253 matching jobs for “Safety Data Lead I”

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Exact titles rank first, then title variations and keywords in descriptions. These labels aren't qualification scores. Without keywords, recently added jobs appear first.

Merck (MSD)

Safety Data Lead I

CHN - Beijing - Beijing (Wangjing Park)

The Safety Data Lead is responsible for the analysis and interpretation of adverse experience (AE) reports of varying …

Added Oct 16, 2026

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Merck (MSD)

Safety Data Lead I

CHN - Beijing - Beijing (Wangjing Park)

The Safety Data Lead is responsible for the analysis and interpretation of adverse experience (AE) reports of varying …

Added Oct 16, 2026

Save job

Merck (MSD)

Safety Data Lead I

CHN - Beijing - Beijing (Wangjing Park)

The Safety Data Lead is responsible for the analysis and interpretation of adverse experience (AE) reports of varying …

Added Oct 16, 2026

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IQVIA Holdings

… and therefore report program/portfolio level metrics and provide oversight of projects they do not directly lead. • Performs role of solution architect responsible for crafting and defending proposed solutions to new …

Added Oct 15, 2026

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Pfizer

Sr Director, Clinical Excellence Group Lead (I&I)

Cambridge, Massachusetts, United States

Full time
Regular

Pay posted by employer$214,900–$358,100 per year

Team Leadership & Change Management Lead, mentor, and develop a team of high-performing clinical scientists, fostering a culture of collaboration, …

Added Oct 16, 2026

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Bristol-Myers Squibb

Lead Material Operations Specialist I

Leiden – NL

Full time
Temporary

… executing routine activities related to the management, cleansing and movement of all type of materials (i.e. cold chain, ambient) supporting internal and external customers, while following Standard Operating …

Added Oct 15, 2026

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Johnson & Johnson

Medical Safety Officer - PALM

High Wycombe, United Kingdom +4 locations

Full time
Regular

… can influence these through his/her performance. Essential Job Duties and Responsibilities The Medical Safety Officer (MSO) - Post Approval Lifecycle Management (PALM) is a physician with training or experience in …

Added Oct 15, 2026

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Gilead Sciences

Associated Director Data & AI Delivery Lead – Clinical Development

Foster City, California, United States

Full time
Regular

Pay posted by employer$195,670–$253,220

… people ready to make a direct impact. Join Gilead and help create possible, together. Associated Director Data & AI Delivery Lead – Clinical Development As part of the enterprise AI strategy, the Data & AI Delivery …

Added Oct 15, 2026

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Johnson & Johnson

Associate Director, Safety Analysis Scientist

High Wycombe, United Kingdom

Full time
Regular

… the elimination of cancer by discovering new pathways and modalities for finding treatments and cures. We lead where medicine is going and need innovators with an unwavering commitment to results. Join us in developing …

Added Oct 15, 2026

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Amgen

Engineer I

US - California - Thousand Oaks

Full time
Regular

… of the Amgen team. Join us and transform the lives of patients while transforming your career. Engineer I What you will do Let’s do this. Let’s change the world. In this vital role you will support manufacturing …

Added Oct 15, 2026

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Johnson & Johnson

Director, Medical Safety Officer, Oncology

Horsham, Pennsylvania, United States of America +2 locations

Full time
Regular

Johnson & Johnson (J&J) is seeking a Director, Medical Safety Officer, Oncology to be located in Titusville, NJ; Raritan, NJ or Horsham, PA. Our expertise in Innovative …

Added Oct 16, 2026

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Coupang

Principal, EHS Compliance (Construction Safety)

Taipei, Taiwan

Full time (company default)

… risks and impact to leadership. Build and maintain a robust compliance monitoring system for construction safety across all sites. Spearhead efforts to track, assess, and interpret applicable local construction safety …

Added Oct 4, 2026

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Johnson & Johnson

Associate Director, Safety Analysis Scientist

Raritan, New Jersey, United States of America +2 locations

Full time
Regular

Pay posted by employer$137,000–$235,750

Added Oct 15, 2026

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Coupang

Principal, Trust and Safety Compliance

Taipei, Taiwan

Full time (company default)

