đď¸ Be the Eyes and Ears of Groundbreaking Clinical Research in Thailand
ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, and medical device organizations. Our mission is to accelerate the development of therapies that improve patient lives.
We are seeking a Clinical Research Associate II (CRA II) to be our frontline expert for clinical trial monitoring in Thailand. In this vital role, you will ensure the integrity, compliance, and safety of our studies through expert site management. With at least 60% travel across the region, you will be the crucial link between ICON, investigative sites, and the patients who make medical breakthroughs possible.
đŻ YOUR MISSION: GUARDIAN OF DATA INTEGRITY & PATIENT SAFETY
You will independently manage and monitor clinical trial sites, ensuring strict adherence to protocols, ICH-GCP, and regulatory standards. Your expertise will safeguard data quality, protect patient rights, and drive the successful execution of clinical studies from start-up to close-out.
đ KEY RESPONSIBILITIES
đĽ Site Management & Monitoring
- Conduct all types of monitoring visits:Â site qualification, initiation, routine monitoring, and close-out.
- Ensure protocol compliance, accurate source data verification (SDV), and proper informed consent processes.
- Proactively identify and resolve site issues, ensuring patient safety and data integrity are never compromised.
đ Data Quality & Documentation
- Perform thorough data review, resolve discrepancies, and manage query resolution to maintain the highest data quality.
- Contribute to the preparation, review, and maintenance of essential study documentation, including protocols, reports, and the Trial Master File (TMF).
đ¤ Collaboration & Leadership
- Build strong, collaborative relationships with principal investigators and site staff to ensure smooth study conduct.
- Serve as a reliable point of contact for sites and internal project teams, providing expert guidance and support.
đ¤ YOUR PROFILE
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ESSENTIAL REQUIREMENTS
- Bachelorâs degree in Life Sciences, Pharmacy, Nursing, or a related healthcare/scientific field.
- Minimum of 2 years of independent, on-site monitoring experience as a Clinical Research Associate.
- In-depth knowledge of ICH-GCP guidelines, local regulatory requirements, and clinical trial processes in Thailand.
- Proven ability to travel at least 60% (domestic and international) to monitor sites.
- Exceptional organizational, communication, and problem-solving skills.
- Fluency in both Thai and English.
đ PREFERRED QUALIFICATIONS
- Experience across multiple therapeutic areas.
- Strong skills in risk-based monitoring and centralized monitoring techniques.
- Ability to work autonomously, manage multiple priorities, and thrive in a fast-paced, global environment.
đź WHY JOIN ICON AS A CRA IN THAILAND?
- Critical Impact:Â Your work directly ensures the safety of patients and the validity of data that leads to new treatments.
- Career Progression: Clear pathway to Senior CRA and Clinical Team Lead roles within a global CRO leader.
- Autonomy & Trust:Â Manage your own sites and travel schedule with the support of an experienced local and international team.
- Professional Development: Receive industry-leading training and support for ICH-GCP certification and skill advancement.
- Competitive Package:Â Enjoy a comprehensive salary, travel allowances, health insurance, retirement benefits, and well-being programs.
âď¸ READY TO TAKE YOUR CRA CAREER ACROSS THAILAND AND BEYOND?
đ APPLY NOW FOR THE CLINICAL RESEARCH ASSOCIATE II POSITION IN BANGKOK.
ICON is an Equal Opportunity Employer committed to fostering a diverse and inclusive workplace. We encourage all qualified applicants to applyâif you are a dedicated CRA looking to grow with a global leader, we want to hear from you.
