Clinical Trial Coordinator – FSP

Parexel

. Support Clinical Research Managers and study team members throughout the clinical trial lifecycle from study start-up to study closure .

Posted 10/8/2026full-timeParis • FranceJuniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical trial support, including trial administration, documentation management, and compliance with research guidelines. Proficient in collaborating with stakeholders and managing study-related financial activities.

Highest-signal resume keywords

Clinical Research ExperienceTrial Master File ProcessesStudy Documentation ManagementFinancial ComplianceStakeholder Communication

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical Trial AdministrationStudy Tracking ToolsBudgeting ProcessesRegulatory ComplianceDocumentation Archiving

Soft Skills

Organizational SkillsTime ManagementInterpersonal SkillsProblem-Solving SkillsConflict Management

Tools & Technologies

Electronic Trial Master FileTracking Systems

Industry Keywords

Life SciencesHealthcareClinical Research GuidelinesRegulated Environment

About the role

Key responsibilities & impact

Support Clinical Research Managers and study team members throughout the clinical trial lifecycle from study start-up to study closure
Provide trial and site administration and operational support
Collaborate with finance and budgeting representatives to support study-related financial activities
Coordinate and support study meeting planning activities
Interact with internal and external stakeholders, including study sites and vendors, in support of clinical study objectives
Track and report negotiation activities related to study operations
Ensure compliance with applicable financial procedures
Maintain study tracking tools and systems
Collate, distribute, and archive clinical trial documentation
Assist with electronic Trial Master File reconciliation activities
Support budgeting, agreement, and payment processes in collaboration with relevant stakeholders

Requirements

What you’ll need

B.A./B.S. degree, preferably in Life Sciences, or equivalent healthcare experience
Minimum 1 to 2 years of experience in Clinical Research in a similar role
Experience working in clinical research, healthcare, or a regulated environment
Good understanding of global and country/regional clinical research guidelines
Experience working with clinical trial documentation, tracking tools, and electronic Trial Master File processes
Fluent in local language and business proficient in English, both written and verbal
Strong organizational, time management, interpersonal, conflict management, communication, and problem-solving skills
Ability to collaborate across teams and communicate effectively with internal stakeholders and external customers, including sites and investigators
Patient-focused mindset and strong attention to detail
Ability to work independently
Comfort working with clinical trial documentation, tracking systems, and study support processes

Benefits

Comp & perks

Medical Plan
Life Assurance
Pension
Comprehensive benefits package for eligible employees
Flexibility
Growth opportunities