Pharmacovigilance Job at IQVIA | Apply Now for the Operations Specialist Role
IQVIA, a global leader in clinical research services and healthcare intelligence, is hiring an Operations Specialist 1 in Thāne, India. This Pharmacovigilance Job is ideal for candidates with a background in life sciences or healthcare looking to advance their career in pharmacovigilance and safety data operations. Join IQVIA to contribute to patient safety and regulatory compliance while gaining exposure to international projects.
About The Company
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence. The organization connects advanced analytics with deep scientific expertise to accelerate the development and commercialization of innovative medical treatments, improving patient outcomes worldwide.
Job Overview:
As an Operations Specialist 1 at IQVIA, you will review, assess, and process safety data across multiple service lines. You will work with internal teams and external stakeholders to ensure accurate, timely, and compliant distribution of safety reports. This role provides hands-on experience in adverse event case processing, coding, literature review, and database management.
Key Responsibilities:
- Review and process Adverse Events (AE) and endpoint data according to SOPs and regulatory guidelines.
- Perform data entry, coding of AE and products, and narrative writing.
- Conduct literature screening and manage pharmacovigilance database tasks.
- Maintain high-quality standards and ensure timely case delivery.
- Collaborate with project teams, healthcare professionals, and clients on safety data matters.
- Assist in mentoring new team members as assigned.
- Participate in team meetings and provide feedback on operational challenges and improvements.
- May perform medical review of non-serious AE/ADR, including coding, causality assessment, and completeness checks.
- Ensure compliance with global, regional, and local regulations in all assigned tasks.
Qualifications for the IQVIA Job:
- Education: Bachelor’s degree in Life Sciences or related field (or High School Diploma with scientific/healthcare background).
- Experience: Up to 3 years relevant experience; up to 1 year in pharmacovigilance preferred.
- Knowledge of medical terminology and safety databases.
- Understanding of global, regional, and local clinical research regulatory requirements.
Skills & Abilities:
- Strong attention to detail and organizational skills.
- Excellent verbal and written communication skills.
- Ability to work independently and in a team environment.
- Flexibility to manage multiple tasks, meet deadlines, and adapt to process changes.
- Willingness to learn new skills across safety service lines.
- Familiarity with Microsoft Office and web-based applications.
- Shift flexibility and occasional travel may be required.
Why Join IQVIA:
- Gain exposure to global pharmacovigilance projects.
- Learn from experienced professionals in a dynamic work environment.
- Contribute to patient safety and regulatory compliance initiatives.
- Opportunity for career growth in clinical operations, safety, and regulatory affairs
