CRA2 - Multi-Sponsor Department

IQVIA LLC; Langley; On-site; GBP 35,000 - 55,000; Full time

Job summary

IQVIA is seeking a Clinical Trial Monitor to perform on-site visits, ensure GCP/ICH compliance, and manage site communications across multiple locations.

You will drive subject recruitment plans, administer protocol training, and track regulatory submissions to keep trials on track. Travel to sites is required as part of the role.

Qualifications

• Life science degree educated or equivalent industry experience.
• Independent on-site monitoring experience.
• Strong knowledge of GCP and ICH guidelines.
• Flexibility to travel to sites.

Responsibilities

• Perform site monitoring visits in line with GCP and ICH.
• Drive subject recruitment plans to enhance predictability.
• Administer protocol training and maintain site communication.
• Escalate quality issues and manage TMF/ISF documentation.
• Track regulatory submissions, recruitment, CRFs, and data queries.
• Collaborate with study team for project execution.
• Travel to sites as needed.
• Maintain and file site documentation.
• Ensure proper conduct of the protocol across sites.

Skills

Clinical monitoring

GCP expertise

ICH guidelines

On-site monitoring

Travel readiness

Education

Life science degree or equivalent

Job description

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
• Collaborate and liaise with study team members for project execution support as appropriate
• Experience of independent on-site monitoring
• You have successfully managed multiple clinical trial protocols across diverse investigative sites.
• In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Life science degree educated or equivalent industry experience
• Flexibility to travel to sites

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.