Hybrid Clinical Trial Coordinator in Paris — Study Operations

Parexel; France; Ibrido; EUR 38.000 - 52.000; Tempo pieno

Vantaggi offerti da questo lavoro

Medical plan

Life assurance

Pension

Descrizione del lavoro

Parexel is seeking a Clinical Trial Coordinator to join our Paris team in a hybrid capacity (2–3 days/week in Paris). You will support study start-up through closeout, working with Clinical Research Managers and cross-functional partners to ensure timely administration, regulatory compliance, and document control.

Ideal candidates have 1–2 years in clinical research, strong organizational and communication skills, fluency in local language and professional English, and the ability to work

Competenze

• Minimum 1 to 2 years of experience in Clinical Research in a similar role.
• Familiar with clinical trial documentation and tracking tools.
• Knowledge of global and country/regional clinical research guidelines.
• Fluent in local language and business English.
• Ability to work independently.
• Strong communication and problem-solving skills.

Mansioni

• Support clinical trial lifecycle from start-up to closure.
• Provide trial and site administration and operational support.
• Collaborate with finance and budgeting for study activities.
• Coordinate study meeting planning.
• Interact with sites and vendors to meet objectives.
• Track and report negotiation activities related to study operations.
• Ensure compliance with financial procedures.
• Maintain study tracking tools and systems.
• Assist with TMF reconciliation and payment processes.

Conoscenze

Organizational skills

Time management

Interpersonal skills

Conflict management

Clinical research experience

Communication skills

Formazione

B.A./B.S. in Life Sciences

Descrizione del lavoro

Parexel is seeking a Clinical Trial Coordinator to join our Paris team in a hybrid capacity (2–3 days/week in Paris). You will support study start-up through closeout, working with Clinical Research Managers and cross-functional partners to ensure timely administration, regulatory compliance, and document control.

Ideal candidates have 1–2 years in clinical research, strong organizational and communication skills, fluency in local language and professional English, and the ability to work