Clinical Research Associate I / II - FSP
Primary Location: Hong Kong Additional Locations: Hong Kong, Remote Job ID R0000042989 Category Clinical Trials Date Posted 08/25/2026
Overview
As a Clinical Research Associate (CRA) at Parexel, you act as an integral part to get treatments to patients sooner. Our CRAs' priority is the safety and well-being of the patients. As you travel to investigator sites and perform your monitoring duties, we encourage you to be inquisitive, take accountability, build relationships, and act with integrity.
Join a team with a wide variety of experiences and knowledge, and work on global projects within a broad scope of therapeutic areas. We’re looking for people who want to grow personally and professionally and support their colleagues globally and cross-functionally.
Success Profile
Do you have these soft skills and interpersonal traits to succeed at Parexel?
- Communicator
- Detail-oriented
- Flexible
- Organized
- Problem-solver
- Self-starter
About This Role
FSP CRA opening (Global Pharmaceutical Company FSP Team) for CRA I or II level.
This role requires to go to Client's office 1-2 days a week.
Key Accountabilities:
Study Team Supporting
Drive study performance at the sites. Perform site monitoring and other onsite visit activities according to monitoring plan and in compliance with procedural documents. Provide the required monitoring visit reports within required timelines. Proactively identify study-related issues and escalates to Local Study Teams as appropriate.
Contribute to the selection of potential sites and investigators. Train, support and advise Investigators and site staff in study related matters.
Obtain and maintain essential documentation in compliance with ICH-GCP, Procedural Documents and local regulations. Manage study supplies, drug supplies and drug accountability at study sites.
Perform source data verification according to SDV plan. Ensure data query resolution. Work with data management to ensure quality of the study data.
Ensure accurate and timely reporting of Serious Adverse Events.
Share relevant information on patient recruitment and study site progress within local Study Team. Update VCV and other systems with data from centers as per required timelines.
Prepare for activities associated with audits and regulatory inspections in liaison with local Study Team Lead and QA.
Adherence to AstraZeneca’s Code of Conduct and company policies and procedures.
Compliance with Parexel standards
Comply with required training curriculum.
Complete timesheets accurately as required.
Submit expense reports as required.
Update CV as required.
Maintain a working knowledge of and comply with Parexel processes, ICHGCPs and other applicable requirements.
Skills:
Understanding of the clinical dataflow.
Good knowledge of the clinical study and drug development processes, GCP/ICH guidelines and relevant local regulations.
Good computer skills in Microsoft and other software.
Fluent in both oral and written English
Proficient written and verbal communication skills, collaboration and interpersonal skills.
Knowledge and Experience:
Minimum 2-year experience as CRA, performed all tasks for a CRA position
Read, write, and speak fluent English; fluent in host country language required.
Education:
Bachelor’s degree in biological science or healthcare-related field., or equivalent
Potential Career Path
Parexel offers various career paths and internal development programs for CRAs to advance to the next level. This could include enhancing your technical position, moving into management, or shifting to other areas of the business.
- APEX CRA
- CRA I
- CRA II
- Senior CRA
- Project ManagementSubject Matter ExpertPeople Management
Employee Insights
TEAM IMPRESSIONS
Why Clinical Research Associates work at Parexel
