Clinical Trial Coordinator (R) - FSP (Istanbul)
Istanbul, Türkiye Job ID R0000029411 Category Project Leadership Date Posted 11/13/2024Overview
As a part of the global Project Leadership group at Parexel, you are responsible for leading cross-functional teams to deliver high-quality and patient-focused clinical trials and help bring life-changing treatments to market faster. You collaborate with clients and internal stakeholders to identify project requirements, develop project plans, and manage project timelines and budgets. The role requires strong leadership and communication skills, the ability to work under pressure, and a passion for improving patients' lives.
In return, Parexel offers a supportive work environment, and a high degree of empowerment and accountability to lead your studies. Within this role, you work with a diverse set of clients and therapeutic areas, and you are encouraged to take on new challenges and pursue your interests.
Success Profile
Do you have these soft skills and interpersonal traits to succeed at Parexel?
- Adaptable
- Communicator
- Collaborative
- Leadership
- Proactive
- Problem-solver
About This Role
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.
#LI-TA1
Potential Career Path
Parexel offers a growth path with diverse therapeutic areas and clients, so you can grow according to your interests.
- Associate Project Leader
- Project Leader
- Senior Project Leader
- Associate Project Director
- Project Director
- Director, Project Leadership
- Senior Director, Project Leadership
Employee Insights
We do everything for patients
