Clinical Research Coordinator West

Job ID : )

Responsibilities :

• Conduct subject recruitment, screening, scheduling, and data entry based on study eligibility criteria.
• Communicate study objectives clearly to participants using layman terms and obtain informed consent.
• Administer study questionnaires and manage follow-up with participants.
• Collaborate with clinicians, clinic staff, and internal departments to meet research study requirements.
• Perform data collection from electronic health records and maintain accurate study documentation.
• Manage study investigator files, including consent forms and biological sample records.
• Maintain databases such as Redcap and electronic health record systems with high accuracy.
• Ensure strict adherence to research protocols including compliance with HBRA guidelines.
• Coordinate clinical workflows across multiple departments for recruitment activities.
• Prepare documentation for audits and support IRB submissions, amendments, and annual reports.
• Uphold professional conduct and record-keeping standards in line with hospital policies and ethics regulations.

Requirements :

We regret that only shortlisted candidates will be notified. However, rest assured that all applications will be updated to our resume bank for future opportunities.

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EA Personnel Name :  Felicia Chiam Kar Min

EA Personnel Reg. No. :  R

EA Licence No. :  07C5771

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