Consultant Clinical Regulatory Affairs & Study Start-Up

Over 17 years experience in Regulatory Affairs and Study Start-Up in the Clinical Trials environment.
Regulatory Project Lead in local, European and global phase I-IV CNS, oncology, dermatology, respiratory diseases, in adult and pediatric studies.

• Good clinical practice (GCP)
• Klinische Studie
• Pharmaforschung
• Regulatory Affairs Management

Over 17 years experience in Regulatory Affairs and Study Start-Up in the Clinical Trials environment.
Regulatory Project Lead in local, European and global phase I-IV CNS, oncology, dermatology, respiratory diseases in adult and pediatric studies.
Vast knowledge in clinical trial submissions and life-cycle in Europe (espacially DACH-region and Poland).
Speaking German, English and Polish fluently.

Looking for freelance opportunity in the clinical trials environment in Rhine-Main region or remotely.