Remote Non-Clinical Job at IQVIA, Thane
Looking for a high-level career in pharmacovigilance and drug safety? IQVIA is hiring an Associate Medical Safety Director for a full-time, home-based role in India. This Remote Non-Clinical Job position at IQVIA Careers focuses on providing medical expertise in pharmacovigilance and clinical safety. Candidates will be involved in safety monitoring, regulatory reporting, and clinical trial oversight. The Job in Thane offers an opportunity to work on global projects and collaborate with international teams. It is ideal for experienced professionals in clinical research and drug safety.
About IQVIA:
IQVIA is a leading global provider of clinical research services, healthcare intelligence, and commercial insights. The company supports the life sciences industry by accelerating the development and commercialization of innovative medical treatments. IQVIA is known for its data-driven approach and commitment to improving patient outcomes worldwide.
Job Details:
- Job Title: Associate Medical Safety Director
- Location: Thane, India (Home-based)
- Job Type: Full-time
- Job ID: R1532084
- Industry: Clinical Research / Pharmacovigilance
Key Responsibilities:
- Perform medical review of adverse events (AEs) and adverse drug reactions (ADRs) in this Remote Non-Clinical Job
- Conduct safety assessments, including causality, seriousness, and expectedness
- Review and prepare regulatory safety reports and documents
- Provide aggregate safety data analysis and oversight
- Support pharmacovigilance teams as a medical consultant in this Remote Non-Clinical Job at IQVIA Careers
- Participate in safety monitoring committees and board meetings
- Contribute to risk management plans and safety strategies
- Review clinical trial protocols and safety-related documents in this Job in Thane
- Ensure compliance with regulatory guidelines and timelines
- Provide 24-hour medical support for assigned projects
Educational Requirements for this Job:
- Medical degree from a recognized institution
- Minimum 3 years of clinical practice experience
- An additional 2 years of experience in the pharmaceutical or related industry
- Valid medical license (preferred)
Skills Required:
- Strong knowledge of pharmacovigilance and drug safety
- Understanding of clinical trials and research processes
- Knowledge of regulatory guidelines and GCP
- Analytical and decision-making skills
- Ability to manage multiple projects and deadlines
- Strong communication and stakeholder management skills
- Flexibility and problem-solving ability
Benefits of the Remote Non-Clinical Job:
- Work-from-home flexibility
- Opportunity to work with a global leader in clinical research
- Exposure to international pharmacovigilance projects
- Career growth in drug safety and regulatory domains
- Collaborative and professional work environment
- Contribution to global healthcare and patient safety
