Clinical Research Coