62 Results for

Drug Safety Jobs in Jefferson, NJ

Jobs

Basking Ridge, NJ

$226,275–$377,125 / year
Full time

p style="margin:0in;line-height:normal;font-size:12pt;font-family:'aptos' , sans-serif">Download Our Benefits Summary PDF. As a member of SLT/SMT, the role will provide oversight of manufacturing sites according to the product lifecycle, collaborate with Quality teams to complete PPQ planning and the transition to commercial manufacturing activities for the product portfolio, and provide technical expertise to their team of MSMQs.

7 days ago

Basking Ridge, NJ

$280,350–$467,250 / 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.

30+ days ago

Basking Ridge, NJ

$242,700–$404,500 / 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.

30+ days ago

Basking Ridge, NJ

$184,240–$276,360 / year
Full time

p style="margin:0in;line-height:normal;font-size:12pt;font-family:'aptos' , sans-serif">Download Our Benefits Summary PDF. The role will participate in other PV QA projects, tasks, and initiatives as needed and as instructed, including but not limited to including planning and PV QA executing the Pharmacovigilance Quality Strategy Plan in alignment with the DSI business objectives, review of key REMS documents, Health Authority Commitments, Quality Event management, escalation process and the CAPA oversight across applicable functional areas.

Today

$275,000–$350,000 / year

Overseeing and ensure consistent conduct and timely execution of Benefit-Risk activities including pre-marketing risk assessment planning for First-In-Human FIH studies and additional clinical studies in various phases of development safety content of key Modules SCS CLO Labelling in regulatory authority submissions for approval including planning content and execution of Risk Management Plans RMPs and/or Risk Evaluation and Mitigation Strategies REMS for and post-marketing requirements. Our intimate knowledge of muscle biology and biophysics along with our ability to identify and design muscle specific precision small molecules have enabled us to rapidly advance our skeletal muscle and cardiac muscle product candidates into the clinic while also building a robust pre-clinical pipeline.

30+ days ago

$250,000–$289,000 / year

ul>

The primary responsibilities are to manage safety contract service organizations (CSOs) with >=95% compliance with clinical and postmarket safety regulations (including to the FDA, EMA, MHRA, and all assigned international RAs), processes, PV agreements, and database management.

Expertise with clinical trial and post market safety database use, management, and change control (Argus, ArisG, and/or VeevaSafety) and Microsoft Office Suite required (Word, Excel, PowerPoint, Project, Outlook).

13 days ago

li>Partner closely and effectively with the TASH, the Head of Global Safety Strategy and Risk Minimization (GSSRM), the Chief Safety Officer (CSO), the Chief Medical Officer (CMO) JJ IM, the Qualified Person for Pharmacovigilance (QPPV) JJ IM, other JJ IM R&D leaders and the other groups within GMS to proactively assess, respond and communicate safety concerns for products throughout the lifecycle.

The Product Safety Head will help ensure proactive and timely assessments of safety data, understanding of the emerging and known safety profiles of products within the assigned product, preparation of aggregate safety reports and responses to Health Authorities (HA) and, when appropriate, communication of potential and known risks to Senior Management, HAs, Prescribers and/or Patients.

12 days ago

Morristown, NJ

$232,500–$335,833.33 / year

The GPH will collaborate with the Principal Clinical Lead (PCL) and Global Project Manager (GPM) to lead the cross-functional GPT (which includes translational, regulatory, drug manufacturing, safety, medical and commercial compound leads), to ensure correct planning and implementation of end-to-end compound strategy. Key Responsibilities: The Global Project Head (GPH) drives worldwide clinical development and life cycle management for a late-stage Sanofi Antibody Drug Conjugate (ADC) compound within Solid Tumor Oncology.

30+ days ago

Rahway, NJ

Remote

$190,800–$300,300 / year

p>Reporting to the Director of Device Regulatory Affairs for Autoinjector Development Programs, the Director/Principal Scientist in Devices and Drug-Device Combinations CMC is responsible to support Device CMC regulatory activities for Our Company's autoinjector, inhalation, and other delivery system products in accordance with global regulations and guidelines and is responsible for technical content input and coordination of CMC submissions for all assigned activities.

Primary responsibilities include, but are not limited to:

Responsibilities:

Lead Device Regulatory Affairs strategies for autoinjector, inhalation, and other delivery system development programs by ensuring robust assessment of scientific content and critical evaluation of supporting regulatory documentation to confirm acceptability and identification of potential risks.

