Description
Are you an innovative, assertive and analytical Clinical Research Associate looking for an exciting opportunity in a research and development driven company?The Clinical Research Associate will manager allocated study sites to ensure that timelines, recruitment and quality standards are met on all clinical trial projects.
Key Responsibilities:
-Maintain awareness of ICH GCP, SOP's and regulatory requirements and ensure adherence by site staff
-Take ownership of costumer queries or complaints and seek timely resolution
-Resolve any non-compliance and data quality issues(protocol violations, ICH GCP, SOP's) and feedback to clinical monitor -Manage 10-20 sites across a variety of projects and therapy areas
-Set own challenging targets, standards and objectives consistently delivering performance in excess of them
-act as a source of expertise on subjects/issues in clinical research
-Able to deputise for Local clinical Monitor as appropriate
-Proactive in coaching others and sharing best practise
Requirements:
-Graduate Life Science/Nursing or Nursing qualification(RGN or equivalent)
-Working knowledge of ICH GCP and clinical trial methodology
-Some knowledge of relevant industry standards and other legislation
-Experience in one or more of oncology, virology, respiratory or diabetes, Experience of Crohns disease would be an advantage -12 months monitor experience
This is a fantastic opportunity to gain a wealth of experience in a highly regarded and global pharmaceutical company. If you are interested in this role and have the relevant skills and experience please contact me Anna Mooney or apply below with an up to date CV.
To find out more about Real please visit www.realstaffing.com