Senior Manager, Clinical Trial Feasibility & Site Identification

Advanced Clinical; Bristol; On-site; GBP 70,000 - 90,000; Full time

Job summary

A leading clinical research organization is seeking a Senior Manager for Clinical Trial Feasibility & Site Identification to lead strategies and site intelligence activities. This role involves active collaboration with cross-functional teams, analyzing data sources for study planning, and overseeing feasibility vendors to ensure project success. Candidates should possess expertise in feasibility methodologies and strong analytical skills. The position is remote and part of a flexible working model.

Qualifications

• Ability to influence decisions through data-driven insights and strategic thinking.
• Experience using real-world data, EMR/claims datasets, registries, or digital tools.
• Proven success partnering with CROs and vendors in feasibility execution.

Responsibilities

• Lead feasibility and site identification activities for assigned clinical trials.
• Provide strategic input to protocol design, enrollment planning, and geographic footprint.
• Analyze diverse data sources to deliver actionable insights at indication, country, and site levels.

Skills

Expertise in feasibility methodologies

Operational analytics

Strong collaboration skills

Communication skills

Organizational skills

Tools

CTMS

Reporting systems

Feasibility platforms

Job description

Senior Manager, Clinical Trial Feasibility & Site Identification

Remote | FSP Model via Advanced Clinical

We are seeking an experienced Senior Manager, Clinical Trial Feasibility & Site Identification to lead feasibility strategy and site intelligence activities across a dynamic clinical development portfolio. In this role, you will apply data-driven insights to inform study design, country and site selection, enrollment projections, and operational planning. You'll serve as the feasibility expert on Clinical Trial Working Groups (CTWGs) and collaborate closely with cross-functional teams and external partners to ensure successful trial placement and execution.

What You’ll Do

• Lead feasibility and site identification activities for assigned clinical trials
• Provide strategic input to protocol design, enrollment planning, and geographic footprint
• Analyze diverse data sources to deliver actionable insights at indication, country, and site levels
• Oversee feasibility vendors and CRO partners to ensure timely, high‑quality outputs
• Report feasibility progress, KPIs, and risk mitigation to study leadership
• Drive innovation by evaluating new tools, data sources, and operational models
• Support audit readiness through robust documentation and process adherence

What You Bring

• Expertise in feasibility methodologies, operational analytics, and site intelligence
• Ability to influence decisions through data-driven insights and strategic thinking
• Experience using real‑world data, EMR / claims datasets, registries, or digital tools (AI / ML, geomapping)
• Proven success partnering with CROs and vendors in feasibility execution
• Strong collaboration, communication, and organizational skills
• Proficiency with CTMS, reporting systems, and feasibility platforms