At a Glance
- Tasks: Support clinical trial start-up and site activation activities from home.
- Company: Join a leading organisation in clinical research with a focus on innovation.
- Benefits: Flexible freelance role, competitive pay, and the chance to work remotely.
- Other info: Collaborative environment with opportunities for professional growth.
- Why this job: Make a real difference in healthcare by supporting vital clinical trials.
- Qualifications: 2-3 years in Site Activation or Clinical Research and a degree in Life Sciences.
The predicted salary is between 29700 - 36300 £ per year.
Location: United Kingdom (Home-Based)
Contract Type: Freelance
FTE: 1.0
Start: Immediate
Duration: Approximately 3-6 months
About the Role
We are seeking an experienced Freelance Site Activation Specialist based in the United Kingdom to support clinical trial start-up and site activation activities. The primary focus of this role will be UK submission document collection and preparation, site document review, Informed Consent Form (ICF) adaptations, and regulatory submission support. The successful candidate will work closely with investigative sites and internal study teams to ensure submission packages are complete, compliant, and delivered according to project timelines.
Key Responsibilities
- Collect, review, and prepare site and regulatory documentation required for UK clinical trial submissions
- Support the preparation and submission of regulatory packages in accordance with study requirements and local regulations
- Perform and coordinate Informed Consent Form (ICF) adaptations and associated document updates
- Review essential site documentation to support Regulatory Green Light readiness
- Liaise directly with investigative sites to obtain, track, and resolve outstanding documentation
- Ensure the completeness, accuracy, and quality of submission packages
- Maintain study tracking systems, timelines, and submission records
- Support site activation activities and monitor progress against project milestones
- Collaborate closely with Site Activation Managers, Regulatory Affairs, Project Management, and other cross-functional teams
- Ensure compliance with ICH-GCP, local UK regulations, and study-specific requirements
Requirements
- Based in the United Kingdom
- Minimum 2-3 years of experience in Site Activation, Study Start-Up, Regulatory Affairs, or Clinical Research
- Strong experience with site document collection, review, and submission preparation
- Experience supporting clinical trial regulatory submissions in the UK
- Experience performing ICF adaptations
- Solid understanding of site activation and study start-up processes
- Strong attention to detail and ability to manage multiple priorities and timelines
- Bachelor's degree in Life Sciences or a related field
- Fluent English communication skills, both written and verbal
Freelance Site Activation Specialist (Study Start-Up / Regulatory Submissions) – UK Remote in London employer: QPL IQVIA RDS Poland Sp. z o.o.
IQVIA is an exceptional employer that fosters a collaborative and innovative work culture, where your contributions directly impact global health outcomes. With a strong emphasis on employee growth, you will have access to mentorship opportunities and professional development resources, all while working in a dynamic environment that values diversity and creativity. Located in a vibrant area, our team enjoys a supportive atmosphere that encourages meaningful work and personal fulfilment.
Contact Details:
QPL IQVIA RDS Poland Sp. z o.o. Recruitment Team
