Associate CRA: Clinical Monitoring Trainee

IQVIA; Livingston; On-site; GBP 25,000 - 35,000; Full time

Job summary

A leading global provider of clinical research services seeks a candidate for a clinical monitoring role in Livingston, Scotland. The role requires engagement in a structured training program, performing site monitoring visits, and ensuring adherence to clinical research protocols. Candidates should have a Bachelor's or Master's Degree in a relevant scientific discipline and good knowledge of clinical research regulatory requirements. The position offers a chance to make an impact in the healthcare industry.

Qualifications

• Bachelor's or Master's Degree in scientific discipline or health care preferred.
• Good knowledge of clinical research regulatory requirements (GCP and ICH).
• Experience within CRO, hospital or nursing setting preferred.
• Computer skills including proficiency in Microsoft Word, Excel and PowerPoint.
• Written and verbal communication skills including good command of English.
• Ability to establish and maintain effective working relationships.

Responsibilities

• Engage in a structured training program for clinical monitoring visits.
• Perform site monitoring visits under close supervision.
• Administer protocol and related study training to assigned sites.
• Evaluate the quality and integrity of study site practices.
• Manage the progress of assigned studies and regulatory submissions.
• Ensure documentation is available for filing in the TMF.

Job description

A leading global provider of clinical research services seeks a candidate for a clinical monitoring role in Livingston, Scotland. The role requires engagement in a structured training program, performing site monitoring visits, and ensuring adherence to clinical research protocols. Candidates should have a Bachelor's or Master's Degree in a relevant scientific discipline and good knowledge of clinical research regulatory requirements. The position offers a chance to make an impact in the healthcare industry.