Medical Advisor | Clinical Trials & Medical Affairs | Mumbai
Company: Abbott
Location: Mumbai, India
Job Type: Full-Time
Work Mode: On-site
Experience: 1+ Years
Job Overview
Abbott is hiring a Medical Advisor to support clinical research, medical affairs strategy, and regulatory compliance. This role is ideal for professionals looking to gain hands-on experience in clinical trials (Phase III & IV), pharmacovigilance, and healthcare data analysis.
As a Medical Advisor, you will work closely with clinical teams, investigators, and regulatory bodies to ensure successful execution of clinical studies and adherence to global standards like ICH-GCP.
Key Responsibilities
Clinical Trials & Research Management
Oversee planning, execution, and monitoring of clinical trials (Phase III & IV)
Support implementation of clinical protocols and study designs
Ensure completion of studies and preparation of final reports
Investigator & Site Management
Recruit and coordinate with clinical investigators and research sites
Manage investigator meetings and study initiation activities
Negotiate study design parameters and associated costs
Regulatory & Compliance
Prepare and coordinate documentation for regulatory submissions
Ensure adherence to ICH-GCP guidelines and study protocols
Monitor compliance and determine study completion readiness
Pharmacovigilance & Safety
Participate in adverse event (AE) reporting and safety monitoring
Support pharmacovigilance processes and regulatory safety requirements
Data Collection & Reporting
Oversee clinical data collection and documentation
Provide reporting support for submissions to regulatory authorities
Ensure accuracy and completeness of study-related data
Cross-Functional Collaboration
Coordinate with internal medical, regulatory, and clinical teams
Act as liaison with external partners under licensing agreements
Support collaborative research and development initiatives
Required Skills & Qualifications
Educational Qualification
Associate Degree or higher in Life Sciences / Pharmacy / Medical field
Experience
Minimum 1+ year experience in Medical Affairs / Clinical Research / Pharma Industry
Technical Skills
Knowledge of clinical trial phases (III & IV)
Understanding of ICH-GCP, regulatory requirements, and SOPs
Familiarity with pharmacovigilance (PV) and adverse event reporting
Exposure to clinical data management and regulatory documentation
Core Competencies
Strong analytical and problem-solving skills
Effective communication and stakeholder management
Ability to work independently with minimal supervision
High attention to detail and compliance-focused mindset
Perks & Benefits
Work with a top global pharmaceutical company
Hands-on experience in clinical trials and drug development lifecycle
Growth opportunities in Medical Affairs, Clinical Research, and Regulatory Affairs
Exposure to global standards and cross-functional collaboration
Learning and development in therapeutic and clinical domains
Compensation
Salary Range: Not disclosed (competitive as per industry standards)
About the Company
Abbott is a leading global healthcare organization specializing in pharmaceuticals, diagnostics, medical devices, and nutrition products. The company is committed to advancing healthcare through innovation, clinical excellence, and patient-focused solutions.
Why This Role is High-Value
This role is ideal for professionals aiming to build careers in:
Medical Affairs & Clinical Strategy
Clinical Trials & Drug Development
Pharmacovigilance & Drug Safety
Regulatory Affairs & Compliance
Healthcare Research & Data Analysis
Application Process
Apply through the official Abbott careers portal.
Call to Action
If you want to enter the core engine of drug development—clinical trials and medical affairs—this is your entry point.
Build real expertise, work on live clinical studies, and position yourself for high-growth roles in pharma.
Apply now and start your journey into the pharmaceutical industry. 🚀
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