Beschreibung
Responsibilities:- Management of CDM activities of clinical trials (1-2 trials , phase II-III, pain indication)
- Set up of clinical trials in cooperation with CROs (Medidata Rave)
- Managing conduct of CDM activities in CTs
- Oversee and supervision of CROs and other external vendors
- Quality control measures
- Process compliance
- Issue management
o Represent CDM in internal study team
o Organize and manage trial filing activities
o Oversee CDM part of the trial budget
Requirements
- At least 5 years of experience in managing CDM activities in CTs
- Hands on experience in overseeing CDM activities of CROs and other external data providers
- excellent negotiation and communication skills
- excellent team player capabilities
- Good English skills
If you are interested call me a.s.a.p. or send your CV in WORD format.
Also if you know somebody who would be interested in this position, then please contact me.
Warm regards,
Carla Störzer