253 matching jobs for “Safety Data Lead I”

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Gilead Sciences

Senior Director, Epidemiology and RWE Oncology Franchise Lead

Dublin, Ireland

Full time
Regular

The Epidemiology and Real-World Evidence (EpiRWE) function at Gilead is part of the Clinical Data Sciences (CDS) group within the Clinical Development organization and aims to unlock the power of …

Added Oct 15, 2026

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Gilead Sciences

Senior Director, RWE Lead in Inflammation Therapeutic Areas

Foster City, California, United States +1 location

Full time
Regular

Pay posted by employer$261,375–$338,250

The Real-World Evidence (RWE) function at Gilead is part of the Clinical Data Sciences (CDS) group within the Clinical Development organization and aims to unlock the power of …

Added Oct 15, 2026

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Boeing

F-15 Flight Plan - Systems Engineer Integrator Lead

USA - Berkeley, MO

In person
Full time
Regular

Pay posted by employer$136,850–$185,150

Lead the analysis of complex performance requirements, operational concepts, and functional requirements to …

Added Oct 12, 2026

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Boeing

Lead or Senior Satellite Systems Ground Systems Engineer

USA - El Segundo, CA +1 location

In person
Full time
Regular

Pay posted by employer$146,200–$197,800

Lead or Senior Satellite Systems Ground Systems Engineer Company: The Boeing Company The Boeing Space & Mission …

Added Oct 12, 2026

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Bristol-Myers Squibb

Director, Medical Evidence Generation Operations Lead (Multiple Openings)

Princeton - NJ - US +3 locations

Full time
Regular

Pay posted by employer$213,300–$258,468

… work that transforms the lives of patients, and the careers of those who do it. The Director MEG Operations Lead provides strategic and operational leadership for the Medical Evidence Generation (MEG) trial portfolio …

Added Oct 15, 2026

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Boeing

Controls Matlab & Simulink Engineer (Associate, Mid-Level, or Lead)

USA - Kirtland AFB, NM +1 location

Full time
Regular

Pay posted by employer$91,800–$124,200

Perform hands-on mathematical modeling, simulation, and data analysis Analyze system behavior, including stability, linearity, and transient/steady-state responses …

Added Oct 12, 2026

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Boeing

Spacecraft Command and Data Handling (C&DH) Engineer - Millennium Space Systems

USA - El Segundo, CA

In person

Pay posted by employer$98,600–$145,000

… objectives and constraints Select avionics and onboard processing units that meet flight software (FSW) and data handling needs while balancing performance, power, mass, and cost Perform requirements definition and flow …

Added Oct 12, 2026

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Merck (MSD)

Field Medical Affairs, Team Lead - Eastern US – Pulmonary Hypertension

USA - REMOTE - REMOTE

Pay posted by employer$210,400–$331,100

Role Summary The Field Medical Affairs, Team Lead of US Medical Affairs (USMA) drives strategic clarity, operational excellence, and cross-functional …

Added Oct 16, 2026

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Boeing

Mid-Level, Lead or Senior Satellite Systems Ground Systems Engineer

USA - El Segundo, CA

In person
Full time
Regular

Pay posted by employer$119,850–$162,150

Mid-Level, Lead or Senior Satellite Systems Ground Systems Engineer Company: The Boeing Company The Boeing Space & Mission …

Added Oct 12, 2026

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The Cigna Group

Electro-Mechanical Controls Engineer (Automation Engineer Lead Analyst) - Express Scripts

Newark, Delaware, United States +1 location

Full time
Regular

… pharmacy production equipment through preventive, corrective, and emergency maintenance activities. Lead troubleshooting efforts for complex electrical, mechanical, pneumatic, PLC, and computer-controlled systems …

Added Oct 16, 2026

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Johnson & Johnson

[Innovative Medicine] R&D, Experienced I Stat Programmer, Clinical & Statistical Programming Japan, Global Development

Chiyoda, Japan

Full time
Regular

Position Summary: The Experienced Programmer is an individual contributor with knowledge of data structures, industry standards, programming languages, and programming methods. This role supports data …

Added Oct 15, 2026

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Gilead Sciences

Associate Director, Operations Oversight Lead Medical Affairs Research Global Operations (MARGO)

Uxbridge, United Kingdom

Full time
Regular

… across research, development, post-approval, and commercialization. Observational research is conducted on data collected from individuals assessed for biomedical, health and other outcomes, and includes observational …

Added Oct 15, 2026

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Johnson & Johnson

Senior Material Surface Technology Engineer

Suzhou, Jiangsu, China

Full time
Temporary

Lead new engineering project and delivery on schedule （领导新的工程项目，按时完成交付任务） Plan, design, develop and implement …

Added Oct 15, 2026

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KLA

Senior Electrical Systems Engineer

Allentown, Pennsylvania, United States

Full time
Regular

Pay posted by employer$100,100–$146,833 per year

… including advanced etch and deposition systems. This role combines electrical system design, product safety, regulatory compliance, sustaining engineering, and new product development. The ideal candidate is a …

Added Oct 15, 2026

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Coupang

Area Manager (Taichung)

Taichung, Taiwan

Full time (company default)

Lead and Scale Regional Operations: Oversee day-to-day fulfillment and logistics operations across your …

Added Oct 4, 2026

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Coupang

Camp manager [L5]

Taoyuan, Taiwan

Full time (company default)

Lead and Scale Regional Operations: Oversee day-to-day fulfillment and logistics operations across your …

Added Oct 23, 2026

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Coupang

Area Manager (Tainan)

Tainan, Taiwan

Full time (company default)

