401 Results for

Clinical Scientist Jobs in Princeton, NJ

Jobs

Basking Ridge, NJ30+ days ago

$242,700–$404,500 Per Year
Full-time

p style="margin:0in;line-height:normal;font-size:12pt;font-family:'aptos' , sans-serif">Download Our Benefits Summary PDF. Lead scientist team to collaborate with safety physicians, regulatory affairs, clinical development, other functions and external partners to deliver high-quality safety assessments, regulatory submissions, aggregate reports, and responses to health authority queries.

New!

Princeton, NJ1 day ago

$23–$27 Per Hour

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America.

Perform functionality testing on devices and support group scientists with device assembly and testing.

Basking Ridge, NJ30+ days ago

$280,350–$467,250 Per Year
Full-time

p style="margin:0in;line-height:normal;font-size:12pt;font-family:'aptos' , sans-serif">Download Our Benefits Summary PDF. Specific responsibilities will vary depending on the stage of development of assigned projects (i.e., Phase I through commercialization).

Job Description.

Warren, NJ30+ days ago

Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to the primary work location and the chosen candidate’s relevant skills, experience, and education.

Designs and optimizes formulations to achieve drug product properties for controlled delivery of drugs (i.e. oral, transmucosal, and topical) .

NJ30+ days ago

$133,579–$199,501 Per Year

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Author (and/or work with external medical writers to develop) clinical documents including but not limited to clinical protocols/amendments, briefing documents, IND annual reports, Investigators Brochures, clinical study reports, scientific presentations including abstracts, posters and manuscripts.

Ensure clinical data collection proceeds in a manner consistent with strategic objectives and regulatory requirements for reporting (i.e., collaborate with statisticians to produce statistical analysis plans and data displays; provide input to CRF design and data management processes; perform periodic review of clinical data).

New!

Rahway, NJ3 days ago

$117,000–$184,200 Per Year

p>Required Skills:

Clinical Data, Clinical Protocol, Clinical Research, Clinical Study Design, Clinical Trial Compliance, Clinical Trials, Clinical Trials Analysis, Data Analysis, Drug Development, ICH GCP Guidelines, Ophthalmology, Regulatory Compliance, Strategic Thinking. Under the direction of the Program Lead, you will collaborate with global cross functional team members including clinical directors and study managers to lead/support clinical trial scientific activities.

New!

Princeton, NJ2 days ago

$173,390–$210,110 Per Year

p>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/.

Madison, NJ11 days ago

$173,390–$210,110 Per Year

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/.

New!

Rahway, NJ2 days ago

$117,000–$184,200 Per Year

p>Co-authors clinical sections of protocols, clinical investigator brochures, clinical study reports, Worldwide Marketing Application/Common Technical Document (WMA/CTD) subsections, and regulatory agency update and safety reports, as well as clinical development plans, publications, and abstracts.

Experience managing Immunology and/or vaccine trials with an ability to think outside of the box, explore novel ways of working and comfortably navigate ambiguity to drive results also a plus.

Rahway, NJ28 days ago

$117,000–$184,200 Per Year

Other responsibilities include: Collaborating cross-functionally in the development of Protocol and related study materials (e.g., ICF documents/amendments); Partners with the Study Manager on study deliverables. Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities.

Princeton, NJ23 days ago

Full-time

Work in close collaboration with the clinical team to ensure translation of the clinical protocol (and amendments) into operational deliverables, including but not limited to performing ongoing review and analysis of clinical study data and preparing/reviewing study plans (i.e., Medical Monitoring, Medical Data Review, Safety Management, CRF Completion Guidelines, etc.). This role provides an excellent opportunity to gain hands-on experience in clinical trial design and execution while working alongside experienced clinical development professionals in a dynamic biotech/pharmaceutical environment.

Princeton, NJ24 days ago

$80,000–$130,000 Per Year

li>Work in close collaboration with the clinical team to ensure translation of the clinical protocol (and amendments) into operational deliverables, including but not limited to performing ongoing review and analysis of clinical study data and preparing/reviewing study plans (i.e., Medical Monitoring, Medical Data Review, Safety Management, CRF Completion Guidelines, etc.). This role provides an excellent opportunity to gain hands-on experience in clinical trial design and execution while working alongside experienced clinical development professionals in a dynamic biotech/pharmaceutical environment.

Princeton, NJ30+ days ago

$200,000–$250,000 Per Year

p>Develops and provides input for clinical presentation slides and other materials for internal/external meetings and/or ongoing communications (e.g., investigator meetings, pre-study site selection visits, study coordinator or clinical research administrator training, study newsletters, communications to study sites, etc.).

HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI.

Rahway, NJ8 days ago

$282,200–$444,200 Per Year

li>Assist the Senior/Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our Company's and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility.

Monitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed Oncology drugs;

Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; and.

Rahway, NJ30+ days ago

$282,200–$444,200 Per Year

Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our company and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility.

Required Skills:

Clinical Development, Clinical Medicine, Clinical Research Management, Clinical Studies, Clinical Trial Development, Clinical Trials, Dermatology, Drug Development, Gastroenterology, Inflammatory Bowel Diseases, Pharmaceutical Industry, Regulatory Compliance, Rheumatology.

Rahway, NJ13 days ago

$282,200–$444,200 Per Year

li>Assist the Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our Company's and competitors' drugs and internal and external expert opinion on scientific questions relevant to their areas of responsibility.

The Senior Director is responsible for maintaining a strong scientific fund of knowledge by:

Maintaining awareness of scientific developments within their area of expertise, in terms of new scientific findings, research methodologies.

Rahway, NJ29 days ago

$96,200–$151,400 Per Year

Job Responsibilities: Responsible for specific clinical/scientific activities on a single study or across multiple studies (e.g., medical monitoring, lab specimen tracking/reconciliation, adjudication support, preparation of meeting materials). Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities.

New!

Rahway, NJ1 day ago

$142,400–$224,100 Per Year

p>Translational Medicine (TMed) drives early clinical development of novel therapeutics by partnering with Discovery Sciences and Late-Stage Clinical Research to translate scientific discoveries into human proof-of-concept and advance the most promising candidates through the pipeline to patients.

Leads and directs teams through key study planning, development, and execution activities, including program overviews, issue escalation and mitigation, senior management presentations, cross-functional governance meetings, and advisory meeting preparation.

Raritan, New Jersey30+ days ago

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Ensures team member adherence to clinical research guidelines and safety procedures;

Communicates detailed outcomes and results of research findings to relevant partners;

Provides input in managing project budgets and projections;

Serves as liaison to global clinical sites for medical questions related to the clinical research trial ;

Presents study status at internal/external meetings, including investigator meetings and governance committees. Clinical Evaluations, Corrective and Preventive Action (CAPA), Drug Discovery Development, Entrepreneurship, Good Clinical Practice (GCP), Leadership, Medicines and Device Development and Regulation, Presentation Design, Regulatory Affairs Management, Relationship Building, Research Documents, Safety-Oriented, Scientific Research, Strategic Change, Study Management, Tactical Planning, Technical Credibility

Rahway, NJ30+ days ago

$255,800–$402,700 Per Year

The Clinical Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within their area of expertise, in terms of new scientific findings, research methodologies. Job Description: The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Immunology therapeutic area.

New!

NJ4 days ago

Full-time

Experiences in metabolic diseases (Diabetes, Obesity, NASH, NAFLD, etc.), Endocrinology (CKD, CRF, etc.), and Nutrition and Weight Management related drug development are a plus. The position will work with Gan & Lee clinical program lead(s) to provide the scientific and clinical leadership and inputs in meeting the development objectives for the program.

Bridgewater, NJ15 days ago

$100.50–$145.17 Per Hour

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Minimum 4-5 years for Master's degree holder or 2-4 years for Doctoral degree holder of relevant experience in real-world data, commercial analytics, real-world evidence, health outcomes research, fit-for-purpose feasibility assessment, data quality assessment or a related field within the pharmaceutical, biotech, or health technology industry. This role serves as a methodological authority and RWD data domain expert, ensuring best-in-class data selection and optimal data usage to generating reliable insights or evidence to better understanding gaps in patient care and healthcare providers involved in patient care.

Rahway, NJ30+ days ago

$173,200–$272,600 Per Year

PSCS #eligibleforERP #FLEx2026 #NSBE2026 Required Skills: Clinical Manufacturing, Creativity, Cross-Functional Teamwork, Decision Making, Downstream Processing, Driving Continuous Improvement, Manufacturing Scale-Up, Mentorship, Process Characterization, Process Control, Process Design, Process Optimization, Regulatory Submissions, Strategic Thinking, Technology Transfer Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Has knowledge of formulation science and in-depth knowledge in multiple areas, including core understanding of the drug development process, excipient attributes, and formulation-process interplay Demonstrated understanding of connectivity between clinical development, chemistry, manufacturing and control (CMC) and commercial marketing, balancing the needs of patients and ensuring successful launch of drug products Experience leading development projects at an enterprise level Strong mentoring capabilities to build individuals and teams.

