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 and you can thrive alongside a supportive, innovative team.

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 as related to 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
• Maintain an extensive understanding of regulations and guidance related to drug safety and pharmacovigilance, including case processing, narrative writing, and clinical trial processes
• Serve as an independent project lead and subject-matter expert; provide strategic narrative development internally and externally, and negotiate directly with clients
• Process cases independently, lead creation and updates of high-quality deliverables, and identify process efficiencies
• Work within a safety database, interact directly with clients, and demonstrate expert knowledge of coding with MedDRA and WHO drug dictionary
• Understand the impact of updates on related deliverables
• Independently manage and lead client meetings and CRMs to achieve effective resolutions; mentor others
• Manage projects from start to finish in compliance with processes; mentor others and identify departmental efficiencies

Requirements

• College graduate in a scientific, medical, clinical discipline, or related field; master’s, PharmD, or PhD preferred
• Minimum of 5 years’ experience in drug safety, pharmacovigilance, or a similar field
• Expert knowledge of scientific principles and concepts, and expertise in using drug safety databases
• Reputation as an emerging leader in the field with sustained performance and accomplishment
• Proficiency with MS Office applications
• Hands-on experience with clinical trial and pharmaceutical development preferred
• Strong communication, problem-solving, and organizational skills
• Willingness to collaborate and clearly understand needs to solve problems
• Familiarity with current ISO 9001 and ISO 27001 standards preferred
• Familiarity with 21 CFR Part 11, FDA, and GCP requirements