⏳ Last Date to Apply: Not Mentioned
Parexel Clinical Research Associate II – Senior Recruitment 2026: Apply Online
Clinical Research Associate II – Senior
Job Overview
Overview of the Role
As a Clinical Research Associate (CRA) II or Senior CRA at Parexel, you will play a pivotal role in bringing life-saving treatments to patients globally. Your primary focus will be ensuring the safety, well-being, and rights of clinical trial participants while maintaining the highest standards of data integrity. This role requires a blend of scientific knowledge, meticulous attention to detail, and outstanding relationship-building skills as you act as the direct link between Parexel and clinical trial sites.
Key Areas of Impact
In this position, you will be responsible for the end-to-end management of clinical trial sites, from initial qualification through study close-out. You will collaborate closely with investigators and site staff to ensure strict adherence to study protocols, ICH-GCP guidelines, and local regulatory requirements. By performing both on-site and remote monitoring visits, you will proactively identify potential issues, implement corrective actions, and ensure that clinical trials are conducted efficiently and ethically.
Why Join Parexel?
Parexel offers a highly collaborative and supportive environment where your professional growth is prioritized. With a clear career progression pathway, you will have opportunities to transition into advanced technical roles, project leadership, or people management. Additionally, Parexel’s flexible work arrangements allow you to balance your professional responsibilities with your personal life, focusing on high-quality outputs rather than rigid schedules.
- Patient-Centric Culture: Put patients at the heart of everything you do, ensuring clinical trials are inclusive and innovative.
- Global Exposure: Work on diverse therapeutic areas and global projects alongside cross-functional teams.
- Advanced Technology: Utilize cutting-edge clinical trial management systems to streamline your monitoring duties.
Key Job Details
| Company Name | Parexel |
| Job Role | Clinical Research Associate II – Senior |
| Experience | Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology |
| Salary Range | Not Mentioned |
| Job Type | Full-Time |
| Work Mode | Flexible / Hybrid |
| Openings | Not Mentioned |
| Job Location | Kowloon, Hong Kong |
Key Responsibilities
- Act as Parexel’s direct contact with assigned clinical sites, assessing overall integrity of study implementation.
- Build and maintain strong professional relationships with investigators and site staff.
- Ensure clinical sites are compliant with project-specific training and protocol requirements.
- Identify, evaluate, and resolve data quality and data integrity issues at assigned sites.
- Perform on-site visits, including Qualification, Initiation, Routine Monitoring, and Close-out visits.
- Conduct remote monitoring contacts and generate detailed visit reports in a timely manner.
- Manage and track clinical trial supplies, including investigational product accountability and destruction.
- Maintain and update Clinical Trial Management Systems (CTMS) and ensure Trial Master File (TMF) completeness.
- Monitor compliance with ICH-GCP guidelines and applicable international and local regulations.
Requirements & Qualifications
- Proven site management experience or equivalent experience within clinical research.
- Solid understanding of clinical trial methodologies, terminology, and protocols.
- Willingness and ability to accommodate extensive travel requirements based on study phases.
- Valid driver’s license (where required locally).
- Ability to work independently with minimal oversight in a fast-paced environment.
Required Skills
- Strong problem-solving and analytical skills to address complex site issues.
- Excellent interpersonal, verbal, and written communication skills.
- Proficiency with clinical trial software (CTMS, EDC, EDMS) and MS Office products.
- Ability to prioritize multiple tasks and meet strict project timelines.
- Collaborative mindset to work effectively within a matrix and virtual team environment.
- High level of attention to detail and commitment to quality work.
About Parexel
Parexel is a leading global clinical research organization (CRO) dedicated to providing a comprehensive range of Phase I to IV clinical development services. With a mission to improve the lives of patients worldwide, Parexel combines scientific expertise, advanced technology, and a deeply compassionate culture to help biopharmaceutical companies bring innovative therapies to market faster and safer.
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