Roles & Responsibilities
๐ Location : Queenstown
๐ Work Schedule :
Monday to Friday : 8 : 00 AM โ 4 : 30 PM
Saturday : 8 : 00 AM โ 12 : 30 PM (required)
๐ฐ Salary : Up to $3,400 / month
๐ Key Responsibilities :
๐งช Subject Recruitment & Follow-Up :
Recruit and schedule study participants; screen for study eligibility.
Explain study objectives to potential participants in layman terms and obtain informed consent.
Administer study questionnaires and conduct follow-up with study participants.
Collaborate with clinicians, research teams, and clinic staff to ensure study needs are met.
๐ Research Documentation & Administrative Duties :
Carry out study procedures including patient recruitment, data collection, and data entry.
Extract data from electronic health records (EHR) and maintain study databases (e.g., Redcap).
Set up and manage investigator files and consent records.
Coordinate IRB submissions, amendments, and annual reports.
Ensure full compliance with study protocols and regulations (e.g., HBRA).
Support audits and maintain proper research documentation.
Work closely with investigators, clinicians, and labs to set up workflows for recruitment across departments.
โ Requirements :
Min. Degree in any related field
Prior experience in clinical research or healthcare setting is a plus.
Strong interpersonal and communication skills.
Comfortable working with patients and multidisciplinary teams.
Highly organised, detail-oriented, and able to meet tight deadlines.
Familiarity with research systems (e.g., Redcap, EHR) and ethical guidelines (HBRA) is an advantage.
If interested, please email me at Kellyn@recruitexpress.com.sg or telegram @kellynlytan
Kellyn Fullviana
(CEI.No : R25157445 l Recruit Express Pte Ltd (Healthcare & Life Science) | 99C4599
Tell employers what skills you have
Annual Reports
Clinical Research
Treatment
Healthcare
Data Entry
Clinical Trials
Protocol
Compliance
Audits
Communication Skills
Nursing
Life Sciences
Screening
Databases
IRB
Clinical Research Coordinator โข Islandwide, SG