Clinical Trial Coordinator - Hybrid - Warsaw - FSP
at Parexel
zdalnie, województwo śląskie, Poland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 05 Feb, 2025 | Not Specified | 06 Nov, 2024 | 1 year(s) or above | Conflict Management,English,Interpersonal Skills,Clinical Research,Email,Time Management | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
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.
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
Responsibilities:
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.
REQUIREMENT SUMMARY
Min:1.0Max:2.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
BSc
Proficient
1
zdalnie, Poland