Remote UK Study Start-Up Specialist – Clinical Trials

IQVIA LLC

Greater London

Remote

GBP 35,000 - 55,000

Full time

3 days ago

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Job summary

IQVIA is seeking a Country-level Site Activation professional to manage activation tasks for UK sites, working remotely with the SAM and project team. You will ensure regulatory readiness, maintain study documents, and monitor timelines in line with SOPs and ICH/GCP guidelines.

A background in life sciences and 3 years in clinical research are required. This home-based role requires strong knowledge of the UK clinical trial landscape and experience with regulatory submissions, ethics approvals,

Qualifications

Bachelor’s degree in life sciences or related field.
3 years clinical research experience.
In-depth knowledge of clinical systems, procedures, and corporate standards.
Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
Knowledge of local regulatory requirements, SOPs and company standards.
Understanding of regulated clinical trial environment and drug development process.

Responsibilities

Serve as Single Point of Contact (SPOC) in assigned studies for sites, SAM, PM team and other departments.
Perform start up and site activation activities according to regulations, SOPs and work instructions.
Distribute completed documents to sites and internal project team members.
Prepare site regulatory documents, reviewing for completeness and accuracy.
Maintain internal systems, databases and tracking tools with project information.
Review site performance metrics and provide feedback to management.
Assist in project planning and timeline establishment and monitoring.
Ensure monitoring measures are in place and implement contingency plans as needed.
Inform team of completion of regulatory and contractual documents for sites.