30+ days ago

$115,000–$130,000 / year

Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialized clinical diagnostics testing.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable.

30+ days ago

$255,000–$302,000 / year

Director will set direction and deliver applied AI/ML solutions across internal workflows and externally facing outputs, ranging from R&D insights to partner-ready analyses, while partnering closely with scientific teams and, when needed, external vendors/partners to solve real problems. It requires a leader who can build, validate, and operationalize models using real-world biopharma data, raise the signal-to-noise ratio in small or unstructured datasets, and include synthetic control arm approaches where appropriate.

30+ days ago

Paramus, New Jersey

p>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

Madison, NJ

$217,520–$263,577 / 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.

30+ days ago

Remote

$247,000–$337,000 / year

p>For New York City Residents:

To assist in identifying candidates with qualifications matching those required and/or preferred for this role, Insmed uses an Automated Employment Decision Tool ("AEDT") that employs artificial intelligence to analyze and score information provided in resumes and application materials including, but not limited to, skills, work experience, education, and job-related qualifications.

Work with the DSPV leadership to develop the strategy and implementation of safety and benefit-risk management for assigned products; develop key content of Risk Management documents (RMPs, REMS) for assigned products.

30+ days ago

Nutley, NJ

Remote

The individual will verify the accuracy and completeness of information for each adverse event report for which he/she is assigned in conjunction with the source documents and ensure that all activities are performed in a manner consistent with SOPs. Code and enter information into the Product Safety database for Adverse Events reported in association with ***’s Marketed and investigational products.

30+ days ago

Nutley, NJ

Remote

strong>Description of Responsibilities:

Code and enter information into the Product Safety database for Adverse Events reported in association with client’s Marketed and investigational products.
The individual will be responsible for verifying the accuracy and completeness of information for each adverse event report for which he/she is assigned in conjunction with the source documents and ensuring that the activities are performed in a manner consistent with SOPs.

30+ days ago

East Hanover, NJ
$204,000–$379,000 / year
Coordinate with Global Countries and Regions for simplified/harmonized practices and case exchange and collaborate with Regulatory Affairs, Quality, Legal/Data Privacy, Risk Management, and Medical Safety to support submissions, inspections, signal detection, RMPs, REMS, labeling updates, and periodic reports. Key Responsibilities:Strategic & Operational LeadershipLead end-to-end case management operations, including case intake, triage, processing, follow‑up, quality control, case corrections and submission ensuring timely, accurate, and compliant safety reporting.
26 days ago

Morristown, NJ
$178,500–$297,500 / year
li>
Review, preparation, contribution and/or approval of clinical development documents including clinical development plans, SAPs, study protocols, investigator brochures, data monitoring plans, study reports, integrated summary of safety, summary of clinical safety, and labeling. But progress doesnt happen without people people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen.
30+ days ago

Nutley, NJ
Remote
$25
Computer proficiency required, including data entry of adverse event information. Description of Responsibilities: Code and enter information into the Product Safety database for Adverse Events.
30+ days ago

NJ
$286,560–$347,244 / year
li>
Oversee, prepare and/or review aggregate safety review documents (eg, Development Safety Update Reports [DSUR], Periodic Benefit-Risk Evaluation Reports [PBRER]) and safety sections of relevant clinical trial documents (eg, protocols, clinical study reports [CSR], investigator brochures [IB], informed consent forms [ICF]) and regulatory filings (eg, clinical trial applications [CTA], marketing authorization applications [MAA]).
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.
30+ days ago

NJ
$137,000–$235,750 / year
The Company may however extend this time-period, in which case the posting will remain available on https://www.careers.jnj.com to accept additional applications.
Function with a high level of independence, with minimal guidance from the Director, Safety Analysis Scientist (SAS) Therapeutic Area Lead (TAL), be able to link discussions to content, and consistently deliver high quality results with minimal guidance.
30+ days ago

Nutley, NJ
Remote
$23–$26 / hour
The individual will be responsible for verifying the accuracy and completeness of information for each adverse event report for which he/she is assigned in conjunction with the source documents and ensuring that the activities are performed in a manner consistent with SOPs. Code and enter information into the Product Safety database for Adverse Events reported in association with *** s Marketed and investigational products.
30+ days ago

