⏳ Last Date to Apply: Not Mentioned
Parexel Clinical Research Associate II Recruitment 2026: Apply Online
Clinical Research Associate II
Job Overview
As a Clinical Research Associate II (CRA II) at Parexel, you will play an integral role in bringing life-saving treatments to patients faster. Your primary focus will be ensuring the safety, well-being, and rights of clinical trial participants while maintaining the highest standards of data integrity. In this role, you will act as the direct link between Parexel and assigned clinical investigator sites, ensuring that trials are conducted in strict compliance with study protocols, ICH-GCP guidelines, and applicable local regulations.
This is a dynamic, self-driven position that requires a high degree of accountability, organization, and relationship-building. You will travel to investigator sites to perform monitoring duties, conduct qualification and initiation visits, and manage site close-outs. Parexel offers a highly collaborative, supportive, and inclusive environment with diverse therapeutic area exposure, advanced technological tools, and structured career development pathways to help you grow professionally.
- Serve as the primary point of contact for assigned clinical trial sites.
- Ensure overall integrity of study implementation and adherence to protocols.
- Perform on-site and remote monitoring visits, generating detailed reports.
- Evaluate site recruitment plans and collaborate on improvement strategies.
- Manage clinical trial management systems (CTMS) and maintain the Trial Master File (TMF).
- Assess and manage investigational product supply and accountability.
Key Job Details
| Company Name | Parexel |
| Job Role | Clinical Research Associate II |
| Experience | Prior site management or equivalent clinical research monitoring experience. |
| Salary Range | Competitive Industry Standard |
| Job Type | Full-Time |
| Work Mode | Flexible (Hybrid/Home-based) |
| Openings | Multiple |
| Job Location | Taipei, Taiwan |
Key Responsibilities
- Act as Parexel’s direct contact with assigned clinical sites, assessing and ensuring overall integrity of study implementation.
- Build and maintain strong professional relationships with investigators and site staff.
- Facilitate site access to relevant study systems and ensure compliance with project-specific training requirements.
- Identify, evaluate, and resolve data quality and data integrity issues, implementing appropriate corrective actions.
- Conduct on-site visits, including Qualification, Initiation, Routine Monitoring, and Close-out visits.
- Perform remote monitoring contacts and generate comprehensive visit reports in a timely manner.
- Manage and reconcile investigational product/test article supply, accountability, and return/destruction status.
- Ensure assigned sites are continuously audit and inspection ready.
- Monitor and maintain strict compliance with ICH-GCP guidelines and local regulatory requirements.
Requirements & Qualifications
- Educated to degree level in biological science, pharmacy, nursing, or another health-related discipline.
- Proven site management experience or equivalent clinical research monitoring experience.
- Strong working knowledge of clinical trial methodology, terminology, and GCP guidelines.
- Ability to accommodate extensive travel requirements based on study phases and site allocations.
- Possession of a valid driver’s license (where required for site travel).
- Ability to work independently with minimal oversight in a self-driven capacity.
Required Skills
- Sound analytical and problem-solving skills to address complex site issues.
- Excellent interpersonal, verbal, and written communication skills.
- Strong computer literacy, including experience with CTMS, EDC, and MS Office products.
- Ability to prioritize multiple tasks and meet strict project timelines.
- Client-focused approach with the ability to interact professionally within sponsor organizations.
- Willingness to work effectively in a matrix and virtual team environment.
- High attention to detail and a strong sense of urgency in preserving patient safety.
About Parexel
Parexel is one of the world’s largest clinical research organizations (CROs), providing a comprehensive range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. With a compassionate, results-driven culture, Parexel puts patients at the heart of everything they do, fostering collaboration, inclusion, and continuous professional growth for its global workforce.
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