Prajakta Sutar

Monitor and evaluate the safety of drugs across clinical and post-marketing phases. Review and medically assess adverse event and safety reports. Perform causality, seriousness, and expectedness assessments. · Key Responsibilities: Ensure compliance with global pharmacovigilance ...

The Project Coordinator will be responsible for day-to-day administrative tasks related to TransPerfect's literature monitoring projects. · This role will focus on support functions for the wider Production team, · ensuring all client deadlines are met.Oversee administrative elem ...

The PrimeVigilance Medical Writer position offers a unique opportunity to further develop your career in the field of drug safety. · Key Responsibilities: · Independent authoring, editing, and reviewing of various regulatory/clinical documents (e.g., aggregate reports, risk manag ...