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Parexel International
Parexel Clinical Research Associate I/II/Senior Recruitment 2026: Apply Online for Various Vacancies
Clinical Research Associate I/II/Senior
Experience Required
Site Management experience or equivalent experience in clinical research
Salary / Package
Competitive Industry Standard
Work Mode
Hybrid / Flexible
Openings
Various
Job Overview
Parexel is seeking highly motivated and dedicated professionals to join our global clinical operations team as a Clinical Research Associate (CRA) I, II, or Senior CRA in Taipei, Taiwan. As an integral part of our mission, you will play a crucial role in getting life-changing treatments to patients faster and safer. Our CRAs are the frontline ambassadors of clinical trials, ensuring the highest standards of patient safety, data integrity, and protocol compliance across diverse therapeutic areas.
In this role, you will act as the primary point of contact for assigned clinical investigator sites. You will build strong, collaborative relationships with investigators and site staff, guiding them through the complexities of clinical trial protocols. Your day-to-day responsibilities will involve a dynamic mix of on-site monitoring, remote data review, and administrative management. You will perform qualification, initiation, routine monitoring, and close-out visits, applying your clinical research expertise to resolve site issues and ensure first-time quality.
Key aspects of the Clinical Research Associate role at Parexel include:
In this role, you will act as the primary point of contact for assigned clinical investigator sites. You will build strong, collaborative relationships with investigators and site staff, guiding them through the complexities of clinical trial protocols. Your day-to-day responsibilities will involve a dynamic mix of on-site monitoring, remote data review, and administrative management. You will perform qualification, initiation, routine monitoring, and close-out visits, applying your clinical research expertise to resolve site issues and ensure first-time quality.
Key aspects of the Clinical Research Associate role at Parexel include:
- Site Management & Relationship Building: Establishing trust and open communication with site staff to facilitate smooth trial execution and high recruitment compliance.
- Protocol & Regulatory Compliance: Ensuring all clinical activities strictly adhere to the study protocol, ICH-GCP guidelines, and local regulatory requirements in Taiwan.
- Data Integrity & Quality Assurance: Reviewing Case Report Forms (CRFs), source documents, and resolving data queries to maintain the highest standards of clinical data quality.
- Trial Documentation: Managing and maintaining the Trial Master File (TMF) and Investigator Site Files (ISF) to ensure they are audit and inspection-ready at all times.
- Investigational Product Accountability: Monitoring the supply, storage, and proper destruction or return of investigational drugs or medical devices.
Key Job Details
| Company Name | Parexel International |
| Job Role | Clinical Research Associate I/II/Senior |
| Experience | Site Management experience or equivalent experience in clinical research |
| Salary Range | Competitive Industry Standard |
| Job Category | Graduation Jobs, Private Jobs |
| Job Type | Full Time |
| Work Mode | Hybrid / Flexible |
| Openings | Various |
| Job Location | Taipei, Taiwan |
Key Responsibilities
- Act as PAREXEL’s direct contact with assigned sites, assess and ensure overall integrity of study implementation and adherence to study protocol.
- Build relationships with investigators and site staff.
- Facilitate and support site with access to relevant study systems and ensure compliance with training requirements.
- Perform on-site visits including Qualification, Initiation, Monitoring, and Close-out visits.
- Conduct remote visits/contacts as requested or needed and generate visit reports.
- Evaluate overall compliance and performance of sites and site staff.
- Manage test article/study supply including supply, accountability, and destruction/return status.
- Update Clinical Trial Management Systems (CTMS) and manage Trial Master File (TMF) documents.
- Monitor and maintain compliance with ICH-GCP and applicable international and local regulations.
Requirements & Qualifications
- Educated to degree level (biological science, pharmacy, or other health-related discipline preferred) or equivalent nursing qualification.
- Site Management experience or equivalent experience in clinical research.
- Strong understanding of clinical trials methodology and terminology.
- Ability to accommodate extensive travel time requirements.
- Holds a valid driver’s license where required.
Required Skills
- Sound problem-solving and analytical skills.
- Ability to take initiative and work independently.
- Advanced presentation and professional interaction skills.
- Client-focused approach to work with a flexible attitude.
- Strong computer skills including CTMS, EDMS, and MS-Office products.
- Strong interpersonal, verbal, and written communication skills.
- Effective time management and ability to work in a virtual team environment.
About Parexel International
Parexel is a leading global clinical research organization (CRO) focused on delivering treatments to patients sooner. With a compassionate and results-driven culture, Parexel prioritizes patient safety, clinical excellence, and professional growth for its employees.
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Frequently Asked Questions
Q: What is the educational qualification required for the CRA role at Parexel?
A: Candidates should be educated to degree level, preferably in biological science, pharmacy, nursing, or other health-related disciplines.
Q: Where is this Clinical Research Associate position located?
A: The position is based in Taipei, Taiwan, with flexible and hybrid work options available.
Q: Does this role require travel?
A: Yes, candidates must be able to accommodate extensive travel requirements according to the phases of the assigned clinical studies.
Q: What are the key systems used by CRAs at Parexel?
A: CRAs regularly use Clinical Trial Management Systems (CTMS), Electronic Data Capture (EDC), and Electronic Document Management Systems (EDMS).
Q: Is there a career progression path for CRAs at Parexel?
A: Yes, Parexel offers structured career development pathways from CRA I, CRA II, to Senior CRA, and further into Project Management or People Management.
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.