Remote UK Site Activation & Start-Up Specialist

IQVIA Argentina; Greater London; Remote; GBP 45,000 - 65,000; Full time

Job summary

IQVIA is seeking a Site Activation professional for a home-based role in the UK. You will serve as SPOC for investigative sites, manage site activation tasks, regulatory documentation, and adherence to GCP/ICH and SOPs, supporting SAMs and project teams. A life sciences degree and 3+ years in clinical research are required.

This role offers remote work within the UK and partnership with global sponsors. Responsibilities include coordinating regulatory submissions, maintaining project systems,

Qualifications

• Bachelor’s degree in life sciences or a related field.
• 3 years of clinical research experience.
• Knowledge of GCP/ICH and regulatory guidelines.
• Understanding of regulated clinical trial environment and drug development.

Responsibilities

• Serve as Single Point of Contact (SPOC) in assigned studies for sites, SAMs, PM team, and other departments.
• Ensure adherence to SOPs, WIs, quality of deliverables and project timelines.
• Perform start up and site activation activities according to regulations and SOPs.
• 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 and provide feedback on site performance metrics.
• Track project timelines and regulatory approvals.
• Provide local expertise to SAMs and project team during planning.
• Quality control of documents provided by sites.
• May have direct contact with sponsors on specific initiatives.

Skills

SPOC coordination

Regulatory knowledge

Project management

Quality control

Education

Bachelor’s degree in life sciences

Job description

IQVIA is seeking a Site Activation professional for a home-based role in the UK. You will serve as SPOC for investigative sites, manage site activation tasks, regulatory documentation, and adherence to GCP/ICH and SOPs, supporting SAMs and project teams. A life sciences degree and 3+ years in clinical research are required.

This role offers remote work within the UK and partnership with global sponsors. Responsibilities include coordinating regulatory submissions, maintaining project systems,