Location
Remote, based in Taiwan
Job Type
Contractor / Freelance
Part time, approximately 10 to 20 hours per week
Job Summary
ProPharma is seeking a Central Study Coordinator based in Taiwan to support a US based clinical study on a remote, part time contract basis. This position will be responsible for coordinating and supporting remote site activities for assigned projects, with a focus on site communication, document coordination, study support activities, and day to day operational follow through.
This role requires someone who can work independently, communicate effectively with sites and internal stakeholders, and operate confidently in a remote environment while maintaining accuracy, confidentiality, and compliance.
Key Responsibilities
- Serve as a point of contact for day to day site communications, document submissions, and study activity coordination
- Support pre screening, screening, and recruitment related activities as assigned
- Support subject re consenting, acquisition of medical records, and protocol related activities as directed by the Principal Investigator and study team
- Perform data entry, review and respond to system queries, and monitor clinical databases as assigned
- Establish and maintain timely communication with sites and internal stakeholders
- Maintain study documentation in compliance with IRB, FDA, ICH GCP, and applicable local requirements
- Assist with study closeout and other study related activities as directed
- Work effectively in a remote setting while maintaining privacy, professionalism, and attention to detail
- Collaborate with a US based study team and provide cross time zone support when needed
Required Qualifications
- Minimum 2 years of study coordinator experience
- Prior experience supporting clinical research activities, site coordination, or related study operations
- Fluency in Mandarin Chinese is required
- Working proficiency in English is required, both written and verbal
- Strong written and verbal communication skills
- Ability to work independently in a remote environment
- Strong organizational skills and ability to manage multiple tasks effectively
- Working knowledge of ICH GCP and applicable clinical research regulations and guidelines
- Comfortable using web based research platforms and Microsoft based systems
- Professional, well spoken, and articulate
- Ability to work from a private and secure remote location
Preferred Qualifications
- Experience supporting remote or decentralized site activities
- Experience working with global or US based study teams
- Study team experience in a clinical research setting
