Clinical Trial Coordinator (Finance) - Paris, France (Hybrid) - FSP

Parexel; Paris; Hybride; EUR 35 000 - 50 000; Plein temps

Résumé du poste

A leading clinical research organization in Paris is seeking a Clinical Trial Coordinator to support clinical studies and various operational activities. You will collaborate with stakeholders, track negotiations, and manage trial documentation. The ideal candidate has a background in Life Sciences, with 1-2 years of experience in Clinical Research. This position offers a hybrid work environment and significant opportunities for career growth.

Prestations

Opportunities for long-term career development

Open and friendly work environment

Qualifications

• Minimum of 1-2 years in Clinical Research in a similar role.
• Fluent in local languages and proficient in English (verbal and written).
• Good understanding of global and regional clinical research guidelines.

Responsabilités

• Support the Clinical Research Manager and team throughout the study lifecycle.
• Collaborate with finance and budgeting teams.
• Interact with internal and external stakeholders to meet clinical study objectives.

Connaissances

Clinical Research

Time Management

Interpersonal Skills

Conflict Management

Formation

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

Description du poste

When our values align, there's no limit to what we can achieve.

Hybrid office-based in Paris, with the flexibility to go to the office a minimum of three days per week, based on business needs.

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

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

Join a single sponsor dedicated to a legendary pharmaceutical R&D powerhouse. A top 10 company behind a diverse array of medicines, therapies, and vaccines. Collaborate and learn alongside some of the industry's most experienced professionals.

Working as a Clinical Trials Coordinator at Parexel FSP offers an exciting platform to utilize your skills and develop your career in various directions. We aim to make a difference in millions of lives—and in your career!

Primary Responsibilities :

The Clinical Trial Coordinator (CTC) will support the Clinical Research Manager (CRM) and other team members throughout the study lifecycle, from start-up to closure.

Support trial and site administration, collaborate with finance and budgeting teams, and assist with meeting planning.

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

Track and report negotiations, ensure compliance with financial procedures, and maintain tracking tools and systems.

Assist with the electronic Trial Master File reconciliation, and handle budgeting, agreements, and payments.

Education and Experience :

B.A. / B.S. in Life Sciences or equivalent healthcare experience.

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

Fluent in local languages and proficient in English (verbal and written).

Good understanding of global and regional clinical research guidelines.

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

Ability to communicate effectively with external customers (e.g., sites and investigators).

Ability to work independently.

We value our people and your passion, which are key to our success. We provide an open, friendly work environment that empowers our staff and offers opportunities for long-term career development. You will have the chance to grow within your role, take on additional responsibilities, or explore other departments within Parexel.

Who are Parexel

Parexel supports clinical studies across a broad range of therapeutic areas and has longstanding partnerships with a diverse client base.

We have supported trials for most of today’s top 50 best-selling drugs, as well as niche developments critical to patient well-being.

You will be an influential member of our wider team.