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Jobs at Parexel

We know just how important it is to put people first. It's with that human touch that we've played a part in nearly all of the top 50 treatments on the market. And every day, we're focused on working with industry leaders to bring life-changing healthcare to patients across the globe. Whether you join our Clinical, Consulting, Biotech, Functional Service Provider (FSP), or other teams, we're doing it With Heart ™.

Clinical Trial Coordinator (FSP)

Job ID 83053BR Poland, Remote

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.

Parexel FSP offers you the security of a long-term position and many opportunities for career progression.

We are currently recruiting talented and passionate people to join our FSP teams in Poland.

The Clinical Trial Coordinator position flexible office based in Warsaw gives you the opportunity to join a team with a wide range of experience and expertise.

Position Purpose:

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.

Primary Duties:

· Trial and site administration and support.

· Regulatory & Site Start-Up responsibilities.

· Collaborate with finance/budgeting representatives.

· Meeting Planning.

Skills and Education:

B.A./B.S. (Life Sciences preferred) or equivalent healthcare experience.

Minimum 1-2 years in Clinical Research or relevant healthcare experience (specific experience requirements may vary depending on the Country.

Fluent in Local Languages and business proficient in English (verbal and written).

Good understanding of Global, Country/Regional Clinical Research guidelines.

Effective time management, organizational and interpersonal skills, conflict management.

Effective communication with external customers (e.g., sites and investigators).

Able to work independently.

Join a global community where you can transform your career into a life-changing achievement.

Apply directly or contact us via email at


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