Skip to main content

This job has expired

Clinical Trial Coordinator (R) - FSP (Istanbul) Register your interest

Istanbul, Turkey
Start date
14 Jun 2024
Closing date
30 Jun 2024

Job Details

Inviting applications to join our EMEA Clinical Operations Talent Pipeline. Please provide some basic information and upload your resume. As soon as the role becomes available, we will promptly send you an invitation to apply officially .

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.

• 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.




When you join us, you’re joining a team that sees everything they do as an opportunity to transform the world for patients everywhere. When our employees bring their many perspectives together to tackle a new challenge, there’s no limit to what they can accomplish. Through it all, at the center of all we do, is a patient whose life could change – forever. And together, we’ll do it With Heart™.

How to describe Parexel’s culture in one word: 




Working With Heart™ - Christina's perspective:

Working With Heart™ - Christina's perspective:


Careers Blog | Our Culture | Diversity, Equity & Inclusion | Benefits | Our Hiring Process

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help lifesaving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory, and therapeutic expertise, our team of more than 21,000 global professionals works in partnership with biopharmaceutical leaders, emerging innovators, and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. 

Company info
+44 1895 238000
The Quays
101-105 Oxford Road

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert