Hybrid Clinical Trial Coordinator – Paris (Remote-friendly)

Parexel International; Paris; Hybrid; EUR 35,000 - 52,000; Full time

Benefits offered by this job

Medical Plan

Life Assurance

Pension

Job summary

Parexel International is seeking a Clinical Trial Coordinator to join our team in Paris in a hybrid capacity, 2–3 days per week. You will support studies from start-up through closure, coordinating with Clinical Research Managers, sites, and cross-functional teams to ensure smooth administration and regulatory compliance.

You will help manage budgets, documents, and trial master file activities, while developing expertise in clinical research operations within a fast-paced sponsor environment.

Qualifications

• B.A./B.S. degree, preferably in Life Sciences, or equivalent healthcare experience.
• 1–2 years of Clinical Research in a similar role.
• Good understanding of global and country/regional guidelines.
• Experience with clinical trial documentation and ETMF processes.
• Fluent in local language and business English.

Responsibilities

• Support Clinical Research Managers and study teams from start-up to close-out.
• Provide trial and site administration and operational support.
• Collaborate with budgeting and finance for study activities.
• Coordinate study meeting planning and logistics.
• Interact with sites, vendors, and internal stakeholders.
• Track and report negotiation activities related to study ops.
• Ensure compliance with financial procedures.
• Maintain study tracking tools and systems.
• Archive clinical trial documentation and records.
• Assist with eTMF reconciliation and document management.
• Support budgeting, agreements, and payments with stakeholders.

Skills

Org & Planning

Time Management

Interpersonal Skills

Conflict Management

Communication

Problem Solving

Independent Work

English Proficiency

Education

B.A./B.S. Life Sciences

Job description

Parexel International is seeking a Clinical Trial Coordinator to join our team in Paris in a hybrid capacity, 2–3 days per week. You will support studies from start-up through closure, coordinating with Clinical Research Managers, sites, and cross-functional teams to ensure smooth administration and regulatory compliance.

You will help manage budgets, documents, and trial master file activities, while developing expertise in clinical research operations within a fast-paced sponsor environment.