Clinical Studies Associate- 12 Month Contract

I am currently working with a top pharmaceutical company in Hertfordshire who is recruiting for a Clinical Studies Associate to join their global operations team on a 12-month contract. In this role you will be responsible for providing operational support to multiple cross-functional global Study Management Teams through all phases (phases 1b- IV) and stages of the study.

Some of your responsibilities will include:
*Develop and maintain effective working relationships with members of the Study Management Teams
*Assist the Global Studies Managers with effective communication and information sharing
*Contribute to the development, set up and maintenance of study specific tools
*Responsible for the input and management of data via the systems
*Point of contact for internal and external team members
*Review standard study related reports
*Identify any data or quality issues
*Responsible for communications between the study team and vendor for tasks and tracking information
*Ensure essential study information is tracked
*Responsible for the setup and coordination of all study team meetings
*Ensure adherence to GCP is followed across studies
*Assist with the induction of new starters within the group- coaching and mentoring

The company is looking for someone who has experience in:
*Clinical research experience in a CRO or pharma company
*Knowledge of ICH/GCP

The agency is looking to conduct interviews in the next 2 weeks so if you are interested in this role then please feel free to get in touch with Sabrina Deo at sdeo@pararecruit.com or 0121 616 3471/ 07824 452641

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