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パレクセルでの仕事

パレクセルは、臨床開発の上流から下流までのそれぞれの専門領域で、国内外の多くのお客様に高度なソリューションを提供するプロフェッショナル集団です。 パレクセルは、新しい薬や治療法を、それらを必要としている人々にいち早く届けることを目指し、日々の業務に取り組んでいます。

Future Opportunity: Clinical Trial Coordinator FSP – Istanbul

求人ID R0000035577 ロケーション イスタンブール, イスタンブール 仕事内容

Are you passionate about making a difference and ready to take the next step in your career? While we may not have a live vacancy at the moment, we’re always looking to connect with talented individuals who are interested in joining our team in the near future.

If you're excited about the possibility of working with us, we encourage you to submit your details today. Let’s start the conversation now, so we’re ready when the right opportunity comes along.

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.

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