Clinical Research Associate II, Oncology
IQVIA
full-time
Posted on:
Location Type: Office
Location: Manchester • United Kingdom
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About the role
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements.
- Work with sites to adapt, drive, and track subject recruitment plan in line with project needs.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites.
- Evaluate the quality and integrity of study site practices and manage the progress of assigned studies.
Requirements
- At least 1 year of independent on-site monitoring experience of interventional studies in the UK.
- Good knowledge and skill in applying applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
- Good therapeutic and protocol knowledge as provided in company training.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Benefits
- Professional development opportunities
- Flexible working hours
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
site monitoringinterventional studiesclinical researchGood Clinical Practice (GCP)International Conference on Harmonization (ICH) guidelinesprotocol knowledge
Soft Skills
effective working relationshipscommunication