With 18 years of 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 with 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.
Besides the services for the pharmaceutical industry, Dr Jürs supports academia in medical writing.
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, IBs, 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).
- Medical writing support of scientific publications.
In order to receive a cost proposal and discuss services, please contact Dr Jürs directly.