Freelance Site Activation Specialist – Study Start-Up, Regulatory Submissions

🔥 0 minutes ago

🇬🇧 United Kingdom – Remote

⏳ Contract/Temporary

🟢 Junior

🟡 Mid-level

🚔 Compliance

🇬🇧 UK Skilled Worker Visa Sponsor

This company has sponsored UK Skilled Worker visas in the past.

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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IQVIA

WebsiteLinkedInAll Job Openings

10,000+ employees

💼 Consulting

🏭 Manufacturing

📣 Marketing

💰 $1G Post-IPO Debt on 2023-05

Consulting • Manufacturing • Marketing

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

📋 Description

• 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

🏖️ Benefits

• Freelance contract • Full-time equivalent (FTE 1.0) • Home-based work in the United Kingdom • Immediate start • Approximately 3–6 month engagement