Global Drug Safety & PV Physician Lead

Genmab; Utrecht; On-site; EUR 179,000 - 269,000; Full time

Benefits offered by this job

401(k) Match

Comprehensive health benefits

Parental leave

Tuition reimbursement

Job summary

Genmab is seeking a medical professional to provide oversight of product safety, conduct adverse event reviews, and manage ongoing safety surveillance. You will collaborate across functions, contribute to regulatory deliverables, and lead safety committees to ensure compliance and inspection readiness.

Ideal candidates hold an MD or equivalent, with 8+ years in pharmacovigilance or clinical development and proven leadership.

Qualifications

• MD or equivalent medical degree with clinical experience.
• Experience in pharmacovigilance, drug safety, or clinical development (8+ years).
• Experience providing medical safety input to trials and regulatory deliverables.

Responsibilities

• Perform medical review of Adverse Events reports for Genmab products.
• Conduct ongoing safety surveillance from clinical trials.
• Lead safety committees and external Data Monitoring Committees (DMCs).
• Provide input to protocols, CRFs, DSURs, and ISRs; prepare safety summaries.

Skills

Pharmacovigilance

Safety surveillance

Medical review

Leadership

Cross-functional collaboration

Education

MD or equivalent

Job description

Genmab is seeking a medical professional to provide oversight of product safety, conduct adverse event reviews, and manage ongoing safety surveillance. You will collaborate across functions, contribute to regulatory deliverables, and lead safety committees to ensure compliance and inspection readiness.

Ideal candidates hold an MD or equivalent, with 8+ years in pharmacovigilance or clinical development and proven leadership.