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Clinical Research Coordinator, Psych Med

2 weeks ago

Queenstown, Singapore National University Hospital Full time

**Overview of Role**

To conduct and oversee the implementation of clinical research and trials on cognitive impairment according to study protocol, SG-GCP, hospital policies, and applicable regulatory and ethics requirements and actively participate in management of junior staff.

**Roles and Responsibilities**
- Mentor and guide junior CRCs, providing guidance and on-the-job training on study protocols and best practices in clinical research.
- Develop and implement of training syllabi for new and existing CRCs to ensure compliance. Identify areas for continual improvements and develop plan for implementation to enhance and improve efficiency.
- Compliance with the SG-GCP and other applicable regulatory and ethical requirements and hospital policies.
- Monitor, track and provide resolution to all local study issues, keeping the Principal Investigator and study team members in the communication loop.
- Ensure proper collection, management and storage of biological samples and research data.
- Set up and maintain study investigator files, including records of consent taken and samples collection.
- Complete Case Report Forms (CRFs).
- Provide operational support and care coordination for memory clinic service.

**Requirements**:

- A degree or equivalent in qualifications in Science, Life Sciences, or Nursing. Minimum 3 years of clinical research experience.
- Fast learner who adapts quickly and takes initiative to solve problems.
- Responsible, able to work independently and collaborate as part of a team player.
- Demonstrates leadership, accountability, and ownership of tasks.
- Excellent project management skills and able to thrive under pressure in a fast-paced environment.
- Good written and communication skills.
- Proficient in other languages (Mandarin/Malay/Tamil) and/or Chinese dialects will be an added advantage due to the patient demographics of an elderly population.
- Meticulous attention to detail and documentation practices.
- Familiar with Good Clinical Practice (GCP) guidelines and the Human Biomedical Research Act (HBRA).
- Experience in phlebotomy is an advantage.