Global Pharmacovigilance (PV) Scientist, Manager- Oncology

Ladders; United States; À distance; USD 116 000 - 157 000; Plein temps

Résumé du poste

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.

Responsabilités

• 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.

Connaissances

Pharmacovigilance

Signal detection

Cross-functional collaboration

Leadership

Regulatory compliance

Formation

Doctorate in pharmacovigilance or equivalent

Master's degree in life sciences

Bachelor's degree in related field

Associate's degree in related field

Description du poste

For our client, we are seeking a Global Pharmacovigilance (PV) Scientist, Manager- Oncology to join the team of a leader in the Pharmaceuticals & Biotech space. This role will help shape global drug safety strategy for an oncology portfolio, with a strong emphasis on signal detection, scientific evaluation, and aggregate reporting. You will partner closely with clinical, safety, and cross-functional stakeholders to ensure high-quality safety oversight and informed decision-making. The position requires both scientific rigor and the ability to influence across functions in a highly regulated environment. Location: Remote - US based candidates only, no visa sponsorship available Compensation: $116,167 – $157,168 annually Our client is an equal opportunity employer.

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.

Qualifications

• Doctorate degree or equivalent experience in pharmacovigilance.
• Master's degree with 2 years of experience, Bachelor's degree with 4 years of experience, or Associate's degree 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.

Benefits

• Comprehensive employee benefits package including medical, dental, and vision coverage.
• Retirement and savings plan with generous company contributions.
• Discretionary annual bonus program and stock-based long-term incentives.
• Award-winning time-off plans and flexible work models where applicable.
• Career development opportunities to support professional growth.