Clinical Research Associate

Clinical Research Associate, Permanent, UK - South East

My client, a leading global CRO who work across a broad range of therapeutic areas are looking for a CRA to join their team to work on trials at an international level.
Main Duties:
*To perform all clinical monitoring / site management activities for assigned projects in accordance with SOPs.
*To achieve and maintaining high site performance,
*managing clinical monitoring activities which include the ownership of investigator sites, the selection of investigator/sites, collating Regulatory Documentation, initiating and monitoring of sites,
*Performing site documentation verification, data collection and drug accountability in accordance with ICH GCP guidelines.
*There may also be the opportunity to also act as co-Clinical Lead or Clinical Lead.

Experience/Skills:

*Life Science degree
*Relevant monitoring experience within clinical research
*Excellent interpersonal, site management, relationship building, verbal and written communication skills including excellent presentation skills.
*Team player with outstanding negotiation and organizational skills.
*Client focused approach to work
*A flexible attitude with respect to work assignments
*Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail.
*Willingness to work with multiple supervisors/colleagues in a matrix environment, and to value the importance of teamwork.
*IT literate - Experience with Microsoft based applications
*Holds a driving licence.

Please send your CV to [Email hidden] to apply
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