160 Results for

Clinical Scientist Jobs in Princeton, NJ

Jobs

Bernards, NJ13 days ago

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. In addition to operational oversight, this role contributes to the development of global safety processes, talent capability building, and strategic alignment across the broader Clinical Safety and Pharmacovigilance (CSPV) function and the enterprise.

Rahway, NJ11 days ago

$45–$53.45 Per Hour

Serve as a subject matter expert in immunoassay-based assay development and validation, collaborating with project teams, biomarker leaders, clinical operations and regulatory affairs on the implementation of these assays in clinical trials. Translational Molecular Biomarkers (TMB) is responsible for the development and execution of clinical biomarker assays across all therapeutic areas and all phases of clinical development within our company's research laboratories.

Plainsboro Township, New Jersey11 days ago

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. Manage pre-, peri-, and post-congress activities, including communications, scheduling, meeting debriefs, and insights gathering for strategic dissemination.

Princeton, NJ11 days ago

Collaborative team player who is highly self-motivated, with a proven ability to learn quickly and thrive in dynamic, high-impact environments. Understand clinical needs to solve real-world problems and drive the design, development, and validation of new AI clinical solutions.

Holmdel, NJ23 days ago

Full-time
Employee

Provides support to the department in the areas of quality control, troubleshooting complex problems, customer support, instrument and equipment maintenance, staff training, process improvement and the completion of special projects as assigned. Perform test procedures of moderate/high complexity requiring the exercise of independent judgement and responsibility in those specialties in which they are qualified by education, training and experience.

Rahway, NJ27 days ago

Temporary
Contractor
Full-time

D. degree in chemistry, biochemistry or related scientific discipline with 5 years of industrial experience, OR Master of Science degree in chemistry, biochemistry or related scientific discipline with at least 10 years of industrial experience, preferably in a bioanalytical laboratory. Develop, validate and implement LC-MS/MS assays for the analysis of tissue, plasma and other biological samples to support pharmacokinetic, toxicokinetic, clinical efficacy and/or human food safety studies in a GLP environment.

New!

Bernards, NJ1 day ago

The individual assuming this role may function as a key member of the Global Product Team in collaboration with Clinical Development, Regulatory, Project Management, Biostatistics, Pharmacology, and other departments to strategically manage benefit-risk throughout the lifecycle of the drug. Depending on the status of development of the compound, lead and medical-scientifically direct a team of physicians and scientists responsible for a compound/product including project-specific training and coaching of team members and review of team output cross-functionally.

Camden, NJ7 days ago

The ideal candidate must be experienced in general urology conditions with a special emphasis to include benign prostatic hypertrophy (BPH), urinary stone disease, and lower urinary tract symptoms (LUTS). The Department of Surgery at Cooper University Hospital is seeking to hire a full-time urologist who has completed an accredited residency in Urology and whose primary focus is on the evaluation and management of common urologic conditions (general urology).

Philadelphia, PA7 days ago

Yuliana Salamanca-Padilla, Interim Chair, C/O Bill Mawhinney, Senior Recruiter, Office of Physician/Faculty Recruitment & Retention Lewis Katz School of Medicine at Temple University, Email: The University is especially interested in qualified candidates who can contribute through their research, teaching, and/or service to the diversity and excellence of the academic community. • Clinical: Temple Health's program provides an opportunity to work in high volume inpatient and outpatient procedural anesthetic services with a case mix of trauma, vascular, transplants, orthopedic, and neurosurgical cases.

Trenton, NJ30+ days ago

Author/review clinical contributions to clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., Pre-IND, IND, IB, DSUR, PSUR, Orphan Annual Reports, HA, EC, IRB responses and contribute to regulatory submission.). • Collaborate cross-functionally to develop Protocol and ICF documents / amendments and present these to governance committee and early clinical development team meetings as required.

New!

Piscataway, NJ6 days ago

Remote

The ideal candidate will bring deep expertise in oncology clinical development, with strong experience in late-phase studies and cross-functional leadership. Author and review key documents including protocols, investigator brochures, clinical study reports, and regulatory submissions (INDs, CTAs).

Trenton, NJ30+ days ago

Remote

$71,100–$97,800 Per Year

To ensure Home or Hybrid Home/Office employees’ ability to work effectively, the self-provided internet service of Home or Hybrid Home/Office employees must meet the following criteria: + At minimum, a download speed of 25 Mbps and an upload speed of 10 Mbps is required; wireless, wired cable or DSL connection is suggested. The Clinical Analytics team identifies opportunities and build solutions to improve clinical outcomes and lower costs for millions of Medicare Advantage beneficiaries leveraging data science & analytics, clinical expertise, strategic mindset, and rigorous study designs.

Madison, NJ30+ days ago

The Worldwide Patient Safety group is responsible for ensuring the safety of our medicines: The Worldwide Patient Safety group is responsible for pharmacovigilance and pharmaco-epidemiology deliverables including single case and aggregate safety monitoring, safety reporting, contribution to benefit-risk assessment, risk management planning and strategy, and execution of certain post-marketing commitments and ensuring compliance with global regulatory requirements. • Author responses to safety data queries from health authorities including coordination and integration of scientific, medical, and regulatory input from a variety of scientific sources and functional groups, as needed to support responses to safety data/ad hoc queries and HA requests.

Philadelphia, PA30+ days ago

Summary: Performs waived, moderate and/or high-complexity tests and procedures in clinical laboratory sections under the direction of the Supervisor.•Performs appropriately requested clinical laboratory analyses on all types of laboratory specimens, produces and documents accurate laboratory results for diagnosis and treatment of disease.•May be required to perform phlebotomy for diagnostic testing on patients of all age groups. Education Specialization: in MLS or other biological or chemical science or U.S. equivalent (substantiated by foreign credential evaluation statement) Equivalent Experience: •And Broad knowledge of various laboratory methods and techniques, quality assurance, in addition to PC and LIS knowledge .

Philadelphia, PA30+ days ago

New!

Philadelphia, PA6 days ago

Works well with Supervisors and those in authority; works at establishing a good rapport and cooperative working relationship with all members of the laboratory; maintains a positive rapport with medical staff and hospital personnel. Perform appropriately requested clinical laboratory analyses on all types of laboratory specimens, produces and documents accurate laboratory results for diagnosis and treatment of disease.

Philadelphia, Pennsylvania30+ days ago

Responsibilities: Works with the MAC System Engineer and Physical Therapist to develop new clinical lines of service, business plans or research grants/projects that improves quality of care, expands the population the MACs service, and develops new technologies. Located in North Philadelphia on the Main Campus of Temple University Hospital, Shriners Children's Philadelphia is a 49-bed pediatric specialty hospital dedicated to providing comprehensive care for children with orthopedic conditions and spinal cord injuries.

Philadelphia, PA30+ days ago

The incumbent's additional responsibilities will include, but are not limited to, performing waived, moderate, and/or high-complexity tests and procedures in clinical laboratory sections, performing appropriately requested clinical laboratory analyses on all types of laboratory specimens, and documenting accurate laboratory results for the diagnosis and treatment of disease. Penn Medicine is dedicated to our tripartite mission of providing the highest level of care to patients, conducting innovative research, and educating future leaders in the field of medicine.

Philadelphia, PA30+ days ago

Education or Equivalent Experience: Bachelor of Arts or Science (Required)in MLS or other biological or chemical science or U.S. equivalent (substantiated by foreign credential evaluation statement) with broad knowledge of various laboratory methods and techniques, quality assurance, in addition to PC and LIS knowledge. Performs appropriately requested clinical laboratory analyses on all types of laboratory specimens, produces and documents accurate laboratory results for diagnosis and treatment of disease.

Philadelphia, PA30+ days ago

Bachelor of Arts or Science (Required) in MLS or other biological or chemical science or U.S. equivalent (substantiated by foreign credential evaluation statement) with broad knowledge of various laboratory methods and techniques, quality assurance, in addition to PC and LIS knowledge. Performs appropriately requested clinical laboratory analyses on all types of laboratory specimens, produces and documents accurate laboratory results for diagnosis and treatment of disease.

Trenton, NJ30+ days ago

Leveraging your profound expertise in graph databases (e.g., Neo4j, ArangoDB, Amazon Neptune, Ontotext GraphDB), distributed graph processing frameworks (e.g., Apache Spark GraphX, Dask-Graph), and leading GML libraries (e.g., PyTorch Geometric, DGL, Spektral), you will conduct in-depth research, construct sophisticated predictive, prescriptive, and diagnostic models directly on graph structures. You will proactively identify opportunities to construct and leverage comprehensive healthcare knowledge graphs, integrating diverse patient, provider, claims, and clinical data to uncover hidden patterns, propagate insights through networks, and develop groundbreaking analytical solutions that exploit the rich, multi-modal structures within healthcare.

Lawrenceville, New Jersey21 days ago

£65,977–£82,472

Experimental techniques could include, but are not limited to, the following: Processing human tissue and blood, Cell-based assays, Flow cytometry, ELISAs/MSD assays, RNA extraction and cDNA synthesis, Gene expression array cards. The qualified candidate will process human samples, maintain the laboratory's biobank (including sample storage and retrieval), and perform a range of experimental procedures under the guidance of senior scientists.

