With 18 years practical experience in roles of increasing responsibility within Clinical Research and Development (CRD) and Medical Affairs (MA) on a regional and global level, Dr. Jürs can support you in all CRD- and MA related questions. In addition to that, Dr. Jürs offers medical consulting services in questions related to health-technology assessments (HTA) and compliance/contractual questions.
Precisely, Dr. Jürs offers medical scientific and strategic consulting regarding:
- Medical scientific strategy (TPP, clinical development, post-registration).
- Medical writing of clinical study documents (CDP, SPs, IB`s, CTDs).
- Complete Medical Affairs portfolio.
- Medical scientific training (e.g. MSLs).
- Compliance training (e.g. sales team) and contract management (e.g. medical).
- Health technology assessments.
- Departmental support (e.g. pharmacovigilance, regulatory, legal, preclinical).
In order to receive a cost-proposal and discuss services please contact Dr. Jürs directly.