Location: Mumbai, Maharashtra, India
Job Type: Full-Time
Company: IQVIA
Job ID: R1540460
Experience Required: Minimum 9+ years (Not suitable for freshers)
About the Company
IQVIA is a global leader in clinical research services, healthcare analytics, and commercial intelligence for the life sciences industry. The organization plays a pivotal role in accelerating drug development, improving patient outcomes, and enabling data-driven healthcare decisions worldwide.
Job Overview
The Associate Medical Director is a senior-level role responsible for delivering high-quality medical, clinical, and scientific expertise across global clinical trials. This position supports medical monitoring, protocol development, safety evaluation, and stakeholder collaboration throughout the clinical development lifecycle.
The role demands deep therapeutic expertise, strong leadership capabilities, and the ability to act as a global medical advisor for complex clinical research programs.
Key Responsibilities
Medical Monitoring and Scientific Leadership
Serve as Global Medical Advisor for assigned clinical trials and research programs
Provide scientific and medical guidance to Project Leaders and cross-functional teams
Support investigative sites with protocol clarifications, patient eligibility decisions, and safety-related concerns
Ensure medical oversight across all stages of clinical trial execution
Protocol and Clinical Documentation Review
Conduct medical review of study protocols, Investigational Drug Brochures (IDB), and Case Report Forms (CRFs)
Review Clinical Study Reports (CSR) and patient narratives for scientific accuracy and regulatory compliance
Participate in investigator meetings and deliver therapeutic area training
Safety and Pharmacovigilance Collaboration
Review and evaluate Adverse Events (AEs) and Serious Adverse Events (SAEs) in collaboration with Pharmacovigilance teams
Support Analysis of Similar Events (AOSE) and medical coding review
Ensure patient safety and data integrity across clinical studies
Stakeholder and Project Engagement
Participate in kick-off meetings, sponsor discussions, and internal project reviews
Act as a key medical interface between sponsors, CRO teams, and investigative sites
Provide medical input to business development and proposal strategies
Operational Excellence
Ensure adherence to global regulatory standards including ICH-GCP and local compliance guidelines
Be available for urgent medical queries related to ongoing trials
Support audit readiness and quality assurance processes
Required Qualifications
Medical Degree (MD or equivalent) from a recognized institution
Specialty Board Certification (preferred), especially in Oncology
Minimum 5 years of clinical practice experience plus 4+ years in clinical trials (Pharma, CRO, or Biotech industry)
Strong expertise in medical monitoring, clinical trial design, and safety evaluation
In-depth understanding of global regulatory requirements and clinical research guidelines
Excellent communication, leadership, and decision-making skills
Preferred Candidate Profile
Medical Oncologist or therapeutic area specialist (highly preferred)
Experience working on global, multi-center clinical trials
Strong exposure to pharmacovigilance processes and safety data review
Ability to manage complex clinical programs and cross-functional stakeholders
Why This Role Stands Out
Opportunity to lead global clinical trials and high-impact drug development programs
Work within a globally recognized CRO with strong industry credibility
Exposure to advanced clinical research methodologies and innovative therapies
Career growth into Medical Director and leadership roles
Important Note for Applicants
This is a senior-level position requiring extensive experience in clinical medicine and clinical research. Freshers or early-career professionals are not eligible for this role. Candidates seeking entry into the pharmaceutical industry should explore roles such as Drug Safety Associate, Clinical Research Coordinator, or Medical Writer.
How to Apply
Apply directly through the official careers portal of IQVIA or explore verified global job opportunities on ThePharmaDaily.com.
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Remote, India | Siliguri |Illinois :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
Arizona | Buffalo Grove | Clayton | Downers Grove | fairmont | Georgia | Keene | Michigan | Mt. Pleasant | New Jersy | OH | Piedmont | Salisbury | United States | Whitesboro | Winston-Salem |Georgia :
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Copenhagen | Denmark |Europe :
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Sheffield |Oxfordshire :
Witney |Ontario :
Richmond Hill | Uxbridge | Renfrew | Australia | Mississauga | North York |Canada :
Canada |Quebec :
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Zaventem |South America :
Argentina | Peru |Brazil :
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Croatia |Zagreb :
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Niš |Bohemia :
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Santiago |Bosnia and Herzegovina :
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