Clinical Medical Advisor

Clinical Medical Advisor

**Category**:Project Management & Agile**Location**:Puteaux, Île-de-France, FR-
**The position**
- As
- **Clinical Medical Advisor**, you will facilitate the execution of Global Clinical Trials related to Cardiovascular and kidney disorders, Liver Disease, and Alzheimer's disease (Novo Nordisk New Therapy Areas) by providing medical/scientific expertise and advice based on interactions with KOLs, independent professional associations and patient advocacy associations as necessary.- Some of your responsibilities will be to:- Identify and map KOLs, investigators and research centres within the relevant therapy areas and collaborate closely with clinical operations teams during feasibility and allocation process.
- Collect and discuss relevant early development data with external medical and scientific experts optimizing the clinical trial execution and provide leadership in the scientific community within the relevant Therapy Areas conducting advisory boards, scientific meetings, engaging with local associations for HCPs on relevant topics.
- Contribute to delivering successful clinical trials (phase I-IV) in collaboration with clinical operations including driving scientific discussions at site selection and initiation visits, performing ad hoc visits, supporting attendance at investigator meetings, ensuring KOL inclusion in clinical trials, and engaging key investigators to communicate trial results.
- Provide scientific and medical responses to internal and external stakeholders and deliver training to clinical staff on the scientific background of the trial.**Qualifications**
- We are searching for Medical Doctors with solid clinical experience OR pharmaceutical industry professionals with minimum 3 years of experience in Medical Affairs who have had exposure to clinical trials:- MD or PhD in healthcare with strong clinical and preferably research background, alternatively Pharmacist or Master of Science with strong, relevant background.
- Good understanding of drug development processes and the specificities and nuances of the local healthcare infrastructure.
- Expertise in Metabolic and Cardiovascular diseases, Nephrology, Hepatology (NASH), or CNS (Alzheimer’s disease).
- Experience as clinical trial investigator or sub-investigator is preferred.
- Fluent French in addition to advanced English verbal and writing skills.- As a person you are open and communicative, with strong presentation skills and a can-do attitude. You are independent and show initiative when planning and performing tasks assigned either by management or by yourself. You are open to travel frequently (30% of your time) to visit sites, attend congresses and company events.**About the department**
- You will become a part of a Clinical Medical Regulatory (CMR) department counting 60 colleagues covering France. Within the department, you will be closely working with the Head of the clinical team.- Your direct team members are 3 other Clinical Medical Advisors, all reporting to a Team Lead who is reporting to the VP CMR France.- French affiliate of Novo Nordisk belongs to Region North West Europe (NWE).**Working at Novo Nordisk**
- At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales - we’re all working to move the needle on patient care.**Contact**Deadline**- We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.- At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.