Looking for a clinical research coordinator who will be responsible for subject recruitment, data collection, and research administration at outpatient clinical sites.
This role requires close coordination with clinicians, researchers, and clinic staff to ensure the success of the study.
West Area
6 months
Monday to Friday: 8:00 AM – 4:30 PM
Saturday: 8:00 AM – 12:30 PM (5.5-day work week)
Key Responsibilities
1.
Subject Recruitment & Follow-Up
• Screen patients for eligibility and explain study procedures in simple terms.
• Obtain informed consent and administer questionnaires.
• Schedule appointments and manage follow-up with participants.
• Work closely with clinic teams and internal departments to meet recruitment targets and timelines.
2.
Research Documentation & Administration
• Manage data collection from participants and electronic health records.
• Maintain accurate and complete study records, including consent forms and biological sample logs.
• Input data into systems such as REDCap and hospital EHR platforms.
• Coordinate with investigators, clinicians, and labs to streamline workflows.
• Support submissions to Institutional Review Boards (IRB), including amendments and annual reports.
• Ensure compliance with HBRA, GCP guidelines, and audit requirements.
Requirements:
• Bachelor's Degree in Science, Public Health, Social Science, or related fields.
• At least 2 years of relevant experience preferred.
• Candidates with no experience are welcome to apply.
• Willing to travel between hospital and outpatient sites as required.
Interested applicants, Click APPLY with your resume
We regret to inform that only shortlisted candidates will be notified*
Lavia Tay (R
RecruitFirst Pte Ltd (E.A.13C6342)