Experienced UK-based Regional CRA/clinical research associate required to augment existing CRA team, for a multinational biopharmaceutical company partner.
You will be part of an innovative and global biotechnology company, which prides itself on being one of the world's leading independent biotechnology companies. They focus on areas with unmet medical needs, aiming to reduce the social and economic burden of disease.
This is a rewarding position with a key global client, supported by a strong internal team, including a mentoring and training plan.
For this role, there is a requirement for only one internal interview with immediate feedback.
Responsibilities include:
1. Contributing to the selection of potential investigators.
2. Providing monitoring visit reports within required timelines.
3. Driving performance at sites, proactively identifying issues, and escalating as needed.
4. Performing source data verification according to SDV plan and resolving data queries.
5. Initiating, monitoring, and closing study sites in compliance with procedural documents, and sharing recruitment and site progress updates.
6. Training, supporting, and advising investigators and site staff on study matters.
Requirements include:
* Strong experience (approximately 2+ years) as a UK clinical research monitor (CRA), residing within the UK.
* Appropriate right-to-work in the UK.
* Driving license.
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