Primary Duties
The Clinical Projects Assistants are responsible for the coordination and tracking of clinical projects (Phases I-IV), maintenance of paper and electronic filing systems, providing support to Clinical Research Associates and Project Managers during the set-up, monitoring and close-down phases of clinical trial sites, the management of the ethics committee applications and the site specific assessment submission process, the coordination of R&D submissions, liaison with suppliers and CROs, and tracking of overall project progress.
Key Attributes/Skills
You will be enthusiastic, with strong interpersonal skills to ensure positive team and customer relationships and have the ability to work both independently and as part of a close-knit team. Strong written and verbal communication skills are required, with excellent working knowledge of MS Outlook, Word, Excel and Power Point. The role is very varied, and requires flexibility, initiative, attention to detail and excellent time management.
Some previous direct relevant experience working as a Clinical Trials Administrator in either a CRO or Pharmaceutical business will be very advantageous, as will a demonstrated knowledge of ICH GCP, but full training can be provided.
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