91 Results for

Drug Safety Jobs in Somerville, NJ

Jobs

Senior Director Clinical Safety MD Daiichi Sankyo, Inc.

Basking Ridge, NJ

$280,350–$467,250 / year
Full time

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.

30+ days ago

Senior Director, Clinical Safety MD Daiichi Sankyo, Inc.

Basking Ridge, NJ

$280,350–$467,250 / year
Full time

30+ days ago

Associate Director, Global Drug Safety & Pharmacovigilance Scientist Genmab AS

Princeton, NJ

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. Contribute to safety-related documents for Genmab products throughout product lifecycle from FIH to post-marketing, including robust safety surveillance, Safety Assessment Reports for potential signals/risks, RSI in IB, ADR in the CCDS and product labels, Aggregate Safety Reports (e.g.

30+ days ago

Director, Global Drug Safety & Pharmacovigilance Physician Genmab AS

Princeton, NJ

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. You will work together with other Drug Safety staff in managing the safety assessment of products, including review of individual and aggregate AEs and the scientific literature, preparing safety reports, and communicating changes in the product risk profile to internal and external stakeholders supporting the Team Lead.

30+ days ago

Vice President and Global Head of Drug Safety and Pharmacovigilance Insmed Inc

Remote

$365,000–$497,000 / year

As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you'll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person's contributions to meaningful progress. Who You Are: You must have an MD with 15+ years of drug development experience within a pharmaceutical or biotech company, 10+ years of pharmacovigilance (PV)/drug safety leadership, and a minimum of 5 years' experience as a VP or equivalent with full PV organizational accountability.

30+ days ago

Drug Safety Associate ProStaff Solutions

Princeton, New Jersey

Safety Data Exchange Agreement (SDEA) Management Act as drug safety representative for SDEAs, collaborate internal and external stakeholders, maintaining oversight of PV obligations outlined within SDEA. Hybrid (3 days onsite/2 days remote) Contract Pay rate: DoE Key Responsibilities Pharmacovigilance Operations Oversee external vendors responsible for case intake and medical information.

30+ days ago

Drug Safety Physician Systimmune

Princeton, NJ

Full time

This individual will also support the clinical R&D team in the oversight of PV service vendors and partners and will need to maintain medical knowledge, as well as current knowledge of drug safety and pharmacovigilance regulations, pharmacovigilance practices, safety surveillance and risk-management practices. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs).

30+ days ago

Drug Safety Physician Systimmune Inc

Princeton, NJ

$150,000–$250,000 / year

30+ days ago

Drug Safety Physician SystImmune, Inc.

Princeton, NJ

$150,000–$250,000 / year

30+ days ago

Drug Safety Contractor ProStaff Solutions

Princeton, New Jersey

Hybrid (3 days onsite/2 days remote) Contract Pay rate: DoE Key Responsibilities Receipt and Handling of emails, letters and faxes related to Adverse Drug Experiences (ADEs) Medical Inquiries (MIs) and Product Quality Complaints (PQCs). The ideal candidate will have hands-on experience in pharmacovigilance, strong organizational skills, and the ability to effectively collaborate with cross-functional stakeholders in a regulated environment.

3 days ago

Remote Pharmacovigilance / Drug Safety Pharmacist Pharmacy Careers

Newark, New Jersey

Remote

Remote Pharmacovigilance Pharmacist – Drug Safety From Home | No Prior Pharma Experience Required Contribute to global patient safety by collecting, evaluating, and documenting adverse events — entirely from home. This role is open to pharmacists from hospital, ambulatory, community, or managed care backgrounds who have strong attention to detail and want to enter the pharmaceutical industry.

18 days ago

Postdoc - Drug Discovery Development and Application Scientist Rutgers The State University of New Jersey

New Brunswick, NJ

Under Policy 100.3.1 Immunization Policy for Covered Individuals, if employment will commence during Flu Season, Rutgers University may require certain prospective employees to provide proof that they are vaccinated against Seasonal Influenza for the current Flu Season, unless the University has granted the individual a medical or religious exemption. The Laboratory for Biomolecular Simulation Research ( http://lbsr.rutgers.edu ) and Institute for Quantitative Biomedicine ( https://iqb.rutgers.edu/ ) at Rutgers, the State University of New Jersey, is in search of a postdoctoral-level drug discovery application scientist.

30+ days ago

Contractor, Drug Metabolism and Pharmacokinetics (DMPK) PTC Therapeutics Inc

Bridgewater, NJ

$45–$70 / hour

A Master's degree in Biology, Chemistry, Biochemistry, Pharmaceutical Science, Pharmacology or other related scientific discipline and a minimum of 2 years of relevant and progressively responsible experience in a pharmaceutical, biotechnology or similar environment OR a Bachelor's degree in these same disciplines and a minimum of 4 years of the same experience. Demonstrated experience in conducting in vitro and in vivo DMPK studies, such as metabolic stability in liver microsomes and hepatocytes, CYP inhibition and induction, and bioanalysis in various matrices etc.

