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Parexel International
Parexel Senior Clinical Research Associate Recruitment 2026: Apply Online
Senior Clinical Research Associate
Experience Required
Experienced (Site Management / Clinical Research)
Salary / Package
Competitive
Work Mode
Hybrid / Field-based
Openings
1
Job Overview
As a Senior Clinical Research Associate (CRA) at Parexel, you act as an integral part in bringing innovative medical treatments to patients sooner. Our CRAs prioritize the safety and well-being of clinical trial participants while traveling to investigator sites and performing rigorous monitoring duties.
- Serve as Parexel’s direct point of contact for assigned clinical sites.
- Assess and ensure overall study protocol adherence and data integrity.
- Perform on-site qualification, initiation, routine monitoring, and close-out visits.
- Maintain compliance with ICH-GCP and international/local regulatory frameworks.
- Collaborate globally and cross-functionally to achieve project timelines and milestones.
Key Job Details
| Company Name | Parexel International |
| Job Role | Senior Clinical Research Associate |
| Experience | Experienced (Site Management / Clinical Research) |
| Salary Range | Competitive |
| Job Type | Full-time |
| Work Mode | Hybrid / Field-based |
| Openings | 1 |
| Job Location | Hong Kong |
Key Responsibilities
- Manage assigned clinical sites from initiation through close-out, ensuring adherence to study protocols.
- Build and maintain strong professional relationships with investigators and site staff.
- Evaluate staff assignments, identify potential data quality issues, and implement corrective actions.
- Review, collect, and approve site regulatory documentation and ensure Trial Master File (TMF) completeness.
- Monitor test article supply, accountability, destruction status, and site payment status.
- Participate in internal/external audits, regulatory inspections, and investigator meetings.
- Update Clinical Trial Management Systems (CTMS) accurately and in a timely manner.
Requirements & Qualifications
- Sound problem-solving skills with the ability to take initiative and work independently.
- Strong presentation, client-focused approach, and professional interpersonal skills.
- Proficiency in computer applications, including CTMS, EDMS, and MS Office products.
- Effective time management and readiness to accommodate extensive travel requirements.
- Fluency in written and spoken Cantonese and English.
Required Skills
- Clinical Trial Monitoring
- ICH-GCP Compliance
- Site Management
- Problem-Solving & Analytical Thinking
- Effective Communication & Presentation
- Data Integrity Assessment
About Parexel International
Parexel is a leading global clinical research organization (CRO) providing robust biopharmaceutical development services. Driven by a patient-centric mission and a culture of compassion and innovation, Parexel helps pharmaceutical and biotech clients accelerate the delivery of life-changing treatments to patients worldwide.
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Frequently Asked Questions
Q: What are the primary responsibilities of a Senior Clinical Research Associate at Parexel?
A: Responsibilities include managing clinical sites from initiation through close-out, ensuring protocol compliance, maintaining data integrity, building investigator relationships, and monitoring patient safety.
Q: What educational background is required for this role?
A: Candidates must hold a degree in biological science, pharmacy, a health-related discipline, or an equivalent nursing qualification.
Q: Is travel required for this position?
A: Yes, the role involves performing on-site visits to investigator sites, qualification and initiation visits, and managing site supply chains.
Q: What language proficiency is necessary?
A: Candidates must be fluent in both written and spoken Cantonese and English.
Q: How can I apply for this position?
A: You can apply directly online through the official Parexel Workday career link provided in the job posting.
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.