Clinical Medical Lead
4 tygodni temu
Are you looking for a role where you can leverage your medical expertise to drive scientific discussions and interactions with medical thought leaders? Do you have a strong interest in clinical trials and a passion for improving patients' lives? If so, read on to learn more about this exciting opportunity.
The Role
As a Clinical Medical Manager, you will play a key role in facilitating the execution of clinical trials related to New Therapy Areas, including Cardiovascular, CKD, Liver Diseases, and Alzheimer's diseases. You will provide medical/scientific expertise and advice to support the development of these trials, working closely with key opinion leaders, independent professional associations, and patient advocacy associations.
Key Responsibilities:
- Identify and map key opinion leaders, investigators, and research centers within relevant therapy areas, and collaborate closely with clinical operations teams during feasibility and allocation processes.
- Collect and discuss relevant early development data with external medical and scientific experts to optimize the feasibility process for clinical trial conduct.
- Provide leadership in the scientific community within New Therapy Areas, conducting scientific meetings and engaging with local associations for healthcare professionals on relevant topics.
- Contribute to delivering successful clinical trials (phase I-IV) in collaboration with clinical operations, driving scientific discussions at site selection and initiation visits, and performing ad hoc visits.
- Provide timely medical guidance and internal training by supporting training creation and delivering training to clinical staff.
Requirements
To be successful in this role, you will need a Medical Degree or Ph.D. in Healthcare, with a strong clinical and research background. Alternatively, a Master's in Pharmacy or Master of Science with a strong, relevant background is also acceptable. You will also need a minimum of 3 years of clinical or pharmaceutical industry experience, with a strong background in human healthcare research.
Key Qualifications:
- Expertise in therapeutic areas of relevance, preferably with authorship in peer-reviewed journals.
- Experience as a clinical trial investigator or sub-investigator is preferred.
- Understanding (or willingness to learn) of the specificities and nuances of the local healthcare infrastructure.
- Understanding of pharmaceutical drug development and excellent scientific communication skills for internal and external stakeholders.
About the Department
The Clinical, Medical, and Regulatory (CMR) department at Novo Nordisk is a diverse and collaborative group that drives the development of new treatments for patients with chronic diseases. We provide medical expertise and support for the development of new products, and work closely with healthcare professionals and patients to bring new treatments to market.
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