Remote Global Oncology Pharmacovigilance Manager

Ladders; United States; Remote; USD 116,000 - 157,000; Full time

Job summary

Ladders is seeking a Global Pharmacovigilance (PV) Scientist, Manager- Oncology to help shape global drug safety strategy for an oncology portfolio, with emphasis on signal detection, evaluation, and aggregate reporting. Remote - US based candidates only, no visa sponsorship.

Responsibilities include leading signal detection, evaluating adverse events, and providing strategic safety input into protocols and study reports. Collaboration across clinical, safety, and governance teams is essential.

Qualifications

• Doctorate degree or equivalent experience in pharmacovigilance.
• Master's degree with 2 years of experience, Bachelor's with 4 years, or Associate with 8 years of industry experience.
• 5+ years of pharmacovigilance or drug safety experience in biotech or pharmaceutical settings preferred.
• Experience in signal detection, evaluation, and management activities.
• Proven ability to influence and lead in a cross-functional environment.

Responsibilities

• Lead signal detection and management activities using multiple safety data sources.
• Conduct scientific evaluations of adverse events from clinical trials and external data.
• Prepare and submit aggregate safety reports while maintaining scientific integrity.
• Provide strategic safety input into clinical protocols and study reports.
• Collaborate with cross-functional teams to support safety governance and decision-making.

Skills

Pharmacovigilance

Signal detection

Cross-functional collaboration

Leadership

Regulatory compliance

Education

Doctorate in pharmacovigilance or equivalent

Master's degree in life sciences

Bachelor's degree in related field

Associate's degree in related field

Job description

Ladders is seeking a Global Pharmacovigilance (PV) Scientist, Manager- Oncology to help shape global drug safety strategy for an oncology portfolio, with emphasis on signal detection, evaluation, and aggregate reporting. Remote - US based candidates only, no visa sponsorship.

Responsibilities include leading signal detection, evaluating adverse events, and providing strategic safety input into protocols and study reports. Collaboration across clinical, safety, and governance teams is essential.