PHARMAFull-time
Clinical Research Medical Advisor
By Admin · Medical Affairs & MSL
MUMBAI (IN)ONSITEPOSTED: 8/31/2026
PHARMAFull-time
HIRING ORGANIZATIONNOVARTISPharmaceuticals / Healthcare
ROLE DEFINITION & RESPONSIBILITIES
Core Responsibilities
Lead country-level clinical and medical oversight for clinical development programs, ensuring alignment with global strategy and local execution requirements.
Assess clinical trial feasibility by evaluating protocol design, patient population availability, standard of care, and competitive landscape.
Drive study start-up activities including site identification, feasibility validation, and rapid activation timelines.
Provide expert medical guidance to clinical operations teams, investigators, and trial sites.
Support protocol implementation, IRB/EC submissions, informed consent reviews, and regulatory documentation.
Clinical & Scientific Leadership
Act as a key scientific leader engaging with investigators, key opinion leaders (KOLs), regulatory authorities, and patient advocacy groups.
Deliver training on disease areas, study protocols, and investigational products to internal and external stakeholders.
Develop and refine clinical trial strategies addressing recruitment, retention, and data quality risks.
Patient Safety & Compliance
Oversee patient safety by reviewing serious adverse events (SAEs) and supporting pharmacovigilance processes.
Ensure compliance with ICH-GCP, local regulatory guidelines, and global clinical standards.
Participate in audits, inspections, and quality assurance activities.
Cross-Functional Collaboration
Partner with Clinical Development, Medical Affairs, Regulatory, Safety, HEOR, and Patient Access teams.
Contribute to real-world evidence (RWE) initiatives and innovative study designs.
Support alignment between global and local stakeholders for efficient study execution.
Business & Strategic Impact
Influence clinical trial success through improved recruitment strategies and operational efficiency.
Enhance Novartis' scientific reputation through strong investigator relationships and stakeholder engagement.
Accelerate delivery of innovative therapies to patients through optimized clinical execution.
Benefits & Total Rewards
Opportunity to work with a global pharmaceutical leader on cutting-edge clinical programs.
Exposure to advanced clinical development strategies and global trial operations.
Strong internal mobility and leadership development programs.
Collaborative, innovation-driven work culture focused on patient outcomes.
REQUIRED VERIFIED SKILLS
ICH-GCP
Clinical trial feasibility
Protocol development
Clinical research operations
Drug development process
Patient safety
Pharmacovigilance basics
Regulatory compliance
Stakeholder management
Scientific communication
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
For Medical Advisor roles in India, compensation varies widely based on qualifications (MBBS vs MD vs PhD) and company tier. Typical salary ranges from ₹12–30 LPA+, with higher brackets for MD professionals and those with clinical practice background. Companies like Novartis offer performance bonuses, retention incentives, health benefits, and global exposure, significantly enhancing total compensation beyond base salary.
ORGANIZATION CONTEXT & CULTURE
Novartis AG is a Swiss multinational pharmaceutical corporation, one of the largest in the world. It focuses on discovering, developing, manufacturing, and marketing innovative medicines to address significant health needs. The company's portfolio spans various therapeutic areas including oncology, immunology, neuroscience, and cardiovascular diseases.
TEAM SIZE: 76,000+ employees
INDUSTRY: Pharmaceuticals / Healthcare
EXPECTED CAREER ROADMAP
This role sits at the intersection of clinical science and strategic leadership. Candidates typically progress to Senior Medical Advisor, Clinical Development Lead, or Medical Director roles. With experience, professionals can transition into global clinical leadership, therapeutic area head positions, or strategic roles in medical affairs and regulatory strategy. The position builds deep expertise in drug development lifecycle, stakeholder influence, and high-impact decision-making, making it a strong platform for long-term leadership careers in pharma.
APPLICATION ADVISORY
To stand out, emphasize clinical expertise, real-world patient exposure, and understanding of trial design and GCP guidelines. Highlight any involvement in investigator interactions, protocol reviews, or safety reporting. MD candidates should showcase specialization relevance. Be prepared for scenario-based interviews on feasibility assessment, patient recruitment challenges, and SAE handling. Strong communication and stakeholder management examples are critical.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
Verify your capability profile and matching credentials before submitting direct applications.