Philadelphia, PA30+ days ago

p>Responsibilities: Key Responsibilities: Serve as a key clinical science contributor for assigned CAR-T programs, partnering with the Medical Director and other Clinical Development team members to support study design, execution, and interpretation across all phases of clinical development. Lead or contribute to the preparation of key clinical documents - including protocols, amendments, informed consent forms, investigator brochures, clinical study reports, and regulatory submissions (e.g., INDs, CTAs, DSURs, BLAs/MAAs).

Somerset, NJ30 days ago

$127,313–$167,099 Per Year

Contribute to the planning and execution of external meetings and internal stakeholder meetings (e.g., Ad Boards, IMs, Governance, DMCs, Regulatory Authority, Dose Escalation meeting); responds to or triages questions for appropriate escalations.

Rahway, NJ30+ days ago

$282,200–$444,200 Per Year

The Senior Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies. The Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new medicines in the Oncology Asset therapeutic area.

Princeton, NJ10 days ago

$211,910–$256,789 Per Year

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/.

Spring House, PA8 days ago

Remote

$58–$59 Per Hour

This global role offers a unique opportunity to apply advanced analytics to real-world data (RWD) and contribute to the generation of evidence that informs clinical development, regulatory strategy, and healthcare decision-making across diverse populations and geographies. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

Spring House, PA8 days ago

Remote

p style="font-family:'calibri';font-size:10pt">The Real-World Evidence (RWE) team within Innovative Medicine is seeking a highly motivated Postdoctoral Scientist to join our Data Science & Digital Health (DSDH) Immunology group. This global role offers a unique opportunity to apply advanced analytics to real-world data (RWD) and contribute to the generation of evidence that informs clinical development, regulatory strategy, and healthcare decision-making across diverse populations and geographies.

Spring House, PA8 days ago

Remote

$58–$58.81 Per Hour

This global role offers a unique opportunity to apply advanced analytics to real-world data (RWD) and contribute to the generation of evidence that informs clinical development, regulatory strategy, and healthcare decision-making across diverse populations and geographies. The Real-World Evidence (RWE) team within Johnson & Johnson Innovative Medicine is seeking a highly motivated Postdoctoral Scientist to join our Data Science & Digital Health (DSDH) Immunology group.

Spring House, PA8 days ago

Remote

$55–$58.39 Per Hour

This global role offers a unique opportunity to apply advanced analytics to real-world data (RWD) and contribute to the generation of evidence that informs clinical development, regulatory strategy, and healthcare decision-making across diverse populations and geographies. The Real-World Evidence (RWE) team within Pharmaceutical Innovative Medicine is seeking a highly motivated Postdoctoral Scientist to join our Data Science & Digital Health (DSDH) Immunology group.

Raritan, NJ30+ days ago

$122,000–$212,000 Per Year

Ensures team member adherence to clinical research guidelines and safety procedures; Communicates detailed outcomes and results of research findings to relevant partners; Provides input in managing project budgets and projections; Serves as liaison to global clinical sites for medical questions related to the clinical research trial ; Presents study status at internal/external meetings, including investigator meetings and governance committees. Required Skills: Preferred Skills: Clinical Evaluations, Corrective and Preventive Action (CAPA), Drug Discovery Development, Entrepreneurship, Good Clinical Practice (GCP), Leadership, Medicines and Device Development and Regulation, Presentation Design, Regulatory Affairs Management, Relationship Building, Research Documents, Safety-Oriented, Scientific Research, Strategic Change, Study Management, Tactical Planning, Technical Credibility.

Summit, NJ16 days ago

$55.67–$78.60 Per Hour

D. ( preferred) in Data Sciences, Computational & Integrative Sciences or equivalent , with proven track record (e.g publications, posters, presentations) of applying modeling, simulation, and computational approaches for real world academic or industry toxicology/health sciences studies.

In this role, you will leverage advanced computational, omics, and data science approaches to support pre-clinical safety and product development decisions, integrating AI and machine learning tools to accelerate insights and enhance scientific workflows.

Princeton, NJ30+ days ago

Clinical Research - Ligand Binding Analytical Scientist I in Princeton, NJ - Syneos Health Apply Inside Syneos Health Our Values Who We Are Our Solutions Diversity, Equity, And Inclusion Why Work Here Discover what our more than 29,000 employees already know: work here matters everywhere. Together we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients.

Princeton, NJ30+ days ago

Together we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to:

Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.