NY
Remote
$119,700–$222,300 / year
May be PCS part-time PTMEssential Requirements:• PhD or MVSc/MS/M.Pharm with 7+ years of experiences in drug discovery and/or development, preferably as Study Director or Study Monitor in the early preclinical screening and GLP studies• In-depth knowledge of toxicology assays in early development, Safety pharmacology and genotoxicity• Proficient with full range of techniques used in job and core areas. The Study Monitor is appointed to each outsourced preclinical study based on relevant technical expertise, designated disease area and/or scientific background knowledge and acts as the primary scientific contact for the Study Director at the Contract Research Organization (CRO).The Study Monitor is responsible for overseeing the progress of the study and for ensuring that the study is conducted, recorded and reported according to the study protocol.
11 days ago

NY
$185,369–$308,948 / year
o The current base salary range for this position is expected to be between $185,369 and $308,948 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators.
Proactively assesses and evaluates the clinical implications of safety data from all sources in order to understand and communicate the benefit-risk profile of assigned drugs in development and in the post-marketing settings as appropriate.
30+ days ago

Warren, NJ
$156,313–$214,930 / year
Define safety strategy and provide expert safety input to R&D innovation projects for all CH product types (e.g., medicines, medical devices, cosmetics, dietary supplements, digital health projects) within assigned therapeutic category and/or business unit and represent safety function on project teams and other relevant cross-functional forums. In line with a risk-proportionate framework for product vigilance, the Associate Director, Consumer Safety Science is accountable for defining and developing the safety strategy for R&D innovation projects, as well as maintenance of business activities for medium to high-risk products.
30+ days ago

New
NY
$285,800–$365,800 / year
This includes but not limited to safety strategies and plans; Target Early Profile (TEP)/Target Product Profile (TPP), safety Revised 10 JUNE 2026 content of protocols; Investigator's Brochure; Informed Consent Form; Safety Analysis Plan; clinical study reports; CCDS/product labels; Risk Management Plans; Summary of Clinical Safety and ISS; aggregate safety reports; Health Authority Request for Information/Queries; relevant safety communications (e.g., DIL/DHPC/DHCP letter), and scientific publications.
Accountable for safety data content and provide strategic insights and medical leadership to Data Monitoring Committees (DMC)/Safety Monitoring Committees Revised 10 JUNE 2026 (SMC), including input on charters and participation in meetings as required across all molecules/programs within the franchise.
4 days ago

$292,000–$401,500 / year
argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to treat patients across dozens of severe autoimmune diseases. The role also requires close collaboration with internal stakeholders such as Regulatory Affairs, Clinical Development, and Medical Affairs, as well as external partners including key opinion leaders and regulatory agencies, to align safety communications and ensure the safe and effective use of argenx products.
30+ days ago

Nutley, NJ
Remote
$28.57
Preliminary evaluation of clinical trial, spontaneous (post-marketing), and solicited reports of adverse events, including communication with partners and affiliates when necessary to verify completeness and accuracy. Receipt and triage of adverse event reports for marketed and investigational products from all sources.
30+ days ago

New
NY
$118,700–$194,400 / year
p>We are seeking a highly experienced sales and business development professional to drive growth across Commercial, Real-World Evidence (RWE), Clinical, Regulatory, and Safety research services within pharmaceutical and biotechnology organizations.
Oracle maintains broad salary ranges for its roles in order to account for variations in knowledge, skills, experience, market conditions and locations, as well as reflect Oracle''s differing products, industries and lines of business.
2 days ago

NY
$146,300–$306,400 / year
Develop longitudinal relationships with key client executives and drive discussions concerning strategy, structure, management and operations to support enterprise-wide leadership, and safety/quality teams to ensure that organizational wide safety and quality goals and objectives and risk reduction strategies are implemented effectively wherever appropriate while engaging stakeholders in the process.
At least 7 years total combined higher education and related work experience, including:
At least 2 years licensed health care practice, clinical consulting and/or other clinical healthcare information technology (HCIT) work experience.
13 days ago

New
East Hanover
li>Provide expert safety input to the clinical development program for assigned projects/products and be an active member of the Global Program Team (GPT), Global Clinical Team (GCT) and Clinical Trial Team (CTT) -Is responsible for safety issue management from formation of Global Program Team (GPT) through Life Cycle Management. As Senior Global Program Safety Team Lead, you will bring clinical insight, strategic thinking, and strong leadership to complex safety decisions, helping shape development pathways and advance medicines that could change patients’ lives.
.
1 day ago

Morristown, NJ
$178,500–$297,500 / year
But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.
30+ days ago

Elizabeth, New Jersey
UofL Health is a fully integrated regional academic health system with five hospitals, four medical centers, nearly 200 physician practice locations, more than 700 providers, the Frazier Rehab Institute and Brown Cancer Center. With more than 12,000 team members—physicians, surgeons, nurses, pharmacists, and other highly skilled health care professionals—UofL Health is focused on one mission: delivering patient-centered care to each and every patient each and every day.
Job Description: .
12 days ago

Morristown, NJ
$178,500–$257,833.33 / year
These activities entail formulating the nonclinical safety strategies, designing safety pharmacology and toxicology studies, authoring regulatory documents, being a member of an integrated Project Team, interacting with internal and external partners, and interacting with and responding to global regulatory agencies.
Our Team:
The candidate will be part of a dynamic interactive Preclinical Safety group that spans all aspects of the drug development value chain providing toxicology and safety pharmacology expertise as a member of global project teams.
12 days ago

New
NY
$133,000–$212,000 / year
This role makes harm severity and IMDRF coding determinations and drives continuous improvement initiatives in post market surveillance activities, collaborating with technical experts to resolve issues and support corrective actions.
The Medical Safety Manager, Complaints Handling, performs clinical assessments on complaints related to harm to assist in regulatory reportability determination and serves as the primary clinical liaison between Post Market Surveillance and Medical Safety, facilitating escalations as necessary.
6 days ago

Paramus, NJ
$300,000–$350,000 / year
We are consistently ranked by U.S. News & World Reports Best Hospitals, receiving high "Honor Roll" status, and are highly ranked: No. 1 in Geriatrics, top 5 in Cardiology/Heart Surgery, and top 20 in Diabetes/Endocrinology, Gastroenterology/GI Surgery, Neurology/Neurosurgery, Orthopedics, Pulmonology/Lung Surgery, Rehabilitation, and Urology. Mount Sinai advances health for all people, everywhere, by taking on the most complex health care challenges of our time - discovering and applying new scientific learning and knowledge; developing safer, more effective treatments; educating the next generation of medical leaders and innovators; and supporting local communities by delivering high-quality care to all who need it.
30+ days ago

NY
$81,700–$166,100 / year
p>The ideal candidate is a healthcare technology and consulting leader who excels in complex environments, builds strong relationships, drives accountability, and delivers measurable results while balancing multiple priorities and stakeholders. This individual will act as a trusted advisor to both internal and external stakeholders, lead complex engagement efforts, manage project portfolios, and continuously refine the QPS engagement methodology to support successful outcomes across the VA enterprise.
13 days ago

New
NY
$68,800–$133,700 / year
ul>
Actively works to promote operational excellence by monitoring and improving processes related to management of Individual Case Safety Reports (ICSRs) (including Adverse Events, Serious Adverse Events and Device Deficiencies/Events), Clinical Events Committees (CECs), and Data Monitoring Committees (DMCs). Gathers member documents, develops member contracts, schedules and moderates meetings, and ensuring action items/minutes are completed and properly documented.
4 days ago

New
Wayne, NJ
Remote
The CMO plays a critical role in building a strong, flexible, and capable direct as well as virtual organization, supporting new product and especially fielded product safety across the enterprise, leading Medical Education and any other shared medical services that might be added in the future, serving as the medical and safety director for Surgical Workflows, and serving as a key voice of the clinician and patient within the company.
The Corporate Medical and Chief Safety Officer (CMCSO) leads the Corporate Medical function at Getinge, responsible for developing and leading the company-wide Safety function and processes, serving as the Medical & Safety Director for Surgical Workflows, and leading the Medical Education group.
4 days ago

NY
$285,000–$330,000 / year
p>Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Additionally, you will play a key role in supporting drug safety and pharmacovigilance activities to ensure high-quality data generation to support the safety and efficacy of our products in development.
28 days ago

