Senior Clinical Research Associate: Drive Site Excellence

IQVIA; Reading; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading clinical research company in the UK is looking for experienced Clinical Research Associates. Responsibilities include performing site monitoring visits, managing clinical trial protocols, and ensuring adherence to regulatory guidelines. Candidates should have at least 6 months of independent on-site monitoring experience and a life science degree or equivalent. Flexibility to travel to various sites is required. Join us to drive healthcare forward and make a significant impact in patient outcomes and population health.

Qualifications

• Minimum 6 months of independent on-site monitoring experience.
• Ability to manage multiple clinical trial protocols.
• In-depth knowledge of Good Clinical Practice (GCP) and ICH guidelines.

Responsibilities

• Perform site monitoring visits per regulatory requirements.
• Work with sites to enhance subject recruitment.
• Administer protocol training to assigned sites.
• Evaluate quality and integrity of site practices.
• Track studies' progress and manage regulatory submissions.
• Maintain accurate site management documentation.
• Collaborate with study team members.

Skills

Independent on-site monitoring

Clinical trial protocol management

Knowledge of GCP and ICH guidelines

Flexibility to travel

Education

Life science degree or equivalent experience

Job description

A leading clinical research company in the UK is looking for experienced Clinical Research Associates. Responsibilities include performing site monitoring visits, managing clinical trial protocols, and ensuring adherence to regulatory guidelines. Candidates should have at least 6 months of independent on-site monitoring experience and a life science degree or equivalent. Flexibility to travel to various sites is required. Join us to drive healthcare forward and make a significant impact in patient outcomes and population health.