Site Activation Lead — Start-Up & Study Delivery

Worldwide Clinical Trials; England; On-site; GBP 60,000 - 90,000; Full time

Job summary

Worldwide Clinical Trials is hiring a Site Activation Project Manager to lead start-up activities for trials. You will coordinate cross-functional teams, ensure critical path milestones are met, manage budgets, and drive site activation across regions in compliance with GCP and SOPs.

Requires a four-year life sciences degree or equivalent, plus 4+ years in CRO/pharma, strong leadership, and regulatory understanding. English communication and MS Office proficiency are essential.

Qualifications

• Four-year college curriculum with life science concentration or equivalent.
• Experience in clinical research or CRO/pharma environments.
• Proficiency in cross-cultural communication and regulatory awareness.

Responsibilities

• Own start-up and maintenance activities for study activation in assigned projects.
• Oversee functional teams to ensure on-time, on-budget progress.
• Prepare risk assessments and mitigation plans; coordinate budgets and CNFs.
• Contribute to SOPs and process improvements; support proposals and bids.

Skills

Leadership

Project management

Site activation

Regulatory knowledge

Cross-cultural communication

MS Office

Communication skills

Education

Four-year college curriculum in life sciences

Nursing or life science education (two-year)

Tools

MS Office (Word, Excel, PowerPoint)

Job description

Worldwide Clinical Trials is hiring a Site Activation Project Manager to lead start-up activities for trials. You will coordinate cross-functional teams, ensure critical path milestones are met, manage budgets, and drive site activation across regions in compliance with GCP and SOPs.

Requires a four-year life sciences degree or equivalent, plus 4+ years in CRO/pharma, strong leadership, and regulatory understanding. English communication and MS Office proficiency are essential.