Senior Clinical Research Associate - Conversion

Obtain and maintain essential documentation in compliance with ICH-GCP, AZ Procedural Documents and local regulations both in the office and at site.

Actively participate in local Study Delivery Team meetings.

Contribute to the selection of potential investigators.

Train, support and advise Investigators and site staff in study related matters.

Contribute to national Investigators meetings.

Initiate monitor and close study sites in compliance with AZ Procedural Documents. Share information on patient recruitment and study site progress within local Study Delivery Team.

Drive performance at the sites. Proactively identify study-related issues and escalates as appropriate.

Update IMPACT and other systems with data from centres as per required timelines.

Manage study supplies (ISF, CRF, etc), drug supplies and drug accountability at study sites.

Per...