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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 to facilitate 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 investigators sites across Poland, where clinical trials in New Therapy Areas are conducted.

The position offers remote flexibility, so we are open to candidates located in the following cities: Warsaw, Wrocław, Gdańsk, Poznań and Lublin.

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 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.
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 provide leadership in the scientific community within New Therapy Areas conducting scientific meetings, 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 communications 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 Master in Pharmacy or Master of Science with strong, relevant background. In addition, you need to have a minimum of 3 years of Medical Affairs 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:

1. Expertise in therapeutic area of relevance, preferably with authorship in peer-reviewed journals.
2. Experience as clinical trial investigator or sub-investigator is preferred.
3. Understanding (or willing to learn) of the specificities and nuances of the local healthcare infrastructure.
4. Understanding of pharmaceutical drug development.
5. 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 support new product development through their life cycle. It provides clinical development, regulatory compliance, and it is responsible for medical support of marketed and non-marketed products of high quality.

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 to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.

Contact

Please apply with your CV via the online recruitment system.

We thank all applicants for their interest, however, only those candidates selected for interviews will be contacted.

Deadline

Please apply before 17 th of February 2025.

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.

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