Clinical Trial Job at PSI CRO, Thailand | Life Sciences | Apply Now
If you are an early-career life scientist, a detail-oriented clinical research assistant, or a multilingual operational coordinator looking to advance your career within global trial management, this full-time role at PSI CRO is an exceptional opportunity. Located at our regional office in Bangkok, Thailand, this position places you at the critical intersection of investigator site relations, clinical trial documentation, and international study logistics. For organized professionals searching for a high-impact Clinical Trial Job, this position offers hands-on mastery over site feasibility tracking, clinical document compilation, and vendor payment administration. It serves as an elite operational milestone to build a long-term career within a premier global Contract Research Organization (CRO) and stands out as a top-tier choice for individuals looking to secure a high-growth Life Sciences Job in Southeast Asia.
- Job Position: Site Management Associate (Clinical Trial) (Verified job)
- Location: Bangkok, Bangkok City, Thailand (Hybrid)
About The Company
PSI CRO is a privately owned, full-service global Contract Research Organization (CRO) founded in 1995 that brings together 3,000 highly driven, dedicated individuals across the globe. Renowned in the pharmaceutical industry for its exceptional trial delivery timelines and high customer repeat-rate, PSI operates on the frontline of medical science, managing complex multi-center clinical trials for major biotech and pharmaceutical sponsors. The regional corporate office in Bangkok, Thailand, functions as a strategic clinical node for the Asia-Pacific territory. Joining the site management division at PSI means entering an organically grown, mature organization with highly refined standards and practices. Working in a fast-paced, international team structure, your day-to-day coordination ensures that clinical data regarding drug efficacy and safety are gathered seamlessly, helping bring breakthrough therapies to patients with serious medical conditions worldwide.
Key Responsibilities
The Site Management Associate functions as a vital central anchor for clinical research projects, working closely with investigative sites and study teams to streamline communications, maintain databases, and secure document compliance.
Your core site tracking, document control, and administrative duties include:
- Investigative Site Liaison: Serving as the primary in-house communication point for clinical investigative sites, managing day-to-day inquiries from physicians and site coordinators to advance this Clinical Trial Job.
- Clinical Database & Tracker Maintenance: Maintaining and meticulously updating internal clinical trial management databases, regulatory tracking systems, and enrollment logs.
- Dossier Documentation Governance: Compiling, procuring, processing, and filing large volumes of critical study documents, including investigator brochures, consent forms, and site greenlight binders.
- Vendor & Supply Access Coordination: Acting as the primary site contact point for third-party vendors, managing study supply shipments, and troubleshooting site access management issues for a premier Life Sciences Job.
- Query Resolution Alignment: Coordinating site-specific query resolution pipelines, tracking project training completions, and granting site teams access to vendor-related imaging or laboratory portals.
- Financial Payment Administration: Managing and ensuring the proper administration, verification, and processing of site-specific milestones and vendor payments.
- Project Meeting Coordination: Arranging complex project meetings, drafting detailed agendas, and capturing formal minutes of project team alignments.
- Office Logistics Triage: Receiving and routing incoming international calls, managing study mail vectors, and facilitating seamless cross-departmental communication.
Qualifications & Profile Requirements For Clinical Trial Job
PSI CRO seeks a flexible, proactive team player who demonstrates exceptional customer service skills and a positive attitude toward tackling complex project variables.
- Required Academic & Linguistic Criteria:
- Educational Foundation: A completed formal College or University Degree in the Life Sciences or a closely related natural science discipline.
- Linguistic Mastery: Full professional fluency in both written and spoken Thai and English is mandatory to communicate with local hospital sites and international project teams.
- Preferred Linguistic Asset: Additional professional proficiency in Japanese and/or Korean is a highly distinct advantage to support multi-national East Asian trial sites.
- Essential Knowledge & Experience:
- Industry Track Record: Prior administrative or operational support experience within a Clinical Research / CRO environment, preferably inside an international or multi-market corporate framework.
- Foundational understanding of the clinical trial lifecycle, clinical documentation parameters, and international Good Clinical Practice (GCP) guidelines.
- Strong organizational, planning, and multi-tasking skills, with a proven ability to prioritize tasks effectively in a fast-paced environment.
- High attention to detail, strong problem-solving abilities, and excellent interpersonal skills.
In short, the Site Management Associate position at PSI CRO is a definitive route to transitioning your life sciences degree or clinical assistant background into a highly marketable global asset. Securing an appointment here allows you to step away from repetitive data-entry mills and take direct operational charge of the investigator relations, database tracking networks, and document workflows that keep international clinical trials moving safely. If you reside in or can commute to Bangkok, meet the bilingual criteria, and possess a zero-error approach to document control, apply today to secure this premier choice in a Clinical Trial Job and launch an exceptional corporate Life Sciences Job.
