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Parexel International
Parexel Senior Clinical Trial Associate Recruitment 2026: Apply Online
Senior Clinical Trial Associate (Project Specialist)
Experience Required
Minimum 2 years
Salary / Package
PLN 110,000 to 120,000 (Base Pay Range)
Work Mode
Remote (Home-based)
Openings
Multiple
Job Overview
- Provides logistical support to one or more global study management teams (SMT).
- Develops and maintains effective working relationships with SMT members, affiliate team members, and vendors.
- Assists Clinical Trial Manager (CTM) with effective communication between the SMT and Affiliates.
- Coordinates the management of all global supplies utilizing designated systems in collaboration with the CTM.
- Maintains and ensures the completeness of the Study-Level Trial Master File (TMF) in accordance with SOP requirements.
- Identifies and contributes to areas of best practice and process improvements.
- Ensures appropriate tracking and dissemination of Safety Reports during studies.
- Assists in the coordination of activities to ensure CRO and vendor delivery against the contracted scope of work.
Key Job Details
| Company Name | Parexel International |
| Job Role | Senior Clinical Trial Associate (Project Specialist) |
| Experience | Minimum 2 years |
| Salary Range | PLN 110,000 to 120,000 (Base Pay Range) |
| Job Type | Full-Time |
| Work Mode | Remote (Home-based) |
| Openings | Multiple |
| Job Location | Poland, Spain, Serbia, Romania (Remote) |
Key Responsibilities
- Coordinate global study supplies and manage meeting organizations.
- Maintain accurate tracking of health authority and IRB/IEC submissions in CTMS.
- Ensure completeness of Study-Level Trial Master Files (TMF) under CTM direction.
- Track and report study progress, maintaining communication channels across global teams.
- Comply with ICH-GCP guidelines, standard operating procedures, and training curricula.
Requirements & Qualifications
- Bachelor’s degree in life sciences, nursing, or equivalent.
- At least 2 years of experience as a project specialist in clinical research or health-related industries.
- Demonstrated experience working in global teams and familiarity with TMF.
- Strong knowledge of ICH/GCP guidelines.
- Proficiency in written and spoken English.
Required Skills
- Self-motivated, resourceful, and able to drive actions independently.
- Exceptional communication, collaboration, and teamwork abilities.
- High attention to detail and personal organization skills.
- Proficient computer literacy across multiple enterprise applications.
About Parexel International
Parexel is a leading global clinical research organization (CRO) dedicated to accelerating the delivery of life-changing treatments to patients worldwide through innovative clinical development, medical expertise, and patient-centric solutions.
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Frequently Asked Questions
Q: What is the primary role of a Senior Clinical Trial Associate at Parexel?
A: The role provides logistical support to global study management teams, maintains Trial Master Files (TMF), and assists with regulatory submissions and study tracking.
Q: Is this position remote?
A: Yes, the role is 100% home-based located in Poland, Spain, Serbia, or Romania.
Q: What educational qualifications are needed?
A: Candidates require a Bachelor’s degree in life sciences, nursing, or an equivalent health-related discipline.
Q: How much experience is required for this position?
A: A minimum of 2 years of experience working as a project specialist in clinical research or a health-related industry is required.
Q: What is the salary range for this role in Poland?
A: The base pay range for Poland is PLN 110,000 to 120,000, with eligibility for annual performance bonuses and comprehensive benefits.
Q: How can I apply for this job opening?
A: You can apply online by visiting the official Workday career portal through the direct apply link provided.
Disclaimer: This job post is prepared by collecting data from the official career page of Parexel International. We are not direct recruiters or representatives. Candidates should carefully review the requirements and policies on the company’s portal before initiating an application.