimer's disease and aging will be among the first focuses of this technology-driven research organization. New career opportunities Members of PTI will be supported with industry-level resources to lead research projects and disseminate their discoveries and innovations to the broader biomedical community through frequent publications, presentations, and submissions to public data portals. Summary of PositionWe are looking for either a Research Associate or Senior Research Associate who is interested in mass spectrometry. This person will be working on maintaining MS instruments for running multitudes of samples for a variety of projects in addition to other responsibilities. In order to be seriously considered for this position, we require a cover letter as part of the candidate's application.Responsibilities You will learn how to set up, operate and maintain mass spectrometers from multiple major vendors. Protein sample preparation. Inventory management for reagents and samples. Analyze experimental data and interpret results for internal and public presentation. Preparation of lab reagents and media. Required Qualifications Bachelor's degree in Chemistry, Biology, or related field. Advanced degrees or >2 years of experience will be considered for Senior RA position. Basic proficiency with biochemistry techniques or chemistry techniques. Demonstrated enthusiasm and interest in analytical chemistry. High level of initiative and flexibility, excellent communication and teamwork skills. Attention to detail. Good time management. Preferred Qualifications Familiarity with analytical techniques, mass spectrometry preferred. Familiarity with liquid chromatography. Protein and peptide sample preparation and purification methods. Who Will Love This Job You are passionate about science and technology and are eager to work in a team environment. You love learning new techniques, new technologies, and new concepts. You want an environment that will support your future plans as a scientist or engineer. You are committed to open science ideas and want to see your work disseminated broadly. We Offer An opportunity to change the world and work with some of the smartest and the most talented experts from different fields. Excellent medical, dental, and vision insurance with many $0 premium options for you and your family with several national and regional providers. Most employees have more than 20 plan options to choose from. Company-paid group life, AD&D, long- and short-term disability insurance 15 days PTO + 10 sick days per year 18 company holidays + your birthday off $5,000 per year educational reimbursement Up to 16 weeks paid parental leave Industry competitive salary We aim to help fill a structural gap in today's R&D system. We enable fundamental research that requires unusual levels of scale and coordination yet is not rapidly monetizable by industry. We're bringing together top talent from academia, industry, and startups to build a new model for innovative R&D. As an incubator within the Schmidt Futures Network, we identify high-impact scientific or technical research and development opportunities, ultimately defining and launching these projects as Focused Research Organizations. We are an Equal Employment Opportunity employer that proudly pursues and hires a diverse workforce. We do not make hiring or employment decisions on the basis of race, color, religion or religious belief, ethnic or national origin, nationality, sex, gender, gender-identity, sexual orientation, disability, age, military or veteran status, or any other characteristic protected by applicable local, state, or federal law or company policy. We strive for a healthy and safe workplace and strictly prohibit harassment of any kind. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.