Medical Job: Associate Medical Safety Director at IQVIA in Bangalore
Looking for a rewarding medical job in India? IQVIA is hiring an Associate Medical Safety Director in Bengaluru, offering a home-based, full-time role. This position allows medical professionals to contribute to pharmacovigilance, oversee clinical safety data, and support global trials. Explore this opportunity to join one of the top IQVIA careers and make an impact in patient safety.
Job Details:
- Job Title: Assoc Medical Safety Dir
- Location: Bengaluru, India | Full time | Home-based
- Job ID: R1495206
About the Company:
IQVIA is a leading global provider of technology, analytics, and contract research services to the life sciences sector. Recognized for innovative solutions, IQVIA careers offer medical professionals the chance to contribute to healthcare advancements while working with cutting-edge data and technology.
Medical Job – Qualifications:
- Medical degree from an accredited, internationally recognized institution
- Minimum 3 years of clinical practice plus 2 years in pharmaceutical or related industry roles.
- Strong knowledge of clinical trials, safety regulations, and good clinical practice.
- Ability to manage priorities, deadlines, and collaborate with clients and teams.
- Valid medical license or equivalent in the country of residence preferred.
Job Description:
This medical job at IQVIA allows professionals to provide medical expertise in pharmacovigilance, supporting clinical trials and stand-alone safety projects. Responsibilities include reviewing adverse events, post-marketing adverse drug reactions, and ensuring regulatory compliance. The Associate Medical Safety Director plays a key role in maintaining product safety profiles, consulting with internal teams, and contributing to global safety reports. This role is an excellent opportunity within IQVIA careers for those seeking leadership in medical safety.
Medical Job – Key Responsibilities:
- Review and medically evaluate trial-related Adverse Events (AEs) and post-marketing Adverse Drug Reactions (ADRs).
- Compose, edit, and review Analyses of Similar Events (AOSE) based on regulatory requirements.
- Provide guidance to pharmacovigilance case processing teams.
- Conduct aggregate safety reviews to maintain oversight of product safety.
- Review and code clinical data including AEs, medical history, and concomitant medications.
- Represent medical safety findings during client meetings.
- Review and edit IND Annual Reports, EU/US safety reports, and risk management plans.
- Provide oversight for label development, safety monitoring committees, and data safety monitoring board meetings.
- Review project safety and medical monitoring plans, serving as Global Safety Physician or backup as needed.
- Ensure timely medical support for all safety deliverables.
- Stay updated with regulatory and medical-safety industry developments.