19 days ago

Contractor, Drug Metabolism And Pharmacokinetics (Dmpk) PTC Therapeutics

Bridgewater, NJ

$45–$70 / hour

19 days ago

Certified Alcohol & Drug Counselor - Per Diem |Behavioral Health Services - Evergreen |24365 Bergen New Bridge Medical Center

Paramus, New Jersey

Completion of 270 hours of alcohol and drug education, approved by member boards of the International Certification Reciprocity Consortium (IC&RC) [APCBNJ in New Jersey or its successor], or a regionally accredited college or university which shall be related to the knowledge and skill associated with the functions of an alcohol and drug counselor. Performs all duties with respect, dignity, and impunity according to the ethics of the hospital, adductions field and training, NJ state laws and acts as an advocate for the patients within NBMC, with other facilities establishing positive working relationships within the hospital and the broader community.

30+ days ago

Director, Product Lead, Clinical Safety & Pharmacovigilance (CSPV) Otsuka

Princeton, New Jersey

The Director, Clinical Safety and Pharmacovigilance (CSPV), provides oversight of the safety profile of assigned Otsuka products (both drugs and devices, post market products and clinical development programs) through monitoring safety data, conducting risk analysis, and monitoring adverse events according to GCP and regulatory guidelines, in order to protect the safety of the patients and consumers and the company from legal implications. Key activities include medical analysis and decision making for the development and maintenance of the Company Core Safety Information, ad hoc aggregate safety reports, periodic safety update reports (PSURs), signal detection activities, risk management plan (RMPs/REMS) and individual case safety reports, with proactive engagement in early-stage clinical trial design and safety monitoring.

30+ days ago

Senior Medical Director - Medical Safety Evaluation Mitsubishi Tanabe Pharma

Jersey City, NJ

Provides primary liaison between global/local groups and external groups (Drug Safety Monitoring Boards, regulatory agencies, physician communities, and CROs) on product safety related issues as assigned. Works with medical affairs team to build awareness of the safety of company products in the medical community, including supporting company sponsored Advisory Boards, participating in medical symposia, publishing, attending media events, and other activities.

30+ days ago

Assoc Business Development Director - Safety Solutions IQVIA Holdings Inc

Parsippany, NJ

$89,900–$250,400 / year

Responsibilities include full cycle sales including: target identification, securing and managing client meetings, listening and understanding client needs, addressing client concerns/objections, managing Subject Matter Experts in defining opportunities, proposing solutions, negotiating, obtaining SOWs and closing the deal. The Associate Business Development Director works collaboratively with other colleagues to increase sales of IQVIA's Safety and Regulatory services and technology within the life sciences industry.

30+ days ago

Senior Medical Safety Scientist Acadia Pharmaceuticals Inc

Princeton, NJ

$145,000–$181,700 / year

We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. Support audits, inspections, and regulatory authority inspections by ensuring safety documentation is accurate, complete, and inspection ready while maintaining compliance with global pharmacovigilance regulations and Good Pharmacovigilance Practices (GVP).

26 days ago

Associate Director, Patient Safety Scientist Bristol-Myers Squibb Co

Madison, NJ

$150,300–$182,125 / year

Responsible 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). 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.

18 days ago

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Drug Safety Jobs in Somerville, NJ

Senior Director Clinical Safety MD Daiichi Sankyo, Inc.

Senior Director, Clinical Safety MD Daiichi Sankyo, Inc.

Associate Director, Global Drug Safety & Pharmacovigilance Scientist Genmab AS

Director, Global Drug Safety & Pharmacovigilance Physician Genmab AS

Vice President and Global Head of Drug Safety and Pharmacovigilance Insmed Inc

Drug Safety Associate ProStaff Solutions

Drug Safety Physician Systimmune

Drug Safety Physician Systimmune Inc

Drug Safety Physician SystImmune, Inc.

Drug Safety Contractor ProStaff Solutions

Remote Pharmacovigilance / Drug Safety Pharmacist Pharmacy Careers

Postdoc - Drug Discovery Development and Application Scientist Rutgers The State University of New Jersey

Contractor, Drug Metabolism and Pharmacokinetics (DMPK) PTC Therapeutics Inc

Contractor, Drug Metabolism And Pharmacokinetics (Dmpk) PTC Therapeutics

Certified Alcohol & Drug Counselor - Per Diem |Behavioral Health Services - Evergreen |24365 Bergen New Bridge Medical Center

Director, Product Lead, Clinical Safety & Pharmacovigilance (CSPV) Otsuka

Senior Medical Director - Medical Safety Evaluation Mitsubishi Tanabe Pharma

Assoc Business Development Director - Safety Solutions IQVIA Holdings Inc

Senior Medical Safety Scientist Acadia Pharmaceuticals Inc

Associate Director, Patient Safety Scientist Bristol-Myers Squibb Co

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