Clinical Medical Manager
il y a 3 semaines
Are you looking for an opportunity where you can utilize your medical knowledge to communicate scientific data and to interact with medical thought leaders? Are you passionate about the world of clinical trials? Are you highly motivated by being able to make a difference to improving patients’ lives? If so, you should continue reading and apply today
The position
As Clinical Medical Manager, you will facilitate the execution of Global Clinical Trials related to Novo Nordisk New Therapy Areas including but not limited to Cardiometabolic and kidney disorders, Liver Disease, and Alzheimer's disease 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 experience in clinical research and / OR pharmaceutical industry professionals with minimum 3 years of experience in Medical Affairs or R&D department :
MD or PharmD with clinical and preferably research background.
Good understanding of drug development processes and the specificities and nuances of the local healthcare infrastructure.
Expertise in Cardiometabolic diseases, Cardiology or Nephrology.
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 (20% 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 70 colleagues covering France. Within the department, you will be closely working with the Head of the clinical team.
Your direct team members are 4 other Clinical Medical Managers (CMM), all reporting to a CMM Lead who is reporting to the VP CMR France.
French affiliate of Novo Nordisk belongs to Region North West Europe (NWE).
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