Clinical Trial Coordinator (R) - FSP (Istanbul)

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

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Inviting applications to join our EMEA Clinical Operations CTC team.

This role is hybrid office-based.

Open to candidates with experience as a Clinical Trial Associate, 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:

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

Tracking and reporting negotiations.

Regulatory and Study start-up tasks.

Maintenance of tracking tools and systems.

Collate, distribute, and, archive clinical documents.

Assist with electronic Trial Master File reconciliation.

Education and Experience:

• Trial and site administration and support experience.

· Regulatory & Site Start-Up experience,

· Meeting Planning.

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 center of everything we do, and where an inclusive global community helps you be your best, transforming any career into a life-changing achievement.