Roles & Responsibilities
Work Hours : Monday to Friday, 8 : 00AM to 4 : 30PM, and Saturday, 8 : 00AM to 12 : 30PM, are required.
Salary : Up to 3400
Job Scope :
- Be involved in subject recruitment, scheduling and data entry. Screen patients based on study eligibility, and communicate the study aims to potential subjects in layman terms.
- Obtain consent taking, administer study questionnaires and follow-up on study participants.
- Work closely with research team, clinicians, clinic staff and other relevant internal departments to ensure research study needs are met.
- Able to work on tight timelines, set sensible targets and achieve research deliverables.
- Conduct research study activities like patient recruitment, data collection and data management.
- Assist in data collection from electronic health records.
- Set up and maintain study investigator files, including records of consent taken and blood collection.
- Maintain study records in databases
- Responsible for maintaining strict adherence to research protocols
- Liaise with investigators, clinicians and laboratory team to set up clinical workflows at multiple clinical departments for research recruitment.
- Prepare necessary documentation for audit purposes.
- Coordinate the submission of new IRB applications, study amendments and annual reports.
- Maintain the highest standard of professional conduct and record keeping in accordance with policies, ethics requirements and local regulations.
- Assist with any other duties of a similar nature that are delegated by the PI.
Job Requirement :
Min Degree in Science / Public Health / Social ScienceAble to start work immediately or within a short noticeInterested candidates, do submit your resume to : wendykhoo@recruitexpress.com.sg
Wendy Khoo Hui Wen (R1761775)
Recruit Express Pte Ltd
Company EA Licence number : 99C4599
Tell employers what skills you have
Annual Reports
Clinical Research
Theatre
Public Health
Healthcare
Data Management
Data Entry
Clinical Trials
Protocol
Nursing
Life Sciences
Screening
Scheduling
Laboratory
Audit
IRB