NJ
Remote
$133,000–$173,000 / year
p>For New York City Residents:
To assist in identifying candidates with qualifications matching those required and/or preferred for this role, Insmed uses an Automated Employment Decision Tool ("AEDT") that employs artificial intelligence to analyze and score information provided in resumes and application materials including, but not limited to, skills, work experience, education, and job-related qualifications. Reporting to the Senior Director, DSPV Operational Excellence and Compliance, you'll be responsible for the end-to-end development, implementation, and lifecycle management of Safety Data Exchange Agreements (SDEAs), Pharmacovigilance Agreements (PVAs), and Pharmacovigilance Clauses (PVCs).
30+ days ago

NJ
$70,000–$95,000 / year
li>Determine and perform appropriate case follow-up activities including generation of follow-up requests via fax, phone, mail, or e-mail and product complaint notifications to consumers, HCPs, Specialty Pharmacies and/or vendors.
Pharming takes into consideration a combination of candidate's work experience, training, and education, as well as the scope of the role, complexity, and external market and internal value when determining a salary level.
30+ days ago

$192,000–$264,000 / year
argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to treat patients across dozens of severe autoimmune diseases.
Demonstrated experience using digital tools and automation to improve efficiency, visibility, and oversight across regional pharmacovigilance activitiesExcellent oral and written communication skills.
25 days ago

Bridgewater, NJ
Remote
$46.67–$48 / hour
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. The associate will train trial personnel and relevant Safety Surveillance staff on processes, participate in the design and implementation of safety reporting databases, and coordinate safety reporting across multiple trials.
24 days ago

Morristown, NJ
$178,500–$257,833.33 / year
p>Experience / Skills:
MD or MD/PhD in a relevant scientific discipline, preferably pulmonology, with at least 2 years relevant experience in clinical development within the pharmaceutical industry, academia, or government agencies such as the NIH, FDA, or other equivalent national or international public health and regulatory organization.
On Clinical Development, the CRD:
Designs the global clinical development strategy (in close cooperation with other members of the team, particularly Regulatory Affairs end Health Economics) and leads the clinical development with regard to ongoing development activities and planned LCM for labelling changes.
30+ days ago

Jersey City, NJ
p>The Clinical Development Executive Medical Director is the clinical leader of the specific clinical programs assigned with responsibility for outlining the overall clinical development strategy in line with regulatory requirements and sound scientific rationale, designing the clinical protocols, guiding the Clinical Operations team towards the adequate implementation of such protocols, ensuring adequate medical monitoring activities are implemented for the conduction of clinical studies and analyzing the data from the clinical program. The individual will also be responsible for ensuring adequate implementation of the global safety surveillance and pharmacovigilance for the investigational products, including review and analysis of safety data from clinical trials and other permitted sources (e.g., early access/expanded access programs, if applicable), identification and investigation of safety signals, and management of the benefit-risk profile for assigned compounds.
30+ days ago

NY
$170,000–$215,000 / year
Sionna's goal is to deliver differentiated medicines for people living with CF that can restore their CFTR function to as close to normal as possible by directly stabilizing CFTR's nucleotide-binding domain 1 (NBD1), which the company believes is central to potentially unlocking meaningful improvements in clinical outcomes and quality of life for people with CF. The AD PV Scientist will lead or contribute to key PV deliverables and activities associated with signal detection and management, benefit-risk evaluations and regulatory and aggregate safety reporting processes, PV SOP development and management, and oversight of the PV vendor and Clinical CRO safety activities.
30+ days ago

NY
Remote
$72,000–$100,000 / year
Assess ICSRs for individual adverse event terms signifying seriousness and expectedness relative to the product label while also referencing guidance documents provided by regulatory authorities on assessing seriousness. At least 2 years experience working in Pharmacovigilance, a Contract Research Organization (CRO) or other related scientific area; with specific experience working with Medical Devices, preferred.
30+ days ago

Jersey City, NJ
$270,000–$294,500 / year
p>In partnership with your Manager:
• Design and conduct early-stage or late-stage clinical development trials as needed, including, but not limited to assessing clinical safety and efficacy data, performing medical monitoring, and be responsible for other study-related clinical activities.
This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in our New Jersey offices to ensure effective collaboration and high-quality execution of your clinical work.
30+ days ago

NY
$175,000–$215,000 / year
p>Hansa Biopharma is a fast-growing, commercial-stage biopharmaceutical company, pioneering the development and commercialization of innovative, lifesaving and life altering treatments for patients with acute or complex immune disorders.
Our broad therapeutic pipeline based on the company's proprietary IgG-cleaving enzyme technology platform has potential to address serious unmet medical needs in autoimmune diseases, gene therapy, and transplantation.
13 days ago

Resume Resources

Free Resume Templates Free Resume Builder

Get noticed by top employers!

