Live opening · Posted 7 hours ago

Clinical Research Associate

SGB Medical Clinic & Clinical Research Center Inc. · Thailand (Remote)
Linkedin Yes
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At a glance

The key details from the original listing.

Posted 7 hours ago
CompanySGB Medical Clinic & Clinical Research Center Inc.
LocationThailand (Remote)
Work modeYes
SkillsClinical Research, GCP
SourceLinkedin
ListedPosted 7 hours ago

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About the role

Description supplied by the original job listing.

Job Title: Clinical Research Associate
Location: Thailand
Main Office: Singapore
Work Arrangement: Work From Home
Work Schedule: 5 Days per Week
Employment Type: Full-Time
Reports To: Clinical Operations Manager / Project Manager
Job Summary
The Clinical Research Associate (CRA) will be responsible for monitoring and supporting clinical trials conducted in Thailand. The CRA will work from home in Thailand and coordinate closely with the clinical research team based in the Singapore.
The position will ensure that clinical studies are conducted according to the study protocol, ICH-GCP, applicable Thai regulations, and company SOPs.
Key Responsibilities
Monitor assigned clinical trial sites in Thailand.
Conduct remote and on-site monitoring visits as required.
Coordinate with Principal Investigators, Study Coordinators, and site staff.
Ensure compliance with the study protocol, ICH-GCP, and applicable regulations.
Review study documents, patient records, and clinical trial data.
Identify and follow up on protocol deviations, data issues, and site concerns.
Monitor patient recruitment and study progress.
Review and maintain essential study documents.
Prepare monitoring reports and follow-up reports.
Support the management of clinical trial data and queries.
Communicate regularly with the clinical research team in Singapore.
Escalate important study issues and risks to the Clinical Operations Manager.
Support audits, inspections, and other clinical research activities when required.
Qualifications
Bachelor's degree in Nursing, Pharmacy, Medical Technology, Life Sciences, or a related field.
At least 2 years of experience in clinical research or clinical trials.
Previous CRA or clinical trial monitoring experience is preferred.
Knowledge of ICH-GCP and clinical trial processes.
Knowledge of Thai clinical research regulations is an advantage.
Good computer skills, particularly Microsoft Office.
Strong organizational and communication skills.
Ability to work independently in a work-from-home environment.
Willingness to travel within Thailand for site visits when required.
Language Requirements
Thai – Fluent
English – Good to Excellent, both written and spoken.
Work Arrangement
Work From Home while based in Thailand.
5-day work week, Monday to Friday.
Regular coordination with the main office and clinical research team in the Singapore.
Occasional travel within Thailand for clinical trial site visits and other study-related activities.
Preferred Skills
Good understanding of clinical trial monitoring.
Strong attention to detail.
Good communication and interpersonal skills.
Problem-solving and analytical skills.
Ability to manage multiple tasks and meet deadlines.
Ability to work effectively with international teams.

Work arrangement
Yes

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