Remote UK Clinical Study Start-Up Specialist

IQVIA; United States; Remote; USD 90,000 - 120,000; Full time

Job summary

IQVIA is seeking a Site Activation professional to manage country-level activities and coordinate with the SAM, PM team, and sites. This home-based role requires deep knowledge of the UK clinical trial landscape and submissions.

The candidate will perform site initiation, regulatory document review, and maintenance of internal systems, ensuring timelines and SOP adherence across studies.

Qualifications

• Bachelor’s degree in life sciences or related field is required.
• In-depth knowledge of GCP/ICH and regulatory guidelines.
• Experience in regulated clinical trial environments and drug development.

Responsibilities

• Serve as Single Point of Contact (SPOC) for sites and project teams.
• Perform site activation activities in line with SOPs and timelines.
• Prepare regulatory documents and maintain project records.
• Monitor compliance with regulatory, ethics, and ICF requirements.

Skills

GCP/ICH knowledge

Regulatory knowledge

Clinical research operations

Documentation accuracy

Education

Bachelor’s Degree in life sciences

Job description

IQVIA is seeking a Site Activation professional to manage country-level activities and coordinate with the SAM, PM team, and sites. This home-based role requires deep knowledge of the UK clinical trial landscape and submissions.

The candidate will perform site initiation, regulatory document review, and maintenance of internal systems, ensuring timelines and SOP adherence across studies.