Job title:Internal Medical Scientist(novo nordisk)

Qualifications:

• Medical Degree (MD/MBBS); advanced qualifications (PhD, or DM) is preferred and worked with Cardiovascular & Endocrine disorders.

• Proven experience in clinical development of new molecule or scientific roles such as clinician/physician, medical specialist, Principal Investigator/Co-Investigator for Phase 2-3 trials or related industry positions.

Job profile:

The main responsibilities are:

• Contribute to planning and Management of Clinical Development Program: Medical input to clinical development program(s) for phases 2 – 4 as applicable.

• Overall responsible for conduct part of the clinical trials - Clinical Trial Execution & Monitoring -Provide medical oversight during trial conduct of clinical development program, handle medical queries, protocol deviations, and ensure data accuracy through Clinical laboratory surveillance and Medical Monitoring.

• Responsible for medical oversight in delegated projects during execution and drive progress solving in trial-related issues, participate in Medical & Science Teams (MST), safety committees as applicable.

• Contribute with medical input to periodic updates of Investigator’s Brochure and review of medical content of Clinical Trial Reports as applicable

• Medical Device Support -Provide input on risk management, Supporting medical input to medical device technical file documentation and to other medical device development and life-cycle management activities

• Medical Coordination - Act as a liaison between core teams (e.g., Medical Specialists, line managers, GPTs) and ensure alignment with clinical development goals

• Compliance Support to Audit and Inspections - manage medical monitoring audits and support post-audit actions as a Subject Matter Expert (SME).