Pharmacovigilance Job at Thermo Fisher
Are you a medical professional passionate about ensuring the safety of groundbreaking therapies? Thermo Fisher Scientific offers a unique opportunity to work as a Pharmacovigilance Physician in a remote capacity. This Remote Pharmacovigilance Job is pivotal in maintaining regulatory compliance while contributing to the development of life-changing treatments. Qualified candidates can play a crucial part in advancing global healthcare standards. Explore this chance to impact the future of medicine with Thermo Fisher Scientific.
About Thermo Fisher Scientific:
Thermo Fisher Scientific is a leading global contract research organisation (CRO) specialising in clinical research services. The company is dedicated to advancing healthcare by providing comprehensive support for drug development and clinical trials. With a commitment to innovation, Thermo Fisher collaborates with pharmaceutical companies and biotechs worldwide to bring effective therapies to market.
Job Details:
- Designation: Pharmacovigilance Physician
- Location: Remote, India
- Job ID: R-01367929
- Job Type: Full-time
- Category: Clinical Research
- Work Schedule: Standard (Mon-Fri)
- Environmental Conditions: Office
Job Description:
The Pharmacovigilance Physician provides medical oversight of pharmacovigilance activities to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed. This role involves attending and presenting at sponsor meetings, providing medical and pharmacovigilance consultation to clients and project team members, and supporting business development activities. The physician will also conduct medical reviews and analyses for clinical trial serious adverse events and marketed products, ensuring thorough assessment and reporting of safety data.
Key Responsibilities:
- Manage all medical aspects of contracted pharmacovigilance tasks across the pharmaceutical product life cycle.
- Adhere to applicable regulations and ICH guidelines regarding clinical trials, regulatory documents, and safety issues.
- Provide medical consultation to team members and communicate clearly with associates and clients.
- Provide therapeutic and protocol training on assigned studies as requested.
- Assist in writing and/or reviewing safety portions of regulatory documents and reports.
- Perform data reviews as specified in the client contract and data validation manual.
- Medically review adverse event and serious adverse event data from all sources.
Eligibility Criteria for the Remote Pharmacovigilance Job:
- Must be MD or equivalent or MBBS qualified graduate
- 5+ Years of experience in pharmaceutical/biotech industry with at least 2 years in pharmacovigilance/drug safety (global experience is a plus)
- Experience in clinical practice or in academic medicine is a plus
- Working knowledge of relevant pharmacovigilance regulatory requirements and guidance documents
- Demonstrated ability to perform medical assessments of safety data from multiple sources
- Experience with authoring complex documents and contributing to regulatory submissions
- Knowledge of adverse event reporting systems
- Experience in epidemiology, biostatistics, clinical development, or medical affairs is a plus
This is an excellent opportunity for qualified medical professionals to join Thermo Fisher Scientific as a Pharmacovigilance Physician. Interested candidates are encouraged to apply before the deadline to contribute to impactful healthcare solutions.
