PV Coordinator Jobs – FSP
A rare chance for aspiring professionals in pharmacovigilance! Thermo Fisher is offering PV Coordinator jobs in Hyderabad, Andhra Pradesh. This full-time role focuses on serious and non-serious adverse events, providing an excellent opportunity for candidates with a background in life sciences.
About the Company
The hiring organisation is a prominent global contract research organisation (CRO) specialising in clinical research services. With a commitment to advancing healthcare, they support top pharmaceutical companies and biotechs in bringing innovative therapies to market. Their clinical research team is dedicated to addressing the world’s most challenging health concerns through scientific and clinical expertise.
Job Details:
- Location: Hyderabad, Andhra Pradesh, India
- Job ID: R-01362187
- Job Type: Full-time
- Category: Clinical Research
- Remote: Fully Remote
- Work Schedule: Standard (Mon-Fri)
- Environmental Conditions: Office
Job Description
Join as a PV Coordinator and make an impact at the forefront of innovation. The organisation has successfully supported the top 50 pharmaceutical companies and over 750 biotechs, spanning 2,700 clinical trials across more than 100 countries in the last five years. In this PV Coordinator role, you will provide contracted project coordination and safety support on global and domestic programs.
Responsibilities include:
- Coordinating the timely review of protocol inquiries, serious and non-serious adverse events, and Data Safety Monitoring Board data.
- Representing the organisation’s DSMB/EAC Coordination Team at global and domestic committee meetings.
- Preparing Confidentiality Disclosure Agreements, Letters of Intent, and Member Agreements based on contractual considerations.
- Compiling adjudication dossiers and creating/submitting follow-ups to investigative sites.
- Managing project-specific training and ensuring audit readiness.
- Performing data entry into internal/external databases and managing project expenses.
- Providing training to junior staff.
Eligibility Criteria
- Graduation in any Life Science degree is preferred.
- 1+ Years of experience in Pharmacovigilance Case processing is required.
- Experience in Argus database is advantageous.
Required Skills
- Strong problem-solving skills.
- Ability to work independently with minimal supervision.
- Excellent communication and interpersonal skills.
- Strong attention to detail and accuracy.
- Flexibility to reprioritise workload to meet changing project timelines.
Why Join
Working with this organisation provides a unique opportunity to contribute to significant advancements in healthcare. The role of a PV Coordinator is essential in ensuring the safety and efficacy of clinical trials, making a tangible impact on patient health outcomes. The collaborative environment fosters professional growth and development, making it an ideal workplace for those passionate about life sciences and pharmacovigilance.
The PV Coordinator jobs at this leading global contract research organisation represent a significant opportunity for professionals in the field of pharmacovigilance. With a focus on serious and non-serious adverse events, this role is perfect for candidates looking to advance their careers in life sciences. Interested individuals are encouraged to apply before the deadline to seize this chance to make a meaningful impact in healthcare.
