Associate CRA: Clinical Monitoring Trainee

IQVIA; Reading; On-site; GBP 30,000 - 40,000; Full time

Job summary

A leading global provider of clinical research services is seeking a Clinical Monitoring Associate in Reading, UK. The role involves engaging in a structured training program and conducting clinical monitoring visits under supervision to ensure compliance with study protocols and regulatory standards. Candidates should possess a Bachelor's or Master's degree in a scientific discipline or healthcare, along with good knowledge of GCP and ICH guidelines. Effective communication and relationship-building skills are essential for success in this role.

Qualifications

• Good knowledge of clinical research regulatory requirements (GCP & ICH).
• Experience within CRO, hospital, or nursing setting preferred.
• Right to work in the United Kingdom required.

Responsibilities

• Conduct clinical monitoring visits under supervision.
• Administer protocol-related training to assigned sites.
• Evaluate study site practices for adherence to protocols.
• Manage progress of assigned studies and documentation.
• Collaborate with study team members for project execution.

Skills

Good clinical practice (GCP)

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Written and verbal communication

Establishing working relationships

Education

Bachelor's or Master's Degree in scientific discipline or health care

Job description

A leading global provider of clinical research services is seeking a Clinical Monitoring Associate in Reading, UK. The role involves engaging in a structured training program and conducting clinical monitoring visits under supervision to ensure compliance with study protocols and regulatory standards. Candidates should possess a Bachelor's or Master's degree in a scientific discipline or healthcare, along with good knowledge of GCP and ICH guidelines. Effective communication and relationship-building skills are essential for success in this role.