Clinical Research Coordinator

1 day ago

Hà Nội, Vietnam UNC Full time

**JOB ANNOUNCEMENT - CLINICAL RESEARCH COORDINATOR**

**Position**:Clinical Research Coordinator**

Full-time, based in Hanoi

**Report to**: Clinical Research Manager and Investigator of Record

**Position Summary**:
The Clinical Research Coordinator (CRC) will oversee and perform daily clinical trial activities to ensure the studies are conducted in compliance with protocols as well as local and international requirements. The CRC will work closely with participants, study teams, hospitals & healthcare organizations, the University of North Carolina at Chapel Hill experts, monitors, Institutional Review Boards (IRBs), sponsors, and other stakeholders to provide guidance and support for ongoing clinical studies.

**Duties & Responsibilities**:
**Study Coordination and Support**
- Coordinate study activities at the clinical research site, including participant scheduling, informed consent process, eligibility verification, treatment adherence monitoring, and safety monitoring
- Prepare documents and reports for Institutional Review Boards review and approval
- Develop case report forms and other tools for study data collection.
- Organize and deliver training for study staff on protocols, study procedures as per requirements of the study protocol, sponsors and applicable regulations
- Manage participant recruitment, retention, and community engagement activities
- Collaborate with healthcare facilities, research networks, and community partners to support study implementation
- Maintain meticulous records and documentation of all study activities, participant data, and regulatory compliance.
- Prepare progress reports, technical reports, and other study documentation

**Quality Assurance and Compliance**
- Develop Standard Operating Procedures (SOPs) and quality control processes
- Monitor daily study operations to ensure compliance with SOPs, Good Clinical Practice (GCP), and all applicable regulations
- Review consent forms, participant records, adverse event reports, and other study documents to verify data quality and integrity

**Study Operations**
- Develop plans for preparing research facilities, equipment, and staffing
- Participate in the development of study budget
- Oversee administrative and logístical tasks at the clinical research site
- Manage the work schedules and assignments of the clinical research staff
- Track and report on the completion of research milestones and metrics
- Coordinate the importation, procurement and maintenance of study equipment and supplies
- Perform other relevant duties as requested

**Required qualifications and skills**:

- Possess a MD degree
- Fluent in both spoken and written English
- Three years experience in clinical research preferred
- Excellent adaptability, interpersonal and organizational skills
- Attention to detail

**Salaries and Benefits**: A very competitive salary, benefits and full package of social, health & unemployment insurances as laws required

**How to**:
Job Details

Organisation:
UNC

Job location:
Hanoi

Application deadline:
2025-05-30

**Job Types**:
'Coordinator'

Sectors:
'National'

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