Princeton, NJ30+ days ago

$160,060–$193,900 Per Year

Key responsibility of this role is to effectively collaborate with a cross functional team of asset scientists with deep disease, drug development and business knowledge to help drive an overall translational strategy, working closely with discovery and early development teams, late clinical development as well as with our team of laboratory scientists. + Leads small and large collaborations with academia and industry partners to identify biobanks, clinical trials and existing databases to collate multi-parameter genomic, immune and clinical datasets to mine for novel biomarkers of unmet need patients in conjunction with computational biologists, data scientists and statisticians.

Princeton, NJ30+ days ago

$112,000–$140,000 Per Year

New Brunswick, NJ30+ days ago

$136,960–$165,964 Per Year

Located at our either our New Brunswick or Lawrenceville facilities in NJ, the exceptional organic chemist joining our Chemical Process Development organization will: Lead chemistry teams to deliver disruptive science, novel chemical routes, robust and well characterized manufacturing processes and outstanding scientific knowledge to support the development and commercialization of our portfolio. 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.

Summit, NJ30+ days ago

$140,000–$165,000 Per Year

This individual will work on cross-functional project teams to drive execution of translational/biomarker plans working with laboratory and disease scientists and BMS members from clinical, medical, commercial, regulatory and diagnostics as well as engage external academic collaborators/Key opinion leaders (KOLs). Key responsibilities of this role are to act as a lead scientist to deliver and implement biomarker strategies for clinical programs, develop reports and publications on preclinical and translational data generated to support asset development and contribute to regulatory submissions.

New Brunswick, NJ30+ days ago

$134,900–$163,461 Per Year

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. PhD in Immunology, Cell Biology, Molecular Biology, or a related scientific discipline with 4–6 years of relevant industry experience; or a Master’s degree with 6–9 years of experience; or a Bachelor’s degree with 9–12 years of experience.

New!

Philadelphia, PA5 days ago

Philadelphia, PA30+ days ago

New Brunswick, NJ30+ days ago

$23–$42 Per Hour

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. In this position, you will directly support operational projects including transferring critical documents into an electronic repository, data entry into inventory systems, cataloging materials, subdividing RSCR materials, and working with our Scientists on various activities within our laboratory.

Summit West, NJ30+ days ago

$82,420–$99,879 Per Year

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. This includes execution of thorough root cause investigations, interviewing personnel, hypothesis testing and interpretation of results, authoring investigation reports, identifying corrective and preventive actions (CAPA), and troubleshooting complex problems.

Camden, NJ13 days ago

Directly accountable to the Primary Investigator, the Research Scientist will conduct specific research projects related to stroke and Traumatic Brain Injury (TBI) recovery. Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols.

Warren, NJ10 days ago

$115,000–$125,000 Per Year
Full-time

Good understanding of formulation development principles, DoE/QbD and FDA/CMC/ICH guidelines are required Regulatory document authoring experience is required Must have an ability to work on multidisciplinary teams to drive innovation that leads to commercially viable products/technologies. Experience in alternate delivery of drugs (oral, transmucosal, topical) preferred Strong background in formulation design, optimization, and characterization Hands-on expertise with experimental design, data analysis, and statistical tools.

Philadelphia, PA30+ days ago

Located in the Chestnut Hill section of Philadelphia, Temple Health - Chestnut Hill Hospital, an alliance of Temple Health, Redeemer Health and PCOM, is a 148-bed, community-based, university-affiliated, teaching hospital committed to excellent patient-centered care. With more than 300 board-certified physicians, Chestnut Hill Hospital's specialties include minimally invasive laparoscopic and robotic surgery, cardiology, gynecology, oncology, orthopedics, urology, pulmonology, cancer care, family practice and internal medicine.

Philadelphia, PA30+ days ago

Philadelphia, PA18 days ago

New Brunswick, NJ30+ days ago

This individual will focus on the timely and quality ordering, receipt, storage of lab supplies, inventory tracking, lab instrumentation maintenance including freezers, pH meters, balances, pipettes, HPLC, UPLC, and Capillary Electrophoresis (CE) systems. Additionally, the assistant QC Chemist will be responsible for continuous improvement of the lab management processes from the New Brunswick and Summit West methods development laboratories.

Summit, NJ30+ days ago

Position Description: The selected candidate will have primary responsibility of developing mammalian cell lines to produce fusion proteins, or other recombinant proteins, for clinical and commercial manufacturing. Client Biologics Development has a Cell Line Development and 'Omics organization that includes Molecular Biology, Cell Line Development, and Multi-Omics.

Princeton, NJ30+ days ago

$145,320–$176,100 Per Year

We are looking for candidates with strong computational, statistical, and biological capabilities with a demonstrated track record of translating complex data into testable hypotheses and experience modeling multimodal (clinical, omics, real-world data) using the classical ML and Deep Learning algorithms. 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.

