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Senior Clinical Research Associate

IQVIA, Inc.

Reading

On-site

GBP 80,000 - 100,000

7 days ago

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An established industry player is looking for a Senior Clinical Research Associate to join a dedicated team supporting clinical sites across Ireland. This role offers a fantastic opportunity to work in a collaborative environment, where supportive leadership and career growth are prioritized. As a Senior CRA, you will be responsible for conducting site monitoring visits, ensuring compliance with regulatory standards, and managing study progress. This position is perfect for those who thrive on flexibility and enjoy working closely with clinical sites to enhance study outcomes. Join a forward-thinking company that values innovation and teamwork in the clinical research field.

Supportive leadership

Collaborative teams

Career growth opportunities

Technology-enabled resources

Minimum 12 months of independent on-site monitoring experience required.
In-depth knowledge of GCP and ICH guidelines is essential.

Perform site monitoring visits in accordance with GCP and ICH guidelines.
Manage the progress of assigned studies and ensure protocol adherence.

Good Clinical Practice (GCP)

International Conference on Harmonization (ICH)

Site Monitoring

Project Management

Life Science Degree

Equivalent Industry Experience

IQVIA are seeking a Senior Clinical Research Associate to join our sponsor-dedicated team and support sites across Ireland.

Excellent opportunity for CRAs local to Ireland or Northern Ireland who would value:

Supportive leadership and collaborative teams
A variety of career opportunities to allow you to grow as we grow
Technology-enabled resources that make doing your job more efficient

Responsibilities

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

Requirements

12 months minimum experience of independent on-site monitoring
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 across Ireland

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