Key job skills:
•A thorough understanding of clinical trial design, trial monitoring practices and all aspects of the drug development process is essential
•Medical scientific writing skills
•A thorough knowledge of ICH/GCP guidelines and their impact on all areas of the clinical research process.
•Trial Management or Field monitoring experience is an advantage
•Experience in activities related to interim analysis and data base lock e.g. data cleaning
•Ability to coordinate CROs

Your profile:
•A life sciences degree
•At least 2-3 years experience in the clinical environment
•Must have the ability to work independently and collaboratively on a project
•Effective oral and written communication skills

Great daily rates and possibility of extension to 12 months for the right candidate.