Clinical Trial Coordinator (FSP) - Paris

Register your interest for a Clinical Trial Coordinator role with Parexel FSP

Hybrid/office-based in Paris.

Open to candidates with experience as Clinical Trial Assistant, Study Coordinator, Clinical Trial Coordinator, Project Support Associate, ICSM, CRA, or similar.

Play a pivotal role in some of the most significant clinical studies taking place today!

Single sponsor dedicated to a legendary pharmaceutical R&D powerhouse. A top 10 company and the name behind an incredible array of medicines, therapies, and vaccines. Collaborate, and learn, alongside some of the industry’s most experienced people.

Working as a Clinical Trials Coordinator at Parexel FSP provides an exciting platform for your skills, as well as the potential to develop into a variety of career paths. We make a difference in millions of lives. We’ll do the same for your career!

Primary Responsibilities:

The Clinical Trial Coordinator (CTC) will support the Clinical Research Manager (CRM) and other team members through the life cycle of the study from study start-up to study closure

Support the team members through the life cycle of a clinical trial from study start-up to study closure, performing the following duties:

• Trial and site administration and support.

• Collaborate with finance/budgeting representatives.

• Meeting Planning.

• Interact with internal and external stakeholders (study sites, vendors, etc.) in support of clinical study objectives.

• Tracking and reporting negotiations.

• Ensuring compliance with financial procedures.

• Maintenance of tracking tools and systems.

• Collate, distribute, and archive clinical documents.

• Assist with electronic Trial Master File reconciliation.

• Budgeting, Agreement, and Payments: Collaborate with finance/budgeting representatives.

• Meeting Planning

Education and Experience:

• B.A./B.S. (Life Sciences preferred) or equivalent healthcare experience.

• Minimum 1-2 years in Clinical Research in a similar role.

• Fluent in Local Languages and business proficient in English (verbal and written).

• Good understanding of Global, Country/Regional Clinical Research guidelines.

• Effective time management, organizational and interpersonal skills, conflict management.

• Effective communication with external customers (e.g., sites and investigators).

• Able to work independently.

About Parexel FSP

For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is the CRO trusted by life sciences companies to innovate keeping patients at the centre of everything we do, and where an inclusive global community helps you be your best, transforming any career into a life-changing achievement.

For an immediate telephone interview please contact the job poster.