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Director, Pharmacovigilance Operations (Maritide Lead)

Amgen
Amgen
6-8 years
188,143.00 USD - 227,444.00 USD
10 Nov. 5, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Position Title:

Director, Pharmacovigilance Operations (MariTide Lead)

Location: United States (Remote)
Job ID: R-228098
Category: Safety
Work Type: Remote
Date Posted: November 3, 2025
Salary Range: USD 188,143 – 227,444


About Amgen

At Amgen, we believe you’re part of something greater — a shared mission to serve patients living with serious illnesses.

Since 1980, Amgen has been at the forefront of biotechnology, pioneering new therapies in four major therapeutic areas:

  • Oncology

  • Inflammation

  • General Medicine

  • Rare Disease

Every day, we strive to develop and deliver life-changing medicines that help patients live longer, fuller, and healthier lives.


Role Overview

In this vital role, the Director, Pharmacovigilance Operations (MariTide Lead) will serve as the US/EU Local Safety Officer and primary FDA/EMA point of contact for safety reporting.
The role involves leading global safety case management operations, ensuring compliance with regulatory requirements, and maintaining inspection readiness for the Rare Disease portfolio.


Key Responsibilities

Leadership and Oversight

  • Oversee all individual case safety report (ICSR) processing and submissions to regulatory authorities (FDA/EMA), business partners, and vendors.

  • Manage all vendor interactions and oversight for case intake, adverse events, and product complaint triage.

  • Ensure compliance with approved processes, training, and audit requirements.

Safety Process Ownership

  • Serve as Business Process Owner (BPO) for Adverse Event (AE) Intake processes across the MariTide platform and Rare Disease portfolio.

  • Lead training, controlled documentation, and systems management for safety operations.

  • Act as subject matter expert for Data Element Standards Committee, ensuring compliance in eCRF/CRF design and data collection for both clinical trials and post-market activities.

Compliance and Governance

  • Ensure all Pharmacovigilance Agreements (PVAs) comply with global safety regulations.

  • Support Qualified Person for Pharmacovigilance (QPPV) delegated activities and maintain inspection readiness as outlined in the PV System Master File.

  • Serve as Inspection and Audit Point of Contact (POC) for health authorities.

  • Lead eSAE Governance and oversee CAPA implementation and quality improvement actions.

Process Improvement and Innovation

  • Evaluate and implement process improvement strategies within the ICMC (Integrated Case Management and Compliance) team.

  • Own process deliverables, performance metrics, and compliance KPIs.

  • Lead or support eSAE process implementation across Global Patient Safety (GPS) and Global Development Operations (GDO).

Cross-functional Collaboration

  • Act as liaison between Clinical Trial teams and Global Patient Safety to ensure accurate adverse event capture.

  • Develop and maintain strong cross-functional relationships across global teams.

  • Contribute to SOP development, R&D Standards, and training materials.


Basic Qualifications

  • Doctorate degree with 4+ years of Drug Safety or Life Sciences experience
    OR

  • Master’s degree with 7+ years of Drug Safety or Life Sciences experience
    OR

  • Bachelor’s degree with 9+ years of Drug Safety or Life Sciences experience


Preferred Qualifications

  • Degree in Life Sciences, MPH, RN, or other healthcare professions

  • 8+ years of relevant experience, including 6+ years in Drug Safety

  • Proven leadership and team management experience

  • Strong understanding of pharmacovigilance regulations and global safety systems

  • Ability to lead inspections, audits, and manage cross-functional communications


What You Can Expect from Amgen

Amgen is committed to supporting your professional growth, well-being, and work-life balance.

Our Total Rewards Plan includes:

  • Comprehensive Retirement and Savings Plan with company contributions

  • Medical, dental, and vision insurance coverage for staff and dependents

  • Life and disability insurance, and flexible spending accounts

  • Discretionary annual bonus program or sales-based incentive plans

  • Stock-based long-term incentives

  • Award-winning time-off plans

  • Flexible work models, including remote and hybrid arrangements

Actual salary will depend on skills, experience, and qualifications.


Additional Information

  • Application Deadline: No fixed deadline; applications accepted until position is filled.

  • Sponsorship: Not guaranteed for this role.


Equal Opportunity & Accessibility

Amgen is an Equal Opportunity Employer and prohibits discrimination based on race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability.

We provide reasonable accommodations for individuals with disabilities during the hiring process and for essential job functions.


How to Apply

Be part of a mission that transforms lives — including your own.

🔗 Apply now at: careers.amgen.com
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