37 Results for

Drug Safety Jobs in Roosevelt Island, NY

Jobs

Associate Director, Global Safety Lead - Remote Agios Pharmaceuticals

New York, NY

Remote

$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.

18 days ago

Associate Director, Medical Review Lead, MSRM - Remote Agios Pharmaceuticals

New York, NY

Remote

$185,369–$308,948 / year

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. This role provides oversight of medical review for Individual Case Safety Reports (ICSRs) across investigational and marketed products, ensuring medical accuracy, regulatory compliance, and high-quality safety data to support pharmacovigilance and risk management activities.

18 days ago

Vice President, Drug Safety and Pharmacovigilance DSPV Immunovant Inc

New York, NY

$400,000–$425,000 / year

Medical expert accountable for overall DSPV strategy and all deliverables of the DSPV function, including responsibilities for pharmacovigilance-related documents (e.g., DSUR) as well as safety sections of key documents (e.g., IBs, RSI, ICFs, study protocols, CSRs) and other applicable activities (IND/CTA, requests for information, regulatory responses). Responsible for oversight of the DSPV department, including building and managing a team of DSPV professionals (operations and safety science) to execute the development strategy and support registrational/post-marketing activities in a compliant and collaborative environment, in accordance with long-term strategic goals.

30+ days ago

Senior Director, Drug Safety and Pharmacovigilance BridgeBio Pharma Inc

$222,300–$255,000 / year

Configure and administer the Veeva Safety platform (Vault Safety Suite: Safety, SafetyDocs, Signal, Workbench), including user administration, workflow routing, coding configurations (MedDRA, WHO Drug), and business rules. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience within the industry, educational background, location of residence and performance during the interview process.

30 days ago

Drug Safety Associate III System One

Stamford, Connecticut

Minimum 3 years in Drug Safety Operations role; Experience overseeing CRO teams of case processors preferred. Identify adverse events, seriousness, and listedness/labeledness for case assessment; review additional incoming information to determine reportability.

30+ days ago

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

$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

Business Development Manager - Drug Discovery Eurofins Scientific SE

$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

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, Pharmacovigilance / Product Safety Insmed Inc

Remote

$247,000–$337,000 / year

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. Have leadership of the Safety Review Team(s) for assigned products and development compounds, and responsible for the management of ongoing and cross functional assessment of benefit risk profiles and related actions, including writing and updating of the benefit-risk documents such as Safety Signal Assessment Reports for assigned products and development compounds.

9 days ago

Executive Director, Safety Operations BeOne Medicines AG

$285,800–$365,800 / year

Supervisory Responsibilities: As Function head, leads GPS Safety Operations Team: Global ICSR Management, Global ICSR Submission, Trial Safety Operations, China Post Marketing Safety Operations, Safety Systems and Supporting. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location.

7 days ago

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

Remote

$247,000–$337,000 / year

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.

10 days ago

Product Safety Data Coordinator and Coding Associate Artech LLC

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

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

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

Associate Director, Global Safety Lead Agios Pharmaceuticals Inc

$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

Product Safety Data Coordinator and Coding Associate Integrated Resources, Inc

Nutley, NJ

Remote

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. 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.

30+ days ago

Product Safety Data Coordinator and Coding Associate Lancesoft

Nutley, NJ

Remote

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

Executive Director, Safety Franchise Area Lead BeOne Medicines AG

$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.

21 days ago

Director, Global Patient Safety Sciences - General Medicine Regeneron Pharmaceuticals Inc

In this role, a typical day might include: • This Director position is directly responsible for all aspects of Global Patient Safety activities for assigned compounds and products in support of safety surveillance, signal management, communication of the safety profile as appropriate for the stage in the asset lifecycle, benefit risk assessment, safety responses to regulatory agency queries, safety documents (DSURs, PSURs, development RMPs, RMPs, etc.) and the review of clinical documents (Investigator Brochures, protocols, clinical study reports, etc.). • Represent Global Patient Safety for assigned compounds on cross-functional teams, including Regenerons Safety Oversight Committee (RSOC), Independent Data Monitoring Committees (IDMC), Strategic Program Team (SPT) and other teams with members external to Regeneron (alliance partners, CROs).

30+ days ago

Product Safety Coordinator Lancesoft

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

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

$118,700–$194,400 / year

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.

19 days ago

Senior Manager, Global Patient Safety - General Medicine Regeneron Pharmaceuticals Inc

Tarrytown, NY

$150,500–$245,500 / year

We may ask you to represent GPS on cross-functional teams, including Regeneron Safety Oversight Committee (RSOC), Independent Data Monitoring Committees (IDMC) and other teams with members external to Regeneron. The Senior Manager of Global Patient Safety (GPS) will play a key scientific role in safety strategies for molecules in clinical development and post-marketing phases in the assigned Therapeutic Area.

