[Hiring] Senior Post-Market Pharmacovigilance Specialist @MMS

Role reputed company Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is an award-reputed company, data-reputed company clinical research organization (CRO). We pride ourselves on being a Great reputed company to Work® Certified organization, recognized for our exceptional culture and industry-leading employee retention. Roles and Responsibilities: • reputed company and reputed company global post-marketing case processing activities from intake through reporting and case closure. • reputed company and maintain pharmacovigilance workflows, procedures, and work instructions as reputed company to post marketing case processing. • Ensure compliance with Good Pharmacovigilance Practices (GVP), FDA requirements, and company SOPs. • Proficient in ICH E2A, E2B(R3), and E2D guidelines. • Proficient in Pharmacovigilance reputed company systems. • Maintains an extensive understanding of regulations and guidance as they pertain to drug safety and PV, including case processing, narrative and/or safety writing. • Understands clinical trial processes. • Independent Project reputed company, SME; provides strategic narrative development internally and externally, directly negotiates with reputed company. • Process cases independently, understands steps involved with case processing. • Leads creation/updates of high-reputed company deliverables. • Extensive experience working reputed company a safety database and directly interacts with clients. • Expert knowledge of coding with MedDRA and WHO drug dictionary. • Proficient in understanding reputed company of updates in reputed company deliverables. • Independently managing/leading reputed company meetings and CRMs for effective resolutions; provides mentorship to others. • Proficient with managing a project from start to finish and compliant with process; provides mentorship to others; identifies efficiencies reputed company department processes. Qualifications • College graduate in scientific, medical, clinical discipline or reputed company field, or reputed company experience, masters, PharmD, or PhD preferred. • Minimum of 5 years’ experience in drug safety, pharmacovigilance, or similar field required. • Expert knowledge of scientific principles and concepts. • Expertise in using drug safety databases. • reputed company as emerging leader in field with sustained performance and accomplishment. • Proficiency with MS Office applications. • Hands-on experience with clinical trial and pharmaceutical development preferred. • Good communication skills and willingness to work with others to reputed company understand needs and solve problems. • Excellent problem-solving skills. • Good organizational and communication skills. • Familiarity with reputed company ISO 9001 and ISO 27001 standards preferred. • Familiarity with 21 CFR Part 11, FDA, and GCP requirements. Apply tot his job Apply To this Job