英国/ROI站点SSU主管

Job Title: Site SSU Lead - UK/ROI (remote)
Job Location: Maidenhead
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level:

Fortrea is looking for an experienced Study Start-Up Lead to join our sponsor-dedicated team. If you enjoy leading study start-up activities, working with global teams, using data to drive smarter decisions, and helping clinical trials move forward efficiently, we'd love to hear from you.

What you'll be doing

As a Study Start-Up Lead, you'll play a key role in ensuring clinical studies are activated efficiently and ready to enroll participants on time. You'll work closely with cross-functional teams, provide guidance to site activation specialists, and help shape study start-up strategies across multiple countries.

Your responsibilities will include:

• Leading and supporting site activation teams across global clinical programs.

• Partnering with Clinical Operations teams to improve study start-up performance and timelines.

• Using data, forecasting tools, and industry insights to support planning and decision-making.

• Developing country-specific Informed Consent Forms (ICFs) based on local requirements and approved templates.

• Identifying opportunities to streamline processes and drive continuous improvement.

• Monitoring study progress, proactively addressing potential delays, and escalating issues when needed.

• Providing mentorship and guidance to study start-up team members.

• Collaborating with internal stakeholders to ensure sites achieve "Ready to Enroll" status as efficiently as possible.

• Acting as a key point of contact for study start-up challenges and helping teams find effective solutions.

What we're looking for

• Bachelor's degree in Life Sciences or a related field (or equivalent experience).

• 4+ years of experience in clinical operations, study start-up, project management, or trial optimization.

• At least 2 years of hands-on experience managing site activation and study start-up activities within a CRO or pharmaceutical environment.

• Experience creating country-level Informed Consent Forms (ICFs).

• Strong analytical skills with experience using data, forecasting tools, and performance metrics.

• Ability to interpret complex information and communicate it clearly to a variety of audiences.

• Solid understanding of the factors that contribute to successful study start-up and site activation.

• Previous experience working in a global clinical research environment is highly desirable.

• Strong communication, organizational, and stakeholder management skills.

Why join Fortrea?

• Be part of a global team committed to improving patient outcomes through clinical research.

• Work in a collaborative and supportive environment where your ideas are valued.

• Influence the success of international clinical trials and help bring new treatments to patients faster.

• Take ownership of meaningful projects and contribute to process improvements on a global scale.

• Enjoy opportunities for professional growth and career development within a leading CRO.

Ready to make an impact?

Join Fortrea and help shape the future of clinical research while working on studies that matter!

Learn more about our EEO & Accommodations request here.

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Originally posted on Himalayas