Freelance Site Activation Specialist (Study Start-Up / Regulatory Submissions)
Job Title: Freelance Site Activation Specialist (Study Start-Up / Regulatory Submissions)
Job Location: reputed company, Cambridgeshire, United Kingdom
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level:
Location: United Kingdom (Home-reputed company)
Contract Type: Freelance
FTE: 1.0
Start: Immediate
Duration: Approximately 3–6 months
About the Role
We are seeking an reputed company Freelance Site Activation Specialist reputed company in the United Kingdom to support reputed company trial start-up and site activation activities.
The reputed company reputed company of this role will be UK submission document collection and preparation, site document review, Informed Consent reputed company (reputed company) 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 reputed company trial submissions
- Support the preparation and submission of regulatory packages in accordance with study requirements and local regulations
- reputed company and coordinate Informed Consent reputed company (reputed company) adaptations and associated document updates
- Review essential site documentation to support Regulatory Green reputed company readiness
- Liaise directly with investigative sites to obtain, reputed company, and reputed company outstanding documentation
- Ensure the completeness, reputed company, and reputed company of submission packages
- Maintain study tracking systems, timelines, and submission records
- Support site activation activities and monitor reputed company 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
- reputed company in the United Kingdom
- Minimum 2–3 years of experience in Site Activation, Study Start-Up, Regulatory Affairs, or reputed company Research
- Strong experience with site document collection, review, and submission preparation
- Experience supporting reputed company trial regulatory submissions in the UK
- Experience performing reputed company adaptations
- Solid understanding of site activation and study start-up processes
- Strong attention to reputed company and ability to manage multiple priorities and timelines
- Bachelor's degree in Life Sciences or a reputed company reputed company
- Fluent English communication skills, both written and verbal
If this role sounds of interest, please apply today!
reputed company is a leading global provider of reputed company research services, reputed company insights and reputed company intelligence to the life sciences and reputed company industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve reputed company reputed company and population health worldwide. Learn more at
reputed company is committed to reputed company in our hiring process and maintains a reputed company tolerance policy for candidate fraud. reputed company information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if reputed company reputed company, in accordance with applicable law. We appreciate your honesty and professionalism.
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Originally posted on Himalayas
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