Medical Advisor Job at IQVIA in Bengaluru | Medical Graduates Apply
This medical advisor job at IQVIA presents a senior-level opportunity for professionals specializing in pharmacovigilance and drug safety. Based in Bengaluru, this role focuses on evaluating safety data, supporting global regulatory compliance, and strengthening patient safety outcomes. Ideal for experienced professionals exploring IQVIA careers, this position is well-suited for those seeking impactful medical jobs in Bangalore and jobs in Bengaluru.
Job Details:
- Job Position: Senior Medical Safety Advisor
- Location: Bengaluru, India (Home-based)
- Job ID: R1523538
About the Company
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The organization creates intelligent connections to accelerate the development and commercialization of innovative medical treatments, helping to improve patient outcomes and population health worldwide. This IQVIA job reflects the company’s commitment to integrity, scientific excellence, and global healthcare advancement, making IQVIA careers highly sought after within the life sciences sector.
Job Description
This medical advisor job at IQVIA involves providing medical expertise in pharmacovigilance and drug safety activities. The role focuses on reviewing adverse event data, evaluating safety signals, supporting regulatory reporting, and maintaining oversight of product safety profiles. Based in Bengaluru, this opportunity is ideal for experienced professionals seeking senior-level medical jobs in Bangalore within IQVIA careers.
Qualifications
- Other A medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education. Req
- 3 years of experience practicing clinical medicine after the award of a medical degree. Graduate, and/or Residency training can qualify for clinical practice experience Req
- Two (2) years of pharma experience Pref
- Sound knowledge of Medicine
- In-depth knowledge of applicable global, regional, and local clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Knowledge of Pharmacovigilance- ICSR and Aggregate reports
- In-depth knowledge of departmental standard operating procedures (SOPs)
- Skill in the use of multiple safety databases
- Adequate Computer skills, especially Microsoft word, excel & PowerPoint
- Good communication skills- verbal and written
- Ability to establish and maintain effective working relationships with managers, co-workers, investigative site staff, clients, and regulatory agency representatives
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients
- A valid medical license, or equivalent, from the country or region in which he/she resides and works Pref
Key Responsibilities
- Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs), including narrative content, queries, coding, expectedness, seriousness, causality, and company summary
- Compose, edit, and medically review Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulatory requirements
- Provide coding review of AEs, SAEs, SADRs, Past medical history, Concomitant medications, or other medical data listings to verify and medically vet clinical data
- Serve as an internal consultant to pharmacovigilance case processing teams on projects being supported
- Perform medical safety review of the protocol, Investigative Brochure, and/or Case Report Forms (CRFs) for appropriate safety content and data capture, as applicable
- Provide aggregate reviews of safety information, including but not limited to clinical data, postmarketing, literature review, and observational studies to maintain oversight of a product’s safety profile (e.g, DSUR, RMP, PBRER, ad hoc regulatory reports, etc)
- Ensure service delivery from a productivity, compliance, and quality perspective within regulatory /contracted timelines. Lead and participate in the initiatives taken for the same from a team delivery perspective
- Provide therapeutic area/pharmacovigilance issue guidance in the context of leading/managing other safety team members in a single case assessment
- Ensure update of watch list, list of expected tasks, labeling list/RSIs, etc., for the assigned products, and develop such additional capabilities within the team
- Lead, drive, and participate in training activities, product transitions, audit preparation, and knowledge exchange initiatives
- Review and sign off on the Project Safety Plan and Medical Monitoring Plan per the medical safety scope agreed in the contract, as applicable
- Attend project meetings, medical safety team meetings, and represent safety and clinical data review findings during client meetings, as applicable
- Act as Lead Safety Physician, or additional team support, and/or back up on assigned projects as applicable
- Provide medical escalation support for medical information and EU Qualified Persons for Pharmacovigilance projects, as applicable
- 24-hour medical support as required on assigned projects
- Maintain awareness of medical safety-regulatory industry developments
- Provide support and participate in signal detection efforts, e.g., strategy meetings, etc., as applicable
