Clinical Medical Manager

at  Novo Nordisk

Clinical Medical Manager
Category: Medical Affairs
Location:Warsaw, Mazowieckie, PL
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!

QUALIFICATIONS

As a Clinical Medical Manager you need to have a Medical Degree or Ph.D in Healthcare with a strong clinical and preferably research background, alternatively Master in Pharmacy or Master of Science with strong, relevant background. In addition, you need to have a minimum of 3 years of Medical Affairsl experience in pharmaceutical industry with strong experience in human clinical trials either from university or the pharmaceutical industry.

To be successful in this role you should have:

• Expertise in therapeutic area of relevance, preferably with authorship in peer-reviewed journals
• Experience as clinical trial investigator or sub-investigator is preferred
• Understanding (or willing to learn) of the specificities and nuances of the local healthcare infrastructure
• Understanding of pharmaceutical drug development Extensive scientific communication skills for internal and external stakeholders, excellent and proactive communication skills, and strong presentation abilities.

Your main 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, map patient journey and treatment pathways and facilitate identification of clinical trial sites, referrals and address educational needs related to New Therapy Areas and clinical trials related to these
• To collect and discuss relevant early development data with external medical and scientific experts optimizing the feasibility process for the clinical trial conduct and provide leadership in the scientific community within New Therapy Areas conducting scientific meetings, engaging with local associations for HCPs on relevant topics.
• To 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.
• To provide timely medical guidance and internal training by supporting training creation and delivering training to clinical staff.
• To engage cross-functionally in scientific communication, transferring knowledge between medical, clinical and commercial functions. The position requires extensive scientific communication internally as well as externally, and excellent and proactive communications skills are a necessity

To be successful in this role you should have:

• Expertise in therapeutic area of relevance, preferably with authorship in peer-reviewed journals
• Experience as clinical trial investigator or sub-investigator is preferred
• Understanding (or willing to learn) of the specificities and nuances of the local healthcare infrastructure
• Understanding of pharmaceutical drug development Extensive scientific communication skills for internal and external stakeholders, excellent and proactive communication skills, and strong presentation abilities