Upload your resume to let employers know you're open to Drug Safety job opportunities. Plus, receive relevant job recommendations in your inbox.

Create A Free Account

Drug Safety Jobs in Jefferson, NJ

Job Description.

Job Description: .

Resume Resources

Similar Job Searches

Get noticed by top employers!

Drug Safety Jobs in Jefferson, NJ

Head of Quality Assurance, Drug Product, GMP QA Daiichi Sankyo, Inc.

Senior Director, Clinical Safety MD Daiichi Sankyo, Inc.

Job Description.

Senior Director, Clinical Safety Scientist Daiichi Sankyo, Inc.

Director, PV QA DSI Daiichi Sankyo, Inc.

Executive Director, Drug Safety & Pharmacovigilance (EDG-2026015) Edgewise Therapeutics Inc

Senior Director, Drug Safety and Pharmacovigilance BridgeBio Pharma Inc

Sr Director Product Safety Head - Cellular Therapy, Hematology Johnson & Johnson

Global Project Head, Solid Tumor Antibody Drug Conjugates (ADCs) Sanofi

Director, Drug & Device Combo (Autoinjector/Inhalation) Reg.-CMC (Remote) Merck & Co Inc

Business Development Manager - Drug Discovery Eurofins Scientific SE

Senior Director AI and Data Science Drug Discovery and R&D Enablement Lexeo Therapeutics Inc

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

Director, Patient Safety Scientist Bristol-Myers Squibb Co

Director, Medical Safety Lead - DSPV, Gene Therapy Insmed Inc

Product Safety Data Coordinator and Coding Associate Lenmar Consulting, Inc.

Product Safety Data Coordinator and Coding Associate Integrated Resources, Inc

Head of US Patient Safety Pharmacovigilance Case Management Novartis AG

Global Safety Officer, I&I Sanofi

Product Safety Data Coordinator and Coding Associate Lancesoft

Director, Medical Safety Assessment Physician Bristol-Myers Squibb Co

Associate Director, Safety Analysis Scientist Johnson & Johnson

Product Safety Data Coordinator and Coding Associate Artech LLC

Study Monitor-Principal Scientist, Translational Medicine/Preclinical Safety (PCS) Remote Position Novartis AG

Associate Director, Global Safety Lead Agios Pharmaceuticals Inc

Associate Director, Consumer Safety Science Haleon Plc

Executive Director, Safety Franchise Area Lead BeOne Medicines AG

Medical Safety Lead Argenx SE

Product Safety Coordinator Lancesoft

Senior Client Partner - Commercial, Real-World Evidence, Clinical, Regulatory & Safety Oracle Corp

Lead Clinical Quality and Patient Safety Healthcare Executive Oracle Corp

Sr. Global Program Safety Team Lead - Oncology Novartis

Global Safety Officer Sanofi

Healthcare Safety and Security Officer, Mary and Elizabeth Hospital, 6p-6a UofL Health

Job Description: .

Distinguished Scientist, Safety Assessment Project Expert Sanofi

Medical Safety Manager Complaints Handling Philips

Patient Safety Officer (PSO) and Associate Medical Director, Hospitalist Services - Physician - Valley Health System - New Jersey Mount Sinai Health System

Senior Engagement Owner - Quality and Patient Safety Oracle Corp

Senior Safety Associate NAMSA Inc

Corporate Medical & Chief Safety Officer (USA Remote) Getinge AB

Medical Director Pharmacovigilance Apogee Therapeutics Inc

Manager, DSPV Pharmacovigilance Agreements Insmed Inc

Associate, Global Pharmacovigilance Pharming Group NV

Regional Pharmacovigilance Lead (US) Argenx SE

Pharmacovigilance Associate Actalent Inc

Clinical Research Director - Rare Diseases Sanofi

Executive Medical Director, Clinical Development - M.D. (Nephrology) Clinical Dynamix, Inc.

Associate Director, Pharmacovigilance Scientist Sionna Therapeutics Inc

Pharmacovigilance Specialist-Registered Nurse Safetycall International LLC

Senior Director, Clinical Research Eikon Therapeutics Inc

Sr. Manager/Associate Director, Pharmacovigilance Hansa Biopharma AB

Resume Resources

Similar Job Searches