Clinical Medical Manager

7 dni temu


Warszawa, Mazovia, Polska TN Poland Pełny etat

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Clinical Medical Manager - Poland, WarsawClient:Location:

Warsaw, Poland

Job Category:

Other

EU work permit required:

Yes

Job Reference:

98aeb9163027

Job Views:

2

Posted:

15.03.2025

Expiry Date:

29.04.2025

Job Description:

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 be responsible for facilitating the execution of clinical trials related to New Therapy Areas (including Cardiovascular, CKD, Liver Diseases, and Alzheimer's diseases) by providing medical/scientific expertise and advice based on interactions with key opinion leaders (KOLs), independent professional associations, and patient advocacy associations as necessary. In addition, you will be responsible for investigator sites across Poland, where clinical trials in New Therapy Areas are conducted.

Your main responsibilities will be:

  1. 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 processes, map patient journeys and treatment pathways, and facilitate the identification of clinical trial sites, referrals, and address educational needs related to New Therapy Areas and clinical trials related to these.
  2. To collect and discuss relevant early development data with external medical and scientific experts, optimizing the feasibility process for the clinical trial conduct and providing leadership in the scientific community within New Therapy Areas, conducting scientific meetings, and engaging with local associations for HCPs on relevant topics.
  3. 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.
  4. To provide timely medical guidance and internal training by supporting training creation and delivering training to clinical staff.
  5. 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 communication skills are a necessity.

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 a Master in Pharmacy or Master of Science with a strong, relevant background. In addition, you need to have a minimum of 3 years of clinical or pharmaceutical industry experience with strong experience in human healthcare research either from university or the pharmaceutical industry.

To be successful in this role you should have:

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

About The Department

The Clinical, Medical, and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies, providing medical education, collecting data to support real-world experience, and supporting new product development through their life cycle. It provides clinical development, regulatory compliance, and is responsible for medical support of marketed and non-marketed products of high quality.

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