Clinical Trial Coordinator Job at Parexel | Apply Now
A Clinical Trial Coordinator Job at Parexel in Paris, France, offers aspiring coordinators a hybrid opportunity to support clinical research studies while collaborating with experienced professionals in the life sciences industry. Candidates with relevant experience are encouraged to apply.
- Job Title: Clinical Trial Coordinator
- Location: Paris, France – Remote
About Parexel
Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With over 22,000 employees worldwide, Parexel partners with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere. The organization emphasizes agility, bold thinking, and a commitment to addressing patient needs while accelerating the delivery of new therapies.
Clinical Trial Coordinator Job Description
As a part of the global Project Leadership group at Parexel, this clinical trial coordinator role is responsible for leading cross-functional teams to deliver high-quality and patient-focused clinical trials. This role involves collaborating with clients and internal stakeholders to identify project requirements, develop project plans, and manage project timelines and budgets. Strong leadership and communication skills are essential, along with a passion for improving patients’ lives.
Eligibility Criteria
- B.S. degree, preferably in Life Sciences, or equivalent healthcare experience.
- Minimum 1 to 2 years of experience in Clinical Research in a similar role.
- Good understanding of global and country/regional clinical research guidelines.
- Experience working with clinical trial documentation, tracking tools, and electronic Trial Master File processes.
- Strong communication, organizational, and problem-solving skills.
- Fluent in local language and business proficient in English, both written and verbal.
- Ability to work independently.
Key Responsibilities
- Support Clinical Research Managers and study team members throughout the clinical trial lifecycle from study start-up to study closure.
- Provide trial and site administration and operational support.
- Collaborate with finance and budgeting representatives to support study-related financial activities.
- Coordinate and support study meeting planning activities.
- Interact with internal and external stakeholders, including study sites and vendors, in support of clinical study objectives.
- Track and report negotiation activities related to study operations.
- Ensure compliance with applicable financial procedures.
- Maintain study tracking tools and systems.
- Collate, distribute, and archive clinical trial documentation.
- Assist with electronic Trial Master File reconciliation activities.
- Support budgeting, agreement, and payment processes in collaboration with relevant stakeholders.
Why Join Parexel
Parexel offers a supportive work environment that empowers employees to lead their studies effectively. The organization values flexibility, growth, and the contributions of its team members in shaping the future of clinical research. Employees are encouraged to take on new challenges and pursue their interests within a diverse set of clients and therapeutic areas.
Qualified candidates are encouraged to apply for this Clinical Trial Coordinator Job at Parexel before the deadline. This role is an excellent chance to contribute to meaningful clinical research and support the delivery of innovative therapies to patients.