Strategy Development: Develop and execute the overall Trust and Safety strategy aligned with the company's compliance vision to mitigate risk, address abuse, and foster a safe …

Added Oct 4, 2026

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Boeing

Senior ISS System Safety Engineer

USA - Houston, TX

In person
Full time
Regular

Pay posted by employer$141,100–$190,900

Works with our Safety cross-functional team to lead risk-based hazard analyses at a system level, identify appropriate control …

Added Oct 12, 2026

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Thermo Fisher Scientific

Safety Scientist II/ III, EMEA

Remote, Serbia +9 locations

… and communities depend on – now and in the future. Our detailed, goal-oriented team members manage the safety profile of new drugs in clinical trials, oversee case-processing activities through all phases of …

Added Oct 16, 2026

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Johnson & Johnson

Oncology Global Medical Safety Intern

Horsham, Pennsylvania, United States of America +1 location

Full time
Internship

… on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures. We lead where medicine is going and need innovators with an unwavering commitment to results. Join us in developing …

Added Oct 15, 2026

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Labcorp Holdings

EHS Specialist I

Shanghai, China

Full time
Regular

… implements policies and procedures. May function as Chemical Hygiene Officer, Biosafety Officer, Radiation Safety Officer, Emergency Coordinator or other site technical expert as needed. May function as the EHS Site Key …

Added Oct 15, 2026

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Johnson & Johnson

Principal Scientist I

Shanghai, China

Full time
Regular

Principal Scientist I, Immunology Clinical Biomarker Operations (China) Location: China (Shanghai) Department: Translational …

Added Oct 15, 2026

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Amgen

Specialist Manufacturing I

US - Rhode Island - West Greenwich

Full time
Regular

… team. Join us and transform the lives of patients while transforming your career. Specialist Manufacturing I Duties: Lead and support planning and execution of key initiatives with cross functional teams at the …

Added Oct 15, 2026

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Johnson & Johnson

Director, Medical Safety Officer, Oncology

Horsham, Pennsylvania, United States of America +2 more

Full time
Regular

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About this opportunity

Original employer description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Product Safety

Job Sub Function:

Product Safety Risk Management MD

Job Category:

Scientific/Technology

All Job Posting Locations:

Horsham, Pennsylvania, United States of America, Raritan, New Jersey, United States of America, Titusville, New Jersey, United States of America

Job Description:

Johnson & Johnson (J&J) is seeking a Director, Medical Safety Officer, Oncology to be located in Titusville, NJ; Raritan, NJ or Horsham, PA.

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

The Pharmaceuticals Medical Safety Officer (MSO) has accountability for assessing the medical safety of assigned products and will strategically lead cross-functional matrix teams responsible for product safety and benefit risk oversight and represents Global Medical Safety (GMS) as the product spokesperson regarding overall benefit/risk.

The MSO will report to the Product Safety Head, Cellular Therapy, Hematology and oversee the safety and benefit/risk assessment of assigned products within the Hematology TA that are marketed and/or in clinical development. Collaborating with relevant functions, the MSO will ensure proactive and timely assessments of safety data to characterize the emerging and known safety profiles and benefit-risk assessment of assigned products within the TA. The MSO will communicate potential and known risks and changes to benefit/risk, when appropriate, to the TA Safety Head, the Head of Global Safety Strategy & Risk Management (GSSRM), the Chief Safety Officer (CSO), the Pharmaceuticals Chief Medical Officer (CMO), the Qualified Person for Pharmacovigilance (QPPV) Pharma, Senior Management, Health Authorities (HA), Prescribers and/or Patients. In compliance with legal and regulatory requirements, the MSO will also lead when appropriate, in the design and implementation of risk mitigation strategies to ensure the safe and appropriate use of Innovative Medicine products.

