Site Monitoring Specialist

5 days ago


Reading, Reading, United Kingdom IQVIA, Inc. Full time

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:

  1. Conduct site monitoring visits to ensure compliance with regulatory requirements.
  2. Collaborate with sites to develop and implement effective recruitment strategies.
  3. Provide protocol and study training to assigned sites and establish ongoing communication.
  4. Review and evaluate study site practices to ensure compliance with regulatory requirements.
  5. Manage study progress through tracking regulatory submissions, recruitment, and data query resolution.
  6. Document site management activities and monitoring visit findings.
  7. Liaise with study team members to support project execution.

Requirements:

  1. Proven experience in on-site monitoring in the UK.
  2. Life science degree or equivalent industry experience.
  3. 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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