SERM Scientific Director

GSK

Scientific Director providing scientific expertise in safety evaluation for oncology development. Leading risk management and communication strategies to enhance patient outcomes across global portfolios.

Posted 6/6/2026full-timeMassachusetts, Pennsylvania • 🇺🇸 United StatesLead💰 $169,950 - $283,250 per yearWebsite

About the role

Key responsibilities & impact

Provides advanced scientific expertise in the safety evaluation and risk management of key GSK oncology assets in clinical development.
Leads the identification, assessment, and communication of safety risks to ensure robust benefit-risk profiles and protection of patients globally.
Drives the evaluation and interpretation of safety data, including signal detection and assessment.
Mentors and coaches junior team members as applicable.

Requirements

What you’ll need

Degree in a health or life sciences discipline (e.g., Bachelor of Science, PharmD, MD, PhD, or equivalent).
Minimum 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.

Benefits

Comp & perks

Health care and other insurance benefits (for employee and family)
Retirement benefits
Paid holidays
Vacation
Paid caregiver/parental and medical leave

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

pharmacovigilancedrug safetysignal detectionsafety surveillancerisk managementclinical developmentsafety evaluationdata interpretationbenefit-risk assessmentsafety data evaluation

Soft Skills

mentoringcoachingcommunicationscientific judgementinterpersonal skills

Certifications

Bachelor of SciencePharmDMDPhD