Senior Clinical Trial Associate (Site Intelligence Specialist) - French Speaking - UK - FSP

Parexel; Uxbridge; On-site; GBP 40,000 - 55,000; Full time

Job summary

A leading company in the pharmaceutical industry is seeking a Senior Clinical Trial Associate (Site Intelligence Specialist) fluent in English and French. The role involves supporting Site Intelligence and Site Selection teams, executing feasibility plans, and maintaining databases. Ideal candidates are adaptable, detail-oriented, and have strong communication skills.

Qualifications

• At least 2 years of relevant experience.
• Experience working effectively with multiple functions.

Responsibilities

• Assist the Site Intelligence Lead to understand project goals.
• Review internal and external intelligence on performance metrics.
• Coordinate with teams to gather site feasibility data.

Skills

Fluent in English

Fluent in French

Strong presentation skills

Time management skills

Interpersonal skills

Education

Bachelor of Science

Tools

Microsoft Office Suite

Database applications

Job description

Senior Clinical Trial Associate (Site Intelligence Specialist) - French Speaking - UK - FSP

Parexel Uxbridge, England, United Kingdom

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Senior Clinical Trial Associate (Site Intelligence Specialist) - French Speaking - UK - FSP

Parexel Uxbridge, England, United Kingdom

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Parexel FSP offers an exciting opportunity for a Senior Clinical Trial Associate (Site Intelligence Specialist - SIS) to join our UK team. Candidates from other European locations such as France are also encouraged to apply.

The ideal candidate must be fluent in English (spoken and written) and have advanced or fluent proficiency in French. Knowledge of German, Hungarian, or Bulgarian is a plus.

Job Summary
The successful candidate will support Site Intelligence and Site Selection teams by performing tasks across multiple projects. They will assist in executing Site Feasibility plans and presenting data to colleagues.

Key Responsibilities

• Assist the Site Intelligence Lead to understand project goals, scope, and requirements, ensuring high-quality results.
• Review internal and external intelligence on performance and quality metrics; conduct literature research to identify investigators and build databases.
• Provide country-specific data (site contacts, recommendations) as requested, based on feasibility data collection and interpretation.
• Coordinate with internal and external teams to gather site feasibility data; help maintain the Investigator/Site Networks database.
• Update and verify data in client systems, spreadsheets, and documents.
• Promote continuous improvement to optimize processes.
• Maintain effective relationships across platform lines and research units to facilitate project delivery.

Skills and Experience

• Fluent in English and French; proficiency in German, Hungarian, or Bulgarian is advantageous.
• Experience working effectively with multiple functions in a professional environment.
• Proficiency in Microsoft Office Suite and database applications.
• Strong presentation, interpersonal, communication, and time management skills.
• Ability to multitask and work under tight deadlines with attention to detail.
• Flexible, adaptable, and capable of working independently or in a team within a matrix organization.
• Proven success in previous roles, demonstrating results-oriented performance.

Education

• Bachelor of Science or equivalent with at least 2 years of relevant experience.

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Additional Details

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job functions: Research, Analysis, Information Technology
• Industries: Pharmaceutical Manufacturing, Biotechnology Research, Healthcare