- Location:
- Athens, Attica, Greece
- Salary:
- Competitive
- Type:
- Permanent
- Main Industry:
- Search Health, Nursing & Social Services Jobs
- Other Industries & Skills:
- Legal
- Job ID:
- 130278258
- Posted On:
- 28 March 2024
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 role is based in Athens, Greece and reports to the Clinical Medical Manager Lead.
The position
As Clinical Medical Manager, you will be part of medical affairs and clinical operations teams within the affiliate, whilst collaborating closely with relevant stakeholders in clinical development, trial planning and development, globally. You will facilitate execution of clinical trials related to New Therapy Areas (including CVD, NASH, 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. Your area of responsibility will be all areas in Greece, where clinical trials in the above Therapeutic Areas are conducted.
Your Main Responsibilities will Be:
style=”margin-bottom:13.0px”-
-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 advisory boards, scientific meetings, engaging with local associations for HCPs on relevant topics.
-To contribute to delivering successful clinical trials (phase II-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 KOLs 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.
As a person you are a charismatic communicator 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 international travel to visit sites, attend congresses and company events.
Qualifications
We are searching for Medical Doctors with clinical experience or pharmaceutical industry professionals with minimum 3 years of experience in Medical Affairs:
-MD or PhD in healthcare with a clinical and/or research background. Other educational backgrounds could be considered if in combination with strong experience.
-Good understanding of drug development processes and the specificities and nuances of the local healthcare infrastructure.
-Expertise in Cardiovascular disease, NASH or Alzheimer will be an advantage.
-Fluent English & Greek verbal and writing skills.
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
Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 60,000 employees. Together, we go further. Together, we’re life changing.
Contact
Please submit your application via the Novo Nordisk website. We are unable to accept direct CVs.
Deadline
Apply before the 4th of March 2024
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.
To help us track our recruitment effort, please indicate in your email/cover letter where (vacanciesin.eu) you saw this job posting.