Lead and Scale Regional Operations: Oversee day-to-day fulfillment and logistics operations across your …

Added Oct 4, 2026

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Thermo Fisher Scientific

Medical Director - Principal Investigator

Prague, Czechia

… on – now and in the future. Day to day responsibilities: The Medical Director of our Integrated Phase I - IV clinic serves as a Principal Investigator and senior medical authority for the clinic, providing …

Added Oct 16, 2026

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Bristol-Myers Squibb

Director, Global Clinical Physician - Early HOCT

Cambridge Crossing - MA - US

Full time
Regular

Pay posted by employer$308,700–$374,075

… a primary source of medical accountability and oversight for multiple clinical trials · Manages Phase I/II studies, with demonstrated decision making capabilities, · Provides medical and scientific …

Added Oct 18, 2026

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Thermo Fisher Scientific

Supervisor, Kit Production

Vilvoorde, Belgium

… the environment, making sure our food is safe or helping find cures for cancer. Position Overview: Lead and develop a high-performing manufacturing team to execute production schedules with precision, uphold …

Added Oct 16, 2026

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Gilead Sciences

Senior Director, Epidemiology and RWE Oncology Franchise Lead

Dublin, Ireland

Full time
Regular

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About this opportunity

Original employer description

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.

Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.

Job Description

The Epidemiology and Real-World Evidence (EpiRWE) function at Gilead is part of the Clinical Data Sciences (CDS) group within the Clinical Development organization and aims to unlock the power of Real-World Data (RWD) to help transform innovations to life-changing medicines for patients. The Senior Director, EpiRWE Oncology Franchise Lead in Early Development reports to the Executive Director, EpiRWE Therapeutic Area (TA) Head-Oncology and is accountable for the development and execution of the RWE strategy in support of one or more Oncology Franchises under development. The incumbent will serve as the key EpiRWE subject matter expert within the Early Development teams (Gilead Asset Team (GAT), Early Molecule Teams (EMTs) and Development Evidence Teams (DETs)) for the relevant products within an Oncology Franchise and all its indications across the development lifecycle and serve as a strategic partner to clinical development, medical, and commercial teams to ensure excellence in the generation and use of RWE at the global level.

The SD, EpiRWE Oncology Franchise Lead will ensure the timeliness, quality, and utility of EpiRWE required by internal and external stakeholders (e.g.regulators), as well as advise on methodological approaches in support of payer and provider interactions.

Success in this role requires excellence in design and conduct of epidemiologic studies/analyses, direct expertise in use of EpiRWE at early stages of the product Oncology Franchise development process, and the ability to lead and manage cross-functional efforts and resources.

Duties & Responsibilities

Serve as the single point of accountability for the development, execution, and communication of the global EpiRWE strategy supporting early-stage clinical development evidence requirements for a specific Oncology Franchise and its pipeline/lifecycle indications in Oncology.
Ensure the use of robust scientific methods and fit-for-purpose data resources for the timely execution of the EpiRWE strategy, in alignment with the clinical development plan and broader EMT, DET and GAT objectives.
Provide the functional perspective and subject-matter expertise, especially regarding regulatory use of EpiRWE, as a member of the EMTs and situational member of the DET.
Deliver, within time, budget, and quality standards, proactive EpiRWE generation including, but not limited to: natural history of disease, population characterization, assessment of treatment patterns and unmet need, development of external comparators, benchmarking of clinical outcomes and comparative safety and effectiveness research.
Communicate effectively about the utility of EpiRWE across the product Oncology Franchise lifecycle and drive use of study/analysis results to support internal and external decisions across the Franchise.
Ensure expert communication of observational research results, including development of pertinent sections of regulatory documents, publications, white papers, press releases, etc.
Oversee timely and appropriate development of epidemiological sections of regulatory documents for agencies worldwide (e.g., Risk Management Plan, orphan or breakthrough designations, Pediatric Investigation Plan, query responses, advisory committee briefing documents).
Represent the EpiRWE function in internal cross-functional initiatives and external organizations, such as industry associations, professional societies, or regulatory working groups.
Foster close collaborations with quantitative functions within CDS (e.g., Biostatistics, Bioinformatics, Clinical Pharmacology), as well as in Research, Clinical Research, Medical Affairs, and Global Value and Access to anticipate and meet the evidence needs of regulators, payers, providers, and patients.
Actively identify the need for the development of processes or gaps in training documents aimed at increasing the efficiency, quality, and impact of functional activities.

Requirements

Doctoral degree (e.g. PhD, MD, ScD, PharmD) and/or Master’s degree (e.g. MSc) in Epidemiology or related discipline, such as Outcomes Research, Medicine, Biostatistics from an accredited institution, with a minimum of twelve (12) years of relevant, post-graduation experience; preference for a minimum of six (6) years of that experience to be in the biopharmaceutical industry.
A strong track record of scientific publications demonstrating expertise in observational study design, analysis, and interpretation and direct experience with different applications of Epidemiology and RWE, especially in support of early-stage clinical development and regulatory approvals.
Demonstrated understanding of the Oncology therapeutic area, including disease knowledge, current treatment practice and guidelines, pertinent clinical trial endpoints and safety outcomes.
Demonstrated ability to function with a high level of autonomy and develop productive cross-functional collaborations.
Ability to manage priorities, resources, and performance targets, in a changing environment.
Ability to communicate proactively with others across functions to ensure shared purpose and clear accountability for future decisions.Well-developed cross-cultural sensitivity.

Equal Employment Opportunity (EEO)

It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual’s gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.

For Current Gilead Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.

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Keywords also found in description

Clinical Development Group
Full time
Regular

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