Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Clinical Trial Coordinator (S) / Project Specialist - FSP - Istanbul
Job ID R0000035838 , TurkeyAre you passionate about making a difference and ready to take the next step in your career?
Clinical Trial Coordinator (CTC) based in Istanbul.
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.
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.
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