Clinical Trial Coordinator Regulatory - Hybrid - Warsaw - Poland - FSP
Poland, Remote Job ID R0000022268 Category Clinical TrialsAbout this Role
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
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