Medical Advisor | Clinical Trials & Medical Affairs | Mumbai | Abbott
Company: Abbott
Location: Mumbai, India
Job Type: Full-Time
Work Mode: On-site
Experience: 1+ Year (Early to Mid-Level)
Job Overview
Abbott is looking for a Medical Advisor to support clinical research, medical affairs strategy, and safety monitoring across product development. This role is ideal for professionals aiming to build expertise in clinical trials (Phase III & IV), pharmacovigilance, and regulatory reporting.
As a Medical Advisor, you will play a key role in clinical trial execution, investigator engagement, and data-driven decision-making, contributing directly to the development and lifecycle management of pharmaceutical products.
Key Responsibilities
Clinical Trials & Research Execution
Oversee planning, execution, and monitoring of clinical trials (Phase III & IV)
Support implementation of clinical protocols and study designs
Ensure timely completion of studies and final reports
Investigator & Study Management
Recruit and engage clinical investigators and research sites
Coordinate investigator meetings and study initiation activities
Negotiate study design parameters and associated costs
Regulatory & Compliance Support
Prepare and coordinate reports for regulatory submissions
Ensure adherence to ICH-GCP guidelines and clinical protocols
Monitor study compliance and audit readiness
Pharmacovigilance & Safety Monitoring
Participate in adverse event (AE) and safety reporting
Support pharmacovigilance activities and safety signal tracking
Ensure compliance with global safety reporting standards
Data Management & Reporting
Facilitate data collection and clinical documentation processes
Contribute to study analysis and reporting outcomes
Support regulatory and internal stakeholders with clinical data
Cross-Functional Collaboration
Act as liaison with internal teams and external partners
Collaborate with regulatory, clinical operations, and medical teams
Support partnerships under licensing or co-development agreements
Required Skills & Qualifications
Educational Qualification
Associate Degree (or higher) in Life Sciences / Pharmacy / Medical-related field
Experience
Minimum 1 year of experience in Medical Affairs / Clinical Research / Pharma Industry
Technical Skills
Understanding of clinical trial phases (III & IV)
Knowledge of ICH-GCP, regulatory requirements, and clinical protocols
Familiarity with pharmacovigilance (PV) and adverse event reporting
Basic exposure to clinical data management and regulatory submissions
Core Competencies
Strong analytical and problem-solving skills
Effective communication and stakeholder coordination
Ability to work independently with minimal supervision
Attention to detail and compliance-driven mindset
Perks & Benefits
Opportunity to work with a leading global pharmaceutical company
Hands-on experience in clinical trials and drug development lifecycle
Career growth in Medical Affairs, Clinical Research, and Pharmacovigilance
Exposure to cross-functional global teams and projects
Learning and development opportunities in advanced therapeutic areas
Compensation
Salary Range: Not disclosed (competitive as per industry standards)
About the Company
Abbott is a globally recognized healthcare leader specializing in pharmaceuticals, diagnostics, nutrition, and medical devices. The company is committed to advancing healthcare through innovation, clinical research, and patient-centric solutions.
Why This Role is High-Value
This role is ideal for professionals looking to grow in:
Medical Affairs & Clinical Strategy
Clinical Trials & Drug Development
Pharmacovigilance & Drug Safety
Regulatory Affairs & Compliance
Healthcare Research & Data Analysis
Application Process
Apply through Abbott’s official careers portal.
Call to Action
If you want to break into high-impact clinical research and medical affairs, this role gives you direct exposure to real clinical trials, regulatory strategy, and patient safety systems.
Start building your authority in pharma, clinical development, and global healthcare innovation.
Apply now and take your first serious step into the pharma industry. 🚀
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