Provide scientific and medical input for early trial planning, start-up, recruitment, and retention.
Monitor trial performance and proactively address scientific issues.
Engage with site staff to ensure compliance and smooth trial conduct.
Act as a local subject matter expert on products and protocols.
Build and maintain relationships with Principal Investigators (PIs) and other key opinion leaders (KOLs).
Communicate pipeline and scientific narratives effectively to internal and external stakeholders.
Contribute to site selection, scientific training, and assessment of medical capabilities.
Introduce Medical Affairs colleagues to KOLs and new therapy areas.
Periodic travel to clinical trial sites within the assigned region and to the India Head Office as required.

Job Requirements

M.B.B.S with M.D. in a relevant discipline with strong clinical practice or research background.
Strong knowledge of ICH-GCP guidelines, regulatory requirements, clinical trial methodology, and pharmaceutical drug development.
Experience in stakeholder engagement and cross-functional collaboration.
Excellent verbal, written, and presentation skills.
Ability to influence internal and external stakeholders.
Innovative, adaptable, and solution-oriented.
Data-driven mindset with willingness to leverage AI and technology tools.

About Company

The Clinical Development Centre-India (CDC-India) is part of the Clinical, Medical, and Regulatory (CMR) department. Clinical Medical Managers play a key role in clinical trial excellence, early portfolio strategy, and scientific leadership with a patient-centered focus.

How to Apply

Submit CV and motivational letter online via the Novo Nordisk career portal.

Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

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