Job Description Summary

Job Description

Key Responsibilities

• Build and maintain scientific partnerships with Medical Experts (MEs), Key Opinion Leaders (KOLs), and key healthcare accounts through meaningful medical and scientific engagements.
• Develop and execute strategic ME engagement plans aligned with organizational and therapeutic area priorities.
• Respond to unsolicited medical and scientific information requests, ensuring accurate, balanced, and compliant communication.
• Support the planning and execution of clinical research activities, including collaboration with study sites and clinical operations teams.
• Facilitate Investigator Initiated Trials (IITs) by providing scientific support and guidance to investigators as per company processes.
• Act as a trusted medical resource for internal cross-functional teams, providing scientific insights and therapeutic expertise.
• Ensure timely reporting of adverse events, product quality complaints, and special situation cases in accordance with pharmacovigilance and compliance requirements.
• Support medical education initiatives and scientific exchange activities to enhance disease and product awareness.

Essential Requirements

• Education: Any Graduate (Life Sciences, Pharmacy, Biotechnology, Medicine, or related healthcare disciplines preferred).
• Experience: 3-8 years of experience in Medical Affairs, Medical Science Liaison (MSL), Clinical Research, Scientific Engagement, Healthcare Consulting, or related pharmaceutical/healthcare roles.
• Strong understanding of medical and scientific communication principles.
• Experience engaging with healthcare professionals, medical experts, or key stakeholders within the healthcare ecosystem.
• Knowledge of clinical research processes, evidence generation, and medical compliance requirements.
• Excellent stakeholder management, presentation, influencing, and communication skills.
• Ability to interpret and communicate complex scientific and clinical data.

Desirable Requirements

• Experience in an MSL, Medical Advisor, Clinical Research, or Medical Affairs role within the pharmaceutical or healthcare industry.
• Exposure to Investigator Initiated Trials (IITs), clinical studies, or evidence generation projects.
• Understanding of pharmacovigilance, adverse event reporting, and healthcare compliance standards.
• Advanced degree or certification in Life Sciences, Pharmacy, Clinical Research, or related disciplines.
• Experience working in cross-functional and matrix organizations.

Key Performance Indicators (KPIs)

• Achievement of annual ME engagement and medical activity targets.
• Quality and effectiveness of scientific engagements with Medical Experts and key stakeholders.
• Timely and compliant response to medical information requests.
• Successful support and execution of clinical research and IIT activities.
• 100% adherence to Ethics, Compliance, and Pharmacovigilance requirements.
• Timely reporting of adverse events, technical complaints, and special situation cases.

Skills Desired