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International Medical Affairs Manager (Oncology) (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Marketing, Support
Projektbeschreibung
- Support of the implementation of the global strategic medical affairs plan, by working closely together with the international business team and medical team
- Medical management of 3 clinical trials currently in a different stage
- Provide input into study documents such as medical monitoring plans, SAP, CRFs, writing protocols and preparing amendments
- Oversee the management of protocol violations
- Supervise CRO & coordinate activities of different external vendors to ensure tasks are delivered on time and with good quality
- Be the link between the business team, study management team, biomaker team, operations department and affiliates involved in the study
- Ensure that data are delivered on time and with good quality for publication at congresses
- Leading member of the clinical trials review team, reviewing phase IV trial-synopses for medical-scientific correctness and strategic fit
- Responsible for the review and content of internal publication alerts and marketing material
- Cross-functional team work in order to organize an oncology global medical advisory board and other RA global expert meetings
- Liaise with affiliates
- Involved in the coordination of global phase IV clinical trial programme and writing of draft synopsis
- The position involves about 35% travelling in Europe to the affiliates (Monza, London, Paris, etc.) and USA (San Francisco) and travelling to congresses where you will be in contact with KOLs
- Experience in communicating medical-scientific information on an internal and external international level
- In-depth experience in pharma environment (Clinical or Pharma Sponsor)
- MD or PhD in Life Sciences preferred
- Experience in Oncology/familiarity with data queries in oncology preferred
- Good communication style
- Strong in analysing
- Post marketing experience
Weitere Qualifikationen: Medical affairs manager
- Medical management of 3 clinical trials currently in a different stage
- Provide input into study documents such as medical monitoring plans, SAP, CRFs, writing protocols and preparing amendments
- Oversee the management of protocol violations
- Supervise CRO & coordinate activities of different external vendors to ensure tasks are delivered on time and with good quality
- Be the link between the business team, study management team, biomaker team, operations department and affiliates involved in the study
- Ensure that data are delivered on time and with good quality for publication at congresses
- Leading member of the clinical trials review team, reviewing phase IV trial-synopses for medical-scientific correctness and strategic fit
- Responsible for the review and content of internal publication alerts and marketing material
- Cross-functional team work in order to organize an oncology global medical advisory board and other RA global expert meetings
- Liaise with affiliates
- Involved in the coordination of global phase IV clinical trial programme and writing of draft synopsis
- The position involves about 35% travelling in Europe to the affiliates (Monza, London, Paris, etc.) and USA (San Francisco) and travelling to congresses where you will be in contact with KOLs
- Experience in communicating medical-scientific information on an internal and external international level
- In-depth experience in pharma environment (Clinical or Pharma Sponsor)
- MD or PhD in Life Sciences preferred
- Experience in Oncology/familiarity with data queries in oncology preferred
- Good communication style
- Strong in analysing
- Post marketing experience
Weitere Qualifikationen: Medical affairs manager
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Marketing/Vertrieb, Sonstiges