Senior Oncology Safety & Risk Director

GSK; Waltham (MA); Híbrido; USD 218.000 - 363.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health care & family insurance

Retirement benefits

Paid holidays

Vacation

Parental and medical leave

Descripción de la vacante

GSK is seeking a Scientific Director of Safety Evaluation and Risk Management for oncology assets in clinical development. You will lead pharmacovigilance activities, shape safety strategy, and collaborate across functions to ensure robust benefit-risk profiles.

The role emphasizes risk mitigation, regulatory interactions, and global safety oversight. Based in the United States with hybrid on-site expectations, you will mentor teams, present at governance meetings, and drive continuous safety

Formación

• Degree in a health or life sciences discipline (e.g., Bachelor of Science, PharmD, MD, PhD, or equivalent).
• 5+ years experience in pharmacovigilance, drug safety, or related safety evaluation role in the pharmaceutical or biotech industry.
• Practical experience in signal detection, safety surveillance and risk management across clinical development and post-marketing.
• Knowledge of global pharmacovigilance requirements and drug development processes.
• Strong clinical or scientific judgement with experience interpreting clinical and safety data.

Responsabilidades

• Lead pharmacovigilance activities and risk mitigation strategies for assigned oncology assets and clinical trials.
• Drive the evaluation and interpretation of safety data, including signal detection and assessment.
• Develop strategic approaches for safety issue evaluation within clinical development programs.
• Contribute to safety components of global regulatory submissions (e.g., INDs, DSURs, IBs).
• Perform literature review, clinical data synthesis, and integrated safety analyses to inform decision-making.
• Ensure high-quality, timely delivery of outputs while managing multiple priorities.

Conocimientos

Digital Fluency

Enterprise Leadership

Influencing Without Authority

Pharmacovigilance

Presentation Techniques

Educación

Bachelor's in health or life sciences

PharmD/MD/PhD (preferred)

Descripción del empleo

GSK is seeking a Scientific Director of Safety Evaluation and Risk Management for oncology assets in clinical development. You will lead pharmacovigilance activities, shape safety strategy, and collaborate across functions to ensure robust benefit-risk profiles.

The role emphasizes risk mitigation, regulatory interactions, and global safety oversight. Based in the United States with hybrid on-site expectations, you will mentor teams, present at governance meetings, and drive continuous safety