Clinical Study Consultant (m/f)

Job type:
on-site
Start:
09/16
Duration:
12 MM+
From:
Hays AG
Place:
Hesse
Date:
06/01/2016
Country:
flag_no Germany
project ID:
1139479

Warning
This project is archived and not active any more.
You will find vacant projects in our project database.

We are looking for a
Clinical Study Consultant (m/f)

Reference: 306232/1-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
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Skills:
- Clinical project manager


Keywords: Clinical Project manager