Senior Clinical Research Associate (CRA) – Bangkok, Thailand
Location: Bangkok, Thailand (Hybrid)
Employment Type: Full-Time
Job ID: R1520819
Experience Required: 3–6+ years in Clinical Research or CRA roles
Industry: Clinical Operations | Life Sciences | Pharmaceuticals
Job Overview
IQVIA Thailand is expanding its Clinical Operations team and is seeking an experienced Senior Clinical Research Associate (CRA) to ensure the successful execution, monitoring, and oversight of clinical trials. This role is ideal for professionals with a solid background in site management, clinical monitoring, and regulatory compliance, looking to advance their career in international clinical research.
The CRA will monitor clinical sites to ensure adherence to protocol requirements, Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, and sponsor expectations. The position involves both field-based monitoring and hybrid remote responsibilities, supporting trials across therapeutic areas.
Key Responsibilities
Site Management & Monitoring
Conduct site visits including selection, initiation, monitoring, and close-out in compliance with regulatory and sponsor requirements.
Train site staff on study protocols and establish effective communication channels to manage project expectations.
Evaluate site performance and ensure compliance with GCP, ICH guidelines, and protocol standards.
Support subject recruitment strategies at individual sites to optimize enrollment and retention.
Study Oversight & Documentation
Track study progress including regulatory submissions, approvals, CRF completion, and data query resolution.
Maintain Trial Master File (TMF) and Investigator Site File (ISF) in compliance with local regulations and GCP standards.
Generate detailed monitoring visit reports, follow-up letters, and other essential documentation for internal and sponsor review.
Collaboration & Communication
Collaborate closely with project teams, clinical operations staff, and site personnel to ensure smooth trial execution.
Provide guidance on site financial management per clinical trial agreements and local requirements, if applicable.
Required Qualifications & Experience
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related scientific/healthcare discipline.
Minimum 3–6 years of CRA experience, including hands-on site monitoring and clinical trial management.
Strong knowledge of clinical research regulations including GCP, ICH guidelines, and local regulatory requirements.
Proficiency in Microsoft Word, Excel, PowerPoint, and use of mobile devices for clinical monitoring.
Excellent verbal and written communication skills in English.
Strong organizational, problem-solving, and time management skills, with the ability to handle multiple sites and trials simultaneously.
Preferred Skills
Experience in site financial management and subject recruitment planning.
Prior exposure to hybrid monitoring models and remote trial management.
Familiarity with therapeutic areas or prior experience in multi-regional clinical trials.
Why Join IQVIA
Opportunity to work with global leaders in clinical research, life sciences, and healthcare intelligence.
Exposure to innovative clinical trials and international regulatory environments.
Professional development through mentorship, global collaborations, and advanced clinical operations projects.
Hybrid work model with flexibility and support for field visits across Thailand.
About IQVIA
IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence. We leverage technology and analytics to accelerate the development and commercialization of innovative therapies, improving patient outcomes and population health worldwide.
Apply now to join IQVIA Thailand and contribute to cutting-edge clinical research initiatives.
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