Site Monitoring Specialist
5 days ago
About the Role
We are looking for an experienced Clinical Research Associate to join our team at IQVIA, Inc.
The ideal candidate will have a strong background in clinical research and excellent communication skills.
Responsibilities:
- Conduct site monitoring visits to ensure compliance with regulatory requirements.
- Collaborate with sites to develop and implement effective recruitment strategies.
- Provide protocol and study training to assigned sites and establish ongoing communication.
- Review and evaluate study site practices to ensure compliance with regulatory requirements.
- Manage study progress through tracking regulatory submissions, recruitment, and data query resolution.
- Document site management activities and monitoring visit findings.
- Liaise with study team members to support project execution.
Requirements:
- Proven experience in on-site monitoring in the UK.
- Life science degree or equivalent industry experience.
- Ability to travel to sites as required.
Salary Information:
This role offers a competitive salary range of £45,000 - £65,000 per annum, based on experience.
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