London - Sr Global Feasbility Manager

Job Summary:

Feasibility & Site Selection:

• Lead feasibility assessments for clinical trials, evaluating potential study sites, patient populations, and regulatory landscapes.
• Conduct site capability analysis to determine the best locations for clinical trial execution.
• Collaborate with internal stakeholders, sponsors, and site investigators to optimize trial design and recruitment strategies.

Market & Competitive Analysis:

• Analyze global and regional clinical trial trends, patient availability, and investigator experience.
• Assess regulatory requirements in China and international markets to ensure compliance.
• Provide data-driven insights to enhance clinical development strategies.

Stakeholder & Sponsor Engagement:

• Act as a key liaison between sponsors, investigators, and internal project teams to ensure alignment on feasibility findings.
• Prepare and present feasibility reports, feasibility questionnaires (FQs), and site selection recommendations to sponsors.
• Work closely with business development teams to support proposal development and strategic planning.

Regulatory & Compliance Considerations:

• Ensure all feasibility assessments align with ICH-GCP guidelines, regional regulatory requirements (e.g., NMPA, FDA, EMA), and CRO best practices.
• Collaborate with regulatory affairs teams to navigate local submission processes and optimize trial timelines.

Qualifications & Requirements:

• Language Proficiency: Fluent in Chinese (Mandarin) and English (spoken and written).
• Experience:
• 5+ years of experience in clinical trial feasibility and site selection within a global CRO or pharmaceutical company.
• 10+ years of experience in the clinical research or pharmaceutical industry.
• Education: Bachelor's or Master's degree in Life Sciences, Pharmacy, Medicine, or a related field.
• Technical Skills:
• Strong understanding of clinical trial operations, feasibility methodologies, and site feasibility analysis.
• Proficiency in clinical trial databases (e.g., CTMS, Site Selection Platforms), regulatory frameworks, and trial startup processes.
• Analytical & Strategic Thinking: Ability to assess complex trial feasibility data and provide actionable recommendations.
• Communication & Stakeholder Management: Strong ability to collaborate with cross-functional teams, present data-driven insights, and engage with global stakeholders.
• Global Mindset: Experience working on multi-country clinical trials with a deep understanding of Chinese and international clinical trial landscapes.

Preferred Qualifications:

• Experience in early-phase clinical trials (Phase I-II) or late-stage (Phase III) feasibility analysis.
• Familiarity with AI-driven feasibility tools and predictive analytics in clinical trial site selection.
• Experience working with Chinese regulatory agencies (NMPA) and international health authorities (FDA, EMA, MHRA, etc.).

• Be part of a leading global CRO, supporting innovative clinical research projects worldwide.
• Competitive salary, benefits, and career development opportunities.
• Work with a diverse and dynamic team, shaping the future of clinical trial feasibility and site selection.

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