Senior Physician, Patient Safety

When our values align, there's no limit to what we can achieve.   At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Senior Physician, Patient Safety performs medical, safety monitoring or pharmacovigilance activities for assigned projects. They provide medical reviews, analysis and guidance in all required safety reports. Senior Physician, Patient Safety will act as Subject Matter Expert in therapeutic areas and mentor junior team members while working on complex tasks requiring in-depth evaluation. Key Accountabilities: General Maintaining a good working knowledge of the Adverse event/Safety profile of assigned products, labeling documents, data handling conventions, client’s guidelines and procedures, and global drug safety regulations and guidelines Maintaining an awareness of global regulatory requirements, reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for adverse event reporting Communicating and discussing issues related to review process with Line Manager/ Project Leader/Designee Interacting with internal and external stakeholders for resolving issues Attending and/ or presenting at client/cross functional meetings along with other stakeholders. Working as Subject Matter Experts (SMEs) Assisting the Project Lead/Functional Lead for audits and inspections Provides inputs for process improvements Works closely with Project Lead/Functional Lead for process co-ordination and to ensure meeting all Key Performance Indicators (KPIs) for the process Function as pharmacovigilance representative/safety scientist Attend/support Bid defense meetings Actively mentoring Patient Safety Physicians to develop their skills and expertise Case report medical review (as applicable) Performing medical review of cases not limited to (including complex and challenging cases requiring expert judgement)), clinical trial, and literature cases including combination products {drug-device}) according to client/Parexel Standard Operating Procedures (SOPs; as applicable) and liaising with the client, as require Writing Pharmacovigilance/Marketing Authorization Holder (MAH) comment and assessing company causality Review appropriateness of medical content in narrative for medical coherence Assessing seriousness, listedness / expectedness of reported events. Providing medical inputs to case processing team Raising appropriate follow-up queries for relevant information from the reporter/HCP (Health Care Professional) Review and verify appropriate selection of adverse events from source documents, assign appropriate Medical Dictionary for Regulatory Activities (MedDRA) code, review narrative Identify and resolve case issues, coordinate with client therapeutic/legal team Provide guidance to junior physicians on case assessment methodologies Skills: Experience in clinical medicine (general or specialist qualifications) which is expected to be kept up to date Demonstrated success in technical proficiency and scientific creativity Ability to work on complex tasks requiring in-depth evaluation Good knowledge of drug safety and the drug development process Ability to exercise judgment within broadly defined practices and policies Good presentation and verbal/written communication skills Good interpersonal skills Client focused approach to work Computer proficiency, an ability to work with web-based applications and familiarity with the Windows operating system and Microsoft Office apps An ability to comprehend various regulatory or client requests and be able to strategize a handling approach Experience mentoring junior team members A flexible attitude with respect to work assignments and new learnings An ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail An ability to assess the clinical relevance of medical data and to interpret its clinical meaning is essential A willingness to work in a matrix environment and to value the importance of teamwork Strong knowledge of international drug regulation including ICH GCP, GVP, and all other applicable regulations and guidelines Knowledge and Experience: 3 Years of relevant experience in pharmacovigilance Good knowledge/understanding of medical terminology Education: Bachelor of Medicine, Bachelor of Surgery (MBBS) / Doctor of Medicine (MD)/ Medically qualified from an acknowledged Medical School Completion of at least basic training in clinical medicine (residency, internship etc.)