Manager, Pharmacovigilance Case Processing

Servier Pharmaceuticals; Boston (MA); Hybrid; USD 131,000 - 150,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Unlimited sick time

401(k)

Job summary

Servier is seeking a Manager, Pharmacovigilance Case Processing in Boston to oversee end-to-end PV case management outsourced to a vendor, from collection to submission. The role partners with internal PV teams, vendors, and cross-functional groups.

Qualifications include a life sciences degree (or PharmD), 4+ years in pharmacovigilance case management, experience with ARGUS and PV regulations, and strong QA/CAPA skills. Hybrid work with 2–3 days in the Boston office; some travel to France.

Qualifications

• Bachelor’s degree in Life Science or PharmD (healthcare professional preferred).
• 4+ years in pharmacovigilance case management with end-to-end AE handling.
• Strong knowledge of PV regulations and ARGUS or similar PV systems.

Responsibilities

• Oversee end-to-end PV case processing for outsourced activities.
• Ensure regulatory compliance and QC of vendor work.
• Coordinate with LPVs, study teams and audits as SME.
• Support trial documentation and vendor training.

Skills

Pharmacovigilance

Data entry

Quality control

CAPA management

Vendor management

Regulatory compliance

Cross-functional collaboration

Education

Bachelor’s degree in Life Science or PharmD

Tools

ARGUS

Job description

Date posted: Aug 6, 2026
City: Boston
Country/Region: US
Type of Contract: Full-time Employment / Unlimited
Job Requisition ID: 12468
Manager, Pharmacovigilance Case Processing

About Servier

Servier in the U.S. is a Boston-based, commercial-stage biopharmaceutical company launched by Servier Group in 2018. As a privately held organization, Servier is uniquely positioned to advance cutting-edge science, tackle underserved therapeutic areas and make patients the focus of every strategic decision.

Role Summary

The Manager, Pharmacovigilance Case Processing is responsible for overseeing the end-to-end management of pharmacovigilance cases outsourced to a vendor, encompassing activities from initial collection to final submission. This role involves close collaboration with internal pharmacovigilance representatives, external case processing vendors, and various cross-functional teams.

Primary Responsibilities

Monitoring Outsourced Activities & Case Management

• Manage pre- and post-marketing pharmacovigilance cases processed by Service provider: book-in, data entry, coding, narratives, quality control, medical review, and submission of applicable cases.
• Ensure compliance with regulatory requirements, Safety Data Exchange Agreements (SDEA), and internal procedures.
• Perform weekly quality control of cases processed by vendors.
• Draft and validate deviation forms, root cause analysis, and CAPAs for cases submitted late to Regulatory authorities and other applicable recipients

Clinical Trial Support & Documentation

• Review protocols and electronic case report forms (eCRFs); write Safety Management Plans (SMP) for clinical trials.
• Request updates for ARGUS database configurations (studies, products, reporting rules, etc.,).
• Provide necessary documentation and training to vendors to ensure high-quality outsourced activities.

Coordination & Oversight

• Perform reconciliation with business partners, Local Pharmacovigilance teams (LPVs), and clinical databases.
• Participate in study kick-off/end meetings, operational meetings with vendors/business partners, and in audits/inspections as a Subject Matter Expert (SME).
• Contribute to process optimization, quality document writing, and the validation of vendor invoices.

Education And Required Skills

• Bachelor’s degree in Life Science or a PharmD, preferably a healthcare professional (e.g., Medicine, Pharmacy, or Life Sciences).
• Minimum of 4 years of experience in pharmacovigilance case management, involving investigational drugs and/or approved products with end-to-end adverse event management in prominent global safety databases.
• Strong working knowledge of international pharmacovigilance (PV) regulations and reporting requirements
• Hands-on experience with pharmacovigilance databases (e.g., ARGUS) and other safety information systems
• Understanding of literature review processes for safety signal identification
• Demonstrated experience in quality control, CAPA management, and KPI development/monitoring for case processing activities
• Proven ability to manage outsourced PV activities, including performance monitoring and training of external partners/Local pharmacovigilance teams (LPVs)
• Ability to collaborate effectively across global teams and serve as SME during audits and/or inspections.

Travel and Location

• Hybrid model preferred, with 2-3 days a week in the Boston office
• Occasional travel to the France headquarters may be required

Job Description

Candidate Profile

Servier’s Commitment

Servier is committed to modeling diversity, equity, and inclusion within the industry. We are dedicated to fostering an environment that maintains equitable treatment for all and we welcome applicants who are passionate, committed, and innovative individuals. We encourage candidates to apply to our open roles as we are always willing to consider experiences and skills beyond what is listed in the job description.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Salary Range

The salary range for this role is $131,000 - $150,000. An employee’s pay position within the salary range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, and business or organizational needs. We may ultimately pay more or less than the posted range, and the range may be modified in the future.

Employees in this position are also eligible for Short-Term and Long-Term incentive programs.

• medical
• dental
• vision
• flexible time off (Servier provides unlimited sick time and flex time, and does not accrue time off)
• 401(k)
• life and disability insurance
• recognition programs
• other great benefits (all benefits are subject to eligibility requirements)

Nearest Major Market: Boston