Profile:
The Clinical Research Associate will be responsible for monitoring clinical trial sites to ensure compliance with the protocol, with GCP and with other appropriate regulations and guidelines. The CRA will also be the primary contact-point for investigational site staff.
Main responsibilities :
- Monitoring of clinical study sites as appropriate, including pre-study, initiation, monitoring and close-down meetings with clinical study investigators.
- Identification of clinical investigators.
- Review and preparation of study documents.
- Collation and copying of documents at the close of a project.
- Organisation and planning of study related meetings.
- Handling of telephone and other enquires from study site staff and clients during a study.
Experience needed :
The successful candidate must enjoy working independently and as part of a team. If you have a minimum of 1 years monitoring experience, you enjoy working in early stage of clinical research and wish to work in a lively consultancy environment with strong regulatory aspects of clinical development, them my client would like to hear from you.
My client is an expanding expert clinical and regulatory consultancy who can offer very good career progression and exposure.
If you are interested in hearing more please contact Natasha on 0207 5621791
The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the country where the job is based. Carlisle Staffing plc, trading as SRG is an Employment Business/Agency.
| Consultant: |
Natasha Grace |