Responsibilities include, but are not limited to the following:

Strategically lead the Safety Management Teams (SMT) for assigned products.
- SMT responsibilities include safety surveillance (including signal detection) and risk management activities [including Risk Management Plan (RMP) and Risk Evaluation and Mitigation Strategy (REMS)], as well as other activities related to managing the safety profile of assigned products.
Provide medical and scientific expertise as the GMS representative on the Compound Development Team (CDT) and Clinical Teams.
Anticipate safety concerns and influence other relevant functions including Clinical teams to minimize/mitigate patient impact by active participation in the design of the clinical protocols.
Be an active partner and core contributor of safety input to key regulatory or clinical documents including:
- Risk management plans.
- Safety development plan.
- Clinical Trial Protocols.
- Informed Consent Forms (ICF).
- Safety Sections of Investigator’s Brochure (IB) and IB addenda.
- Clinical Study Reports (CSR).
- Annual Safety Reports (ASR).
- Integrated Safety Summary (ISS) and Summary of Clinical Safety (SCS) for NDA/BLA/MAA filings.
  Periodic Benefit Risk Evaluation Report (PBRER)/Periodic Safety Update Report (PSUR).
  Health authority queries.
- Core Data Sheets (CDS).
Effectively communicate (verbally and in writing) important results of medical safety and benefit/risk management evaluations, when necessary, to the GMS Leadership Team, CMO, and the Medical Safety Council (MSC).
Actively participate and contribute to meetings with Health Authorities and external key opinion leaders.
Provide medical safety leadership on due diligence teams to evaluate Licensing & Acquisition opportunities.
Provide medical oversight to contractors and non-physician staff involved in preparing written safety evaluations for their assigned products. This will include:
- Defining the safety question or issue requiring medical safety assessment.
- Developing the strategy for the safety review and analysis.
- Interpreting results and determining the medical importance of a question or issue.
- Reviewing and approving (i.e., signatory) medical assessment reports (e.g., ad hoc safety reports).
Work across the GMS TAs to align and improve common processes including providing strong leadership and a harmonized approach across clinical teams for safety data collection, assessment, and safety-related processes and issues.
Assist in the creation, review and implementation of new SOPs, Work Instructions, guidelines, documents, and other tools pertaining to safety assessment and risk management.
Lead or actively participate in department-wide initiatives.

Minimum Qualification:

Physician (MD or equivalent) with 2-5 years of pharmacovigilance (PV) experience or other relevant experience (e.g., Clinical research, Medical Affairs, clinical) required.
Board Certified/Board Eligible/equivalent preferred.
Medical specialization preferred.
Demonstrated skills in clinical medicine with at least 1 year of clinical practice experience.
Demonstrated knowledge of principles of drug development, pharmacology, clinical trial methodology and design, medical monitoring of trials, assessment of drug risks and benefits, and safety assessment of drugs both on the market and in development and global safety regulations highly preferred.
Ability to influence, negotiate and communicate with both internal and external stakeholders.
Experience with Health Authority presentations is preferred.

Required Technical Knowledge and Skills:

Ability to lead global cross-functional teams effectively and strategically.
Connect, collaborate, and build consensus across relevant functions.
Ability to think strategically, have a global mindset, big picture orientation, Ability to see the context of the entire situation, understand implications to the business.
Ability to critically evaluate safety data from multiple sources (clinical trials, environment, literature, etc.), assess clinical importance and potential strategic impact of the data and present the findings clearly in both written and oral communications.
Experience and knowledge of Good Clinical Practices and Pharmacovigilance regulatory requirements in US, the EU and globally, the conduct of clinical trials and for the appropriate contributions to regulatory filings, PV documents and risk management plans.
Able to plan work to meet deadlines and effectively handle multiple priorities.
Excellent verbal and written communication skills, including formal presentation skills. Written skills as evidenced by publication and journal articles are also desirable.
Fluent in written and spoken English.
Proficiency in Word and PowerPoint is desired.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please contact us via https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.

#LI-Hybrid

Required Skills:

Preferred Skills:

Clinical Operations, Compliance Management, Compliance Risk, Consulting, Design Mindset, Developing Others, Leadership, Medicines and Device Development and Regulation, Operational Excellence, Quality Control (QC), Research Ethics, Risk Management, Safety Investigations, Safety-Oriented, Serious Adverse Event Reporting, Standard Operating Procedure (SOP), Succession Planning, Surveillance

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Keywords also found in description

Full time
Product Safety
Regular

Location reference: GeoNames (CC BY 4.0), normalized by Referizz.