Clinical Research Associate CRA
External job listingat Bryan Zulueta
Support clinical research and trials as a Clinical Research Associate CRA, conducting monitoring, compliance reviews, and site support.
Salary
Not provided
Location
Manila, Philippines
Employment type
Full time
Workplace
Not provided
Clinical Research Associate CRA
Manila, Philippines
Job description
About the role
Bryan Zulueta is looking for a qualified and experienced Clinical Research Associate (CRA) to support clinical research and clinical trials. The role involves working remotely with the Singapore-based Clinical Research & Operations Team and providing research and clinical trial site support.
Responsibilities
- Conduct remote and/or site monitoring visits, including quality, compliance, data integrity monitoring, and close-out visits.
- Ensure compliance with study protocols, ICH-GCP, and applicable regulations.
- Review source documents, essential documents, and clinical trial data upon request.
- Identify and resolve protocol deviations, data queries, and site issues.
- Monitor study progress, recruitment, enrollment, and site performance.
- Prepare monitoring reports and required documentation.
- Coordinate investigations, study coordinators, and research teams.
- Support other clinical research activities as assigned.
- Travel when required for on-site monitoring and other study-related activities.
Requirements
- Filipino citizen based in the Philippines.
- Bachelor’s degree in Nursing, Pharmacy, Life Sciences, Medicine, Medical Technology, or a related field.
- Minimum 2 years of experience in clinical research as a clinical CRA.
- Prior CRA and clinical trial monitoring experience is preferred.
- Experience conducting and/or remote monitoring visits.
- Good understanding of ICH-GCP and clinical trial regulations.
- Strong organizational, analytical, documentation, and communication skills.
- Proficiency in English and ability to work independently and effectively.
- Willingness to travel when required.
Benefits
- Full-time employment and a work-from-home arrangement.
- 5-day work week.
- Opportunity to work with an international clinical research team.
- Exposure to additional clinical research projects and stakeholders.
Key facts
- Full-time employment with a work-from-home arrangement.
- 5-day work week.
- Requires a bachelor’s degree in a related field and minimum 2 years of clinical research experience as a clinical CRA.
- Travel when required for on-site monitoring and other study-related activities.
Frequently asked questions
What does the role involve?
It supports clinical research and clinical trials, including monitoring visits, compliance reviews, documentation, and site support.
What qualifications are required?
The role requires a bachelor’s degree in a related field and minimum 2 years of experience in clinical research as a clinical CRA.
Is travel required?
Travel is required when needed for on-site monitoring and other study-related activities.