Flemington, NJ13 days ago

Travel Nurse Across America is seeking a qualified Clinical Lab Scientist LAB needed for travel nurse assignment in Flemington, NJ. This assignment is in a Traveler-friendly facility and offers excellent pay, benefits, bonus opportunity, travel reimbursement, all licenses and certifications paid and more!

Iselin, New Jersey24 days ago

Remote

p>If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at . This role is heavily focused on hands-on laboratory work, with the primary responsibility centered on the technical execution of complex R&D experiments, design and execution of validation studies, and continuous improvement of existing assays and workflows.

Rahway, NJ10 days ago

$210,400–$331,100 Per Year

p>In a competitive external landscape and fast-paced internal environment, the Immunology Clinical Operations Lead position provides both strategic and operational leadership across early immunology programs, ensuring timely, high-quality execution of clinical studies and clinical pharmacology strategies worldwide.

Translational Medicine (TMed) drives early clinical development of novel therapeutics by partnering with Discovery Sciences and Late-Stage Clinical Research to translate scientific discoveries into human proof-of-concept and advance the most promising candidates through the pipeline to patients.

Princeton, NJ28 days ago

For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. Please note that if you are applying for a position in the Netherlands, Genmab's policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract.

Somerset, NJ30+ days ago

Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. Leverage advanced single-cell technologies (e.g., scRNA-seq) to deeply profile immune cell compartments, particularly T-cell states and exhaustion markers, to inform patient stratification and biomarker hypotheses.

Somerset, NJ9 days ago

$146,410–$192,164 Per Year

Iselin, NJ23 days ago

Remote

$90,000–$129,000 Per Year

This role is heavily focused on hands-on laboratory work, with the primary responsibility centered on the technical execution of complex R&D experiments, design and execution of validation studies, and continuous improvement of existing assays and workflows. The ideal candidate will bring deep expertise in next-generation sequencing (NGS) and other high-complexity genomic technologies, along with strong analytical and technical writing capabilities.

Summit, New Jersey17 days ago

p style="text-align:inherit"/>

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.

Kenvue is currently recruiting for a:

Pre Clinical Safety Data Scientist

What we do.

Livingston, NJ14 days ago

$31.59–$39.52 Per Hour

Our primary, multispecialty, and urgent care providers serve millions of patients in traditional practices, patients' homes and virtually through VillageMD and our operating companies Village Medical, Village Medical at Home, Summit Health, CityMD, and Starling Physicians. We are innovating value-based care and leveraging integrated applications, population insights and staffing expertise to ensure all patients have access to high-quality, connected care services that provide better outcomes at a reduced total cost of care.

Princeton, NJ24 days ago

$184,060–$223,036 Per Year

Key Responsibilities:

Designs and implements program-specific late development biomarker/translational plans, responsible for aiding in creation of clinical protocols, SAPs, SOWs, lab manual, and interfacing with CRO for execution of services, in conjunction with Biospecimen Operations and Procurement.

NJ30+ days ago

$310,900–$489,400 Per Year

Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, medical affairs, and manufacturing to manage clinical development projects; and assist the Section Head in ensuring that appropriate Corporate personnel is informed of the progress of studies of our company and competitors drugs and internal and external expert opinion on scientific questions relevant to their areas of responsibility.

Must have experience in industry in the field of Thoracic Oncology Minimum of 3 years of clinical medicine experience Minimum of 5 years of industry experience in drug development Demonstrated record of scientific scholarship and achievement A proven track record in clinical medicine and background in biomedical research is essential Strong interpersonal skills, as well as the ability to function in a team environment, are essential.

NJ30+ days ago

$342,800–$539,600 Per Year

The Associate Vice President (AVP) ensures that Clinical Scientists deliver consistent, high quality‑ scientific and technical oversight of studies and assets, partnering closely with Clinical Directors (CDs), Product Development Team Leaders, Therapeutic Area Heads, Global Clinical Trials operations teams as well as other cross functional partners to advance programs from First-In-Human‑through registration and lifecycle management. Required Skills: Biostatistics, Client Management, Clinical Judgment, Clinical Research Methods, Conflict Resolution, Detail-Oriented, Innovation, Multiple Therapeutic Areas, Negotiation, New Technology Integration, People Leadership, Pharmacovigilance, Protocol Development, Strategic Planning, Visionary Leadership.

NJ30+ days ago

Remote

$117,000–$201,250 Per Year

p>All Job Posting Locations:

Cambridge, Massachusetts, United States of America, Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America.

