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Clinical Trial Coordinator

Thermo Fisher Scientific (Thailand)
Thermo Fisher Scientific (Thailand) (Bangkok, Bangkok City, Thailand)
Bangkok, Thailand 🇹🇭
Thermo Fisher Scientific (Thailand)
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.

Detail posisi

Thermo Fisher Scientific Inc. is seeking an individual with exceptional work behaviors to join our team as a Clinical Trial Coordinator (CTC) in Bangkok. As a CTC, you have to assist the clinical research teams in ensuring the most effective and efficient conduct of clinical research studies by providing administration and project tracking support.

Kewajiban

• Set up, organize and maintain accurate clinical study documentation (e.g. Trial Master Files etc.) and ensure compliance with regulatory requirements, including preparation for internal/external audits, final reconciliation and archival.
• Ensure that documents are up-to-date, complete, and readily accessible to the clinical research team, including quality control audits of clinical study documentation.
• Assist Clinical Operation teams with trial progress tracking by updating the Clinical Trial Management Systems, assist in the tracking and distribution of safety reports.
• Provide general administrative support to the Clinical Operations team with ongoing conduct of studies and completion of all required tasks to meet departmental and project goals, including co-ordination of Investigator payments, if applicable.
• Ensure successful completion of operational activities for clinical research studies within established timelines and quality standards.
• Collaborate with cross-functional teams to ensure successful implementation of study plans.
• Assist the Clinical Operations teams.
• Other duties as assigned.

Kualifikasi

• Bachelor's degree in medical, para-medical or scientific fields or equivalent experience.
• Clinical research or a related field is preferable.
• Exceptional attention to detail and organizational skills.
• Ability to manage multiple tasks and prioritization.
• Demonstrate critical thinking skills, resilience, agility.
• Strong communication and interpersonal skills, good written and spoken English.
• Computer literacy: e.g. Microsoft Word, Excel, PowerPoint, Outlook.
• Willingness to travel for job related activities if required.