30+ days ago

Safety, Health & Environmental Manager Manpower

Ronkonkoma, NY

$50.48–$52.88 / hour

ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2023 ManpowerGroup was named one of the World's Most Ethical Companies for the 14th year - all confirming our position as the brand of choice for in-demand talent.

22 days ago

Director of Regulatory and Patient Safety Stony Brook University

Stony Brook, NY

$142,800–$203,597 / year

2602444'',''2602444'',''TH Senior Staff Associate'',''TH Senior Staff Associate'',''Clinical Management'',''Clinical Management'',''US-NY-Stony Brook'',''US-NY-Stony Brook'',''JC Continued Readiness'',''JC Continued Readiness'',''Full-time'',''Full-time'',''Day Shift'',''Day Shift'',''8:30-5'',''8:30-5'',''Sat, Sun'',''Sat, Sun'',''Jul 2, 2026'',''Jul 2, 2026'',''Oct 1, 2026, 3:59:00 AM'',''Oct 1, 2026, 3:59:00 AM'',''142800 - 203597'',''142800 - 203597'','''','''',''SL5'',''SL5'',''Stony Brook University Hospital'',''Stony Brook University Hospital'',''false'',''736662'',''736662'',''true'',''736662'',''false'',''Submission for the position: Director of Regulatory and Patient Safety - (Job Number: 2602444)'',''false'',''736662'',''false'',''true''. The department will utilize the Director''s expertise to help prioritize projects, to develop detailed project plans for major safety & regulatory initiatives, assist other members of the department in planning projects, and assure a structured, well-planned approach for successful outcomes & project completion.

14 days ago

Associate Director, Pharmacovigilance/ Product Safety Insmed Inc

Remote

$179,000–$232,500 / year

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. Author, review and provide input and approval for drug-safety related regulatory reports and clinical study documents including clinical study protocols, Informed Consent Forms, Investigator Brochures, Integrated Summary of Safety (ISS), Integrated Summary of Efficacy (ISE), MedDRA coding of AEs, product package and labeling.

9 days ago

Public Safety Officer I FT (32 hours) Unarmed Second Shift AMC Grafton Advocate Health and Hospitals Corporation

Port Washington, Washington

Typically requires 1 years of experience in a security, related public safety, or customer service area that includes experiences in responding to emergent situations and identifying and resolving issues that pose a potential risk to patients, visitors, teammates and/or property. Performs routine responsibilities during interior and exterior patrols to ensure safety and security, including but not limited to inspections to identify vulnerabilities, hazards, and fire conditions, audits of Interim Life Safety Measures, patient valuables management, and thorough contraband searches.

15 days ago

Senior Engagement Owner - Quality and Patient Safety Oracle Corp

$81,700–$166,100 / year

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.

30 days ago

Manager, DSPV Pharmacovigilance Agreements Insmed Inc

Remote

$133,000–$173,000 / year

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).

10 days ago

PV Scientist (Senior Director) Nektar Therapeutics

$280,000–$325,000 / year

Director, PV Scientist to range from $280,000 to $325,000 for candidates in the Bay Area and will depend, in part, on successful candidate location and qualifications for the role, including education and experience. This role serves as the safety expert for company products at all stages of development (Phase 1, 2, 3, and post-approval) and actively participates in the oversight of patient safety across all ongoing clinical trials.

7 days ago

Senior Director, Clinical Research Eikon Therapeutics Inc

Jersey City, NJ

$270,000–$294,500 / year

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

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

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

Associate Director, Pharmacovigilance Scientist Sionna Therapeutics Inc

$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

Sr. Manager/Associate Director, Pharmacovigilance Hansa Biopharma AB

$175,000–$215,000 / year

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.

30 days ago

Vice President, Clinical Development Geron Corp

Remote

$385,000–$425,000 / year

The Vice President of Clinical Development is responsible for providing strategic leadership of the overall development and commercialization of one or more hematology/oncology programs, including overarching responsibility for the clinical development strategy. Work effectively with internal and external stakeholders to ensure efficient execution of clinical trial programs, including study design, protocol writing, start up, execution, analysis, and submission to regulatory authorities.

