Description
We are looking for a
Clinical Study Consultant (m/f)
Reference: -en
Start: 09/16
Duration: 12 MM+
Place: in Hesse
Branch: Wettbewerber
Your tasks:
- Deliver scientific expertise in oncological projects (development strategies, study designs, publications, answer medical questions)
- Provide expert review of clinical documents, review of literature and publication including written feedback reports
- Provide expert up-to-date knowledge of oncology, international regulations, guidelines and requirements for global drug development, medical information and marketing
- Provide medical writing services for clinical study protocols and clinical study reports
- Responsibility for reviewing and finalising clinical study documents (study protocol, CRF, patient information and informed consent)
- Support submissions to regulatory authorities and ethics committees
Your qualifications
- Medical affairs background
- Business fluent English skills
- Profound GCP expertise, medical writing expertise, expertise with regard to oncology project s
Skills:
- Clinical project manager
Keywords: Clinical Project manager