Clinical Research Associate (CRA I or CRA II)
We are seeking experienced professionals to support our sponsor-dedicated team and conduct site monitoring visits across Scotland and Northern England.
Responsibilities
* Perform site monitoring visits, adhering to Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
* Work with sites to adapt, drive, and track subject recruitment plans to enhance predictability.
* Administer protocol and related study training to assigned sites and manage ongoing project expectations and issues.
* Evaluate the quality and integrity of study site practices, escalating quality issues as appropriate.
* Manage study progress by tracking regulatory submissions, approvals, recruitment, CRF completion, and data query generation and resolution.
Requirements
* 6 months + experience in independent on-site monitoring.
* Life science degree or equivalent industry experience.
* Flexibility to travel to sites across Scotland and Northern England.
Key Benefits
* Supportive leadership and collaborative teams.
* A variety of career opportunities to allow you to grow as we grow.
* Technology-enabled resources for efficient performance.
Estimated Salary:
£40,000 - £60,000 per annum, depending on experience.