Princeton, NJ30+ days ago

$217,520–$263,577 Per Year

Risk Management Planning & Execution: Creates strategy for creation and update of the EDSR to proactively characterize emerging safety concerns during asset development, support Structured Benefit Risk, and define the strategy for Company Core Risk Management and gaining alignment with SMT/governance, including collaboration with Epidemiology on risk minimization effectiveness, non-interventional research (NIR) activities for post-authorization safety studies (PASS). The Director, Patient Safety Scientist, is a key partner and strategic advisor to Medical Safety Assessment Physician (MSAP)/Safety Management Team (SMT) Chair to characterize conditions for safe use of BMS medicines and proactively communicate safety evidence to influence decision-making for assets in development and marketed products by evaluating and mitigating risks.

Princeton, NJ30+ days ago

$152,730–$185,100 Per Year

In this role, you will represent the Dev DMPK function on cross-functional development project teams; oversee developmental drug metabolism and disposition, and non-clinical pharmacokinetics activities of multiple projects; be responsible for preparation of regulatory dossier / submissions; and assist in developing strategy for the group. Within the Pharmaceutical Candidate Optimization (PCO) organization at BMS, the Development DMPK Team provides ADME (absorption, distribution, metabolism, and excretion), DDI (drug-drug interactions) and PK (pharmacokinetics) support for all pipeline assets throughout clinical development, from candidate nomination through registration and lifecycle management.

Princeton, NJ30+ days ago

$87,810–$106,399 Per Year

The Development Data Scientist Analyst will play a crucial role in supporting study clinical operational analytics across Drug Development to ensure products continue to serve most pressing DD analytics needs, with opportunities to build new advanced analytics capabilities such as predictive modelling, simulation, and optimization. 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.

Summit, NJ30+ days ago

Prior hands-on experience with downstream process development, including preparative chromatography, ultrafiltration/diafiltration, viral inactivation, viral filtration and high throughput robotic platforms is desired. • B.S. in Chemical/Biochemical Engineering, Biotechnology, Biochemistry, or related biologics fields with 0 - 2 years of industry experience is required.

New Brunswick, NJ30+ days ago

$104,300–$126,400 Per Year

Work-life programs include paid national holidays and optional holidays, Global Shutdown days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. CPD scientists focus on developing safe, economical, sustainable, and robust processes to support clinical trials and the launch of new medicines across various drug modalities including small molecules, peptides, oligonucleotides, and antibody drug conjugates.

Philadelphia, PA30+ days ago

Develop bench scale suspension culture processes for viral vector generation within shake flasks and bioreactors through design and execution of experiments to support process characterization, and process transfer activities between the research team, TechOps, and external partners. Responsibilities will include, but are not limited to, performing the day-to-day activities of the viral process development lab, building Client's viral manufacturing capabilities, and executing experiments to support viral process development/characterization.

Princeton, NJ30+ days ago

$138,850–$168,300 Per Year

Work-life programs include paid national holidays and optional holidays, Global Shutdown days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. The group supports the BMS portfolio through all stages of discovery and development with stage-appropriate, hypothesis driven, in vitro and in vivo transporter assessments; applying mechanism-based approaches to the quantitative translation of pre-clinical in vitro and in vivo data to clinical findings.

Raritan, NJ30 days ago

Remote

Full-time

The Senior Scientist, Biostatistics will support the Oncology Therapeutic Area with a focus on: solid tumors or hematologic malignancies; cancer interception with the goal of developing products that interrupt the carcinogenic process; biomarkers that may help guide targeted, individualized use of our therapies; as well as safe and effective identification and treatment of early changes in the tumor microenvironment. 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.

Trenton, NJ30+ days ago

Develop IEP(s) that reflects asset strategy, market priorities and medical evidence generation support (investigator vs company sponsored research) in partnership with the Immunology and Neuroscience Global Medical Disease Team and cross-functional teams including (but not limited to) Global Drug Development (GDD), Translational Development, Health Economics and Outcomes Research (HEOR), and others. • Responsible for ongoing Immunology and Neuroscience ISR work, including non-clinical research studies and serve as the subject matter expert and interface with all key stakeholders across the matrix, including (but not limited) to Worldwide and Local Medical, Global Development Operations (GDO), GDD, Field Medical, Commercial, and HEOR.

Spring House, PA30+ days ago

Full-time

BS or MS degree in Chemical Engineering, Biomedical Engineering, Biological Sciences, Chemistry, Biochemistry, or other equivalent and background with 6-8 years of experience is required; or a PhD with 4+ years of post-doctoral and/or relevant industry experience is highly preferred. You will identify and conceptualize new ideas, designing, planning and leading experiments, prioritizing areas of focus based on business objectives, and analyzing complex issues by problem-solving and turning solutions into reality.

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Clinical Scientist Jobs in Princeton, NJ

Jobs

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