30+ days ago

Subject Matter Expert (Pharmacovigilance Systems) YDTS Global

Jersey City, New Jersey

Should be able to review and provide feedback on work instructions associated with ongoing safety database maintenance projects, including upgrades, Medical Dictionary for Regulatory Activities (MedDRA) / WHO Drug versioning, direct Electronic Submission Gateway (ESG) setup, etc. Our client solutions free up responsible personnel within Pharma companies to execute their stated responsibilities while staying true to the laws of the land, and ultimately achieving a balance between compliance and managing business risks.

16 days ago

Director, Clinical Science Lantheus Holdings Inc

Remote

$191,000–$286,000 / year

Contribute to authoring and lead design/reviews of key product and study-related documents and deliverables, including but not limited to Clinical Protocols and amendments, Investigator Brochures, Study Manuals, Case Report Forms, Informed Consent Forms, Clinical Study Reports, Annual Reports, regulatory submissions, abstracts and publications. Interacts with internal and external stakeholders (Key Opinion Leaders, Medical Director, vendors, committees) in support of clinical trial objectives and deliverables, including investigator-sponsored trials.

3 days ago

Senior PV Scientist Praxis Precision Medicines Inc

$136,000–$156,000 / year

As Praxis advances its pipeline and prepares for regulatory submissions, this position plays a critical role in strengthening U.S.-based pharmacovigilance footprint, enhancing vendor oversight, supporting implementation of evolving safety infrastructure, and ensuring inspection readiness. Collaborate with Clinical Operations, Regulatory, Medical Affairs, Commercial, and Quality to ensure aligned safety processes, including call center setup, partner safety data exchange, and commercialization readiness activities.

15 days ago

Executive Director, Global Clinical Pharmacology & Development Technology Solutions BeOne Medicines Ltd

$267,400–$347,400 / year

They collaborate with other GTS R&D Business Partners to identify risks, interdependencies, and opportunities to inform financial responsibility, robust planning, and reliable execution, and partners with GTS Shared Services & Centers of Excellence (CoEs) to ensure adherence to BeOne's technology architecture, security & compliance, and system and project life cycle governance. At BeOne we believe that access to life-changing medicine sees no borders, and GTS makes this possible by delivering a cloud-based backbone and SaaS systems for efficient delivery, growth, and maintenance, while positioning our staff to demonstrate their domain, technical, and governance expertise as partners of the BeOne global team.

30+ days ago

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Drug Safety Jobs in Roosevelt Island, NY

Associate Director, Global Safety Lead - Remote Agios Pharmaceuticals

Associate Director, Medical Review Lead, MSRM - Remote Agios Pharmaceuticals

Vice President, Drug Safety and Pharmacovigilance DSPV Immunovant Inc

Senior Director, Drug Safety and Pharmacovigilance BridgeBio Pharma Inc

Drug Safety Associate III System One

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

Business Development Manager - Drug Discovery Eurofins Scientific SE

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

Director, Pharmacovigilance / Product Safety Insmed Inc

Executive Director, Safety Operations BeOne Medicines AG

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

Product Safety Data Coordinator and Coding Associate Artech LLC

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

Associate Director, Global Safety Lead Agios Pharmaceuticals Inc

Product Safety Data Coordinator and Coding Associate Integrated Resources, Inc

Product Safety Data Coordinator and Coding Associate Lancesoft

Executive Director, Safety Franchise Area Lead BeOne Medicines AG

Director, Global Patient Safety Sciences - General Medicine Regeneron Pharmaceuticals Inc

Product Safety Coordinator Lancesoft

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

Senior Manager, Global Patient Safety - General Medicine Regeneron Pharmaceuticals Inc

Safety, Health & Environmental Manager Manpower

Director of Regulatory and Patient Safety Stony Brook University

Associate Director, Pharmacovigilance/ Product Safety Insmed Inc

Public Safety Officer I FT (32 hours) Unarmed Second Shift AMC Grafton Advocate Health and Hospitals Corporation

Senior Engagement Owner - Quality and Patient Safety Oracle Corp

Manager, DSPV Pharmacovigilance Agreements Insmed Inc

PV Scientist (Senior Director) Nektar Therapeutics

Senior Director, Clinical Research Eikon Therapeutics Inc

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

Associate Director, Pharmacovigilance Scientist Sionna Therapeutics Inc

Sr. Manager/Associate Director, Pharmacovigilance Hansa Biopharma AB

Vice President, Clinical Development Geron Corp

Subject Matter Expert (Pharmacovigilance Systems) YDTS Global

Director, Clinical Science Lantheus Holdings Inc

Senior PV Scientist Praxis Precision Medicines Inc

Executive Director, Global Clinical Pharmacology & Development Technology Solutions BeOne Medicines Ltd

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