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

Parexel International; France; Hybride; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A leading contract research organization is seeking a Clinical Trials Coordinator to support the lifecycle of clinical trials. This hybrid role based in Paris requires experience in clinical research and fluency in local languages and English. Join a team that plays a pivotal role in major clinical studies and offers opportunities for career development in a collaborative environment.

Prestations

Open and friendly work environment

Opportunities for career development

Qualifications

• Minimum 1-2 years in Clinical Research in a similar role.
• Fluent in local languages and business proficient in English.
• Good understanding of Global and Country/Regional Clinical Research guidelines.

Responsabilités

• Support the team through the lifecycle of a clinical trial.
• Collaborate with finance/budgeting representatives.
• Interact with internal and external stakeholders.

Connaissances

Clinical Research

Effective communication

Time management

Organizational skills

Interpersonal skills

Formation

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

Description du poste

Hybrid office-based in Paris, with the flexibility to go to the office as aminimum of three days per week andbased on the business need.

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.

We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of Parexel.

Who are Parexel

Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.

We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.

You’ll be an influential member of the wider team.

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