Skip Navigation

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 Regulatory - Hybrid - Warsaw - Poland - FSP

Job ID R0000022268 , Remote

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 marta.kuniewicz@parexel.com


#LI-REMOTE

Join our Talent Community

Welcome to the Parexel Talent Community! Sign up below and we’ll reach out with job alerts when positions that match your career interests become available. We’ll also share periodic updates about the latest company news and events.

Recently Viewed Jobs

You have not recently viewed any jobs

View all jobs

RECRUITMENT FRAUD ALERT

It has been brought to our attention that there has been fraudulent activity by scammers attempting to represent themselves as Parexel employees or recruiters. These individuals are attempting to reach potential job seekers through online chat interviews and sending false offer letters, representing Parexel without our consent. If you’re concerned that you’ve been contacted by an unauthorized Parexel recruiter or employee, please notify Jobs@Parexel.com. You may also report suspicious fraudulent activity to your local law enforcement agency or the FBI. Thank you.

@* *@