At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with clinical guidelines.
- Company: Leading clinical research organisation in Manchester.
- Benefits: Competitive salary, travel opportunities, and professional development.
- Other info: Exciting role with opportunities for career advancement.
- Why this job: Join a dynamic team and contribute to groundbreaking clinical studies.
- Qualifications: 2+ years of monitoring experience and a relevant scientific degree.
The predicted salary is between 35000 - 45000 £ per year.
Clinical Research Associates in Manchester is seeking a skilled professional for site monitoring visits ensuring compliance with Good Clinical Practice and ICH guidelines. You will evaluate site practices, track study progress, and maintain documentation.
The ideal candidate will have at least 2 years of on-site monitoring experience in interventional studies and a relevant degree in a scientific discipline. A driving license is essential for travel to various sites.
CRA II: On-Site Monitoring & Study Coordination in Manchester employer: Clinical Research Associates
As a leading clinical research organisation in Manchester, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to excel in their roles. We offer competitive benefits, ongoing professional development opportunities, and a supportive environment that values work-life balance, making us an excellent employer for those passionate about advancing clinical research.
Contact Details:
Clinical Research Associates Recruitment Team
