Senior Post-Market Pharmacovigilance Specialist (Remote)

About the role

MMS is an award-winning, data-focused clinical research organization (CRO) supporting the pharmaceutical, biotech, and medical device industries with a proven scientific approach to complex trial data and regulatory submission challenges. As a Great Place to Work® Certified organization, we offer a collaborative and inclusive environment where your contributions truly matter. This role will lead and oversee global post-marketing case processing activities while ensuring compliance with pharmacovigilance standards and regulations.

Responsibilities

• Lead and oversee global post-marketing case processing activities from intake through reporting and case closure
• Develop and maintain pharmacovigilance workflows, procedures, and work instructions for post-marketing case processing
• Ensure compliance with Good Pharmacovigilance Practices (GVP), FDA requirements, and company SOPs
• Apply expertise in ICH E2A, E2B(R3), and E2D guidelines, as well as pharmacovigilance quality systems
• Maintain an extensive understanding of regulations and guidance related to drug safety, PV, case processing, narrative writing, and clinical trial processes
• Serve as an independent project lead and subject matter expert (SME), providing strategic narrative development and direct client negotiations
• Process cases independently, lead the creation and updates of high-quality deliverables, and mentor team members
• Work within a safety database, interact directly with clients, and demonstrate expert knowledge of MedDRA and WHO drug dictionary coding
• Assess the impact of updates on related deliverables and identify process efficiencies
• Independently manage and lead client meetings and CRMs to drive effective resolutions
• Manage projects from start to finish in compliance with established processes

Requirements

• College graduate in a scientific, medical, clinical discipline, or related field (masters, PharmD, or PhD preferred)
• Minimum of 5 years’ experience in drug safety, pharmacovigilance, or a similar field
• Expert knowledge of scientific principles and concepts, with hands-on experience using drug safety databases
• Emerging leader in the field with a track record of sustained performance and accomplishment
• Proficiency with MS Office applications; clinical trial and pharmaceutical development experience preferred
• Strong communication, problem-solving, and organizational skills
• Familiarity with ISO 9001, ISO 27001 standards, 21 CFR Part 11, FDA, and GCP requirements