Work with Data Science & Digital Health colleagues, IT and DevOps teams to deploy and manage the graph database infrastructure, focusing on high availability, scalability, and recovery operations specifically geared toward Immunology R&D needs and applications.

Titusville, New Jersey30+ days ago

Remote

Job Description:.

Raritan, NJ30+ days ago

All Job Posting Locations: Cambridge, Massachusetts, United States of America, Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America. Work with Data Science & Digital Health colleagues, IT, and DevOps teams to deploy and manage the graph database infrastructure, focusing on high availability, scalability, and recovery operations specifically geared toward Oncology R&D needs and applications.

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Clinical Scientist Jobs in Princeton, NJ

Senior Director, Clinical Safety Scientist Daiichi Sankyo, Inc.

Associate Scientist Joulé

Senior Director, Clinical Safety MD Daiichi Sankyo, Inc.

Job Description.

Senior Formulation Scientist Aquestive Therapeutics Inc.

Sr. Clinical Scientist/Associate Director, Clinical Science Celldex Therapeutics Inc

Senior Scientist, Clinical Operations - Ophthalmology Merck & Co Inc

Senior Manager, Global Clinical Scientist (Cell Therapy) Bristol-Myers Squibb Co

Senior Manager, Global Clinical Scientist - Psychiatry Bristol-Myers Squibb Co

Senior Scientist, Clinical Research Merck & Co Inc

Sr. Scientist, Clinical Operations Merck & Co Inc

Clinical Scientist Systimmune

Clinical Scientist Systimmune Inc

Director, Clinical Scientist Summit Therapeutics Inc

Senior Principal Scientist, Clinical Research, Breast Cancer Merck & Co Inc

Senior Principal Scientist, Clinical Research, Immunology Merck & Co Inc

Senior Principal Scientist, Clinical Research, GI Merck & Co Inc

Scientist, Clinical Operations Merck & Co Inc

Associate Principal Scientist, Clinical Research Merck & Co Inc

Assoc Dir Clinical Scientist Oncology Johnson & Johnson

Clinical Director (Principal Scientist), Clinical Research, Immunology - Rheumatology Merck & Co Inc

Senior Manager, Clinical Scientist Gan & Lee Pharmaceuticals

Clinical Data Scientist/ Methodologist Sanofi

Principal Scientist, Technical Director - Process Engineering - Oral Solid Dosage, Clinical Manufacturing (Onsite) Merck & Co Inc

Director, Clinical Scientist Cabaletta Bio Inc

Senior Clinical Research Scientist Legend Biotech Corp

Senior Principal Scientist (Senior Director), Clinical Research, ADC Merck & Co Inc

Associate Director, Global Clinical Scientist (Cell Therapy) Bristol-Myers Squibb Co

Scientist 3 - Clinical Research eTeam Inc.

Scientist 3 - Clinical Research Ampcus Incorporated

Scientist 3 - Clinical Research Net2Source

Scientist 3 - Clinical Research Artech LLC

Associate Director, Clinical Project Scientist, Oncology Johnson & Johnson

Pre Clinical Safety Data Scientist Kenvue Inc

Clinical Research - Ligand Binding Analytical Scientist I Syneos Health Inc

Ligan Binding Research Scientist - Clinical Research Syneos Health Inc

Travel Clinical Lab Scientist (CLS) in Flemington, NJ TNAA | TotalMed

Scientist II - Clinical Genomics Labcorp

Sr. Principal Scientist, Clinical Operations Immunology Lead Merck & Co Inc

Senior Clinical Research Scientist Genmab AS

Principal Scientist, Clinical Biomarker, Immunology, Immuno-Oncology, & Hematology Contractor Legend Biotech Corp

Principal Scientist, Clinical Biomarker, Immunology & Immuno-Oncology Hematology Legend Biotech Corp

Scientist II - Clinical Genomics Labcorp Holdings Inc

Pre Clinical Safety Data Scientist Kenvue

Clinical Lab Scientist - STAT Lab Summit Health Inc

Senior Principal Scientist, Neuroscience, Clinical Biomarker, Late Phases, Translational Medicine Bristol-Myers Squibb Co

Distinguished Scientist, Clinical Research, Thoracic Malignancies Merck & Co Inc

AVP, Head of Infectious Disease & Vaccines Clinical Science Merck & Co Inc

Principal Data Scientist - Immunology - (2 positions) Johnson & Johnson

Principal Data Scientist - Immunology - (2 positions) 6084-Janssen Research & Development Legal Entity

Principal Data Scientist - Oncology Johnson & Johnson

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