Clinical Study Associate
4 days ago
Job Summary:
- 6 month contract (renewable)
- Salary: Basic Up To $3400
- Location: West, Queenstown
- Working Hours: Mon to Fri (8AM to 4.30PM), and Saturday (8AM to 12.30PM)
Job Responsibilities:
1) Subject Recruitment and Follow-Up
- 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.
2) Research Documentation / Administrative duties
- 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 such as Redcap and in electronic health record systems.
- Responsible for maintaining strict adherence to research protocols i.e., HBRA.
- 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 hospital policies, ethics requirements and local regulations.
- Assist with any other duties of a similar nature that are delegated by the PI.
Job Requirements:
- Bachelor Degree in Science/ Public Health/Social Science. No experience is welcome (but candidates with relevant experience will have an advantage)
- Able to adapt in a fast-paced environment, with a strong focus to meet research deliverables and targets.
- Strong interpersonal and communication skills. Leadership and accountability to tasks is very desirable.
- Independent and mature. Able to work independently, as well as in a team.
- Meticulous, well-organized and able to multi-task
- Ability to work in an interdisciplinary environment with different groups of stakeholders.
- Willing to travel between the Hospitals and external study sites as part of his / her work.
- Knowledge of Good Clinical Practice (GCP) guidelines and the Human Biomedical Research Act (HBRA)
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Elis Wong Wai Yan
Registration Number: R
EA Licence No: 06C2859 (MCI Career Services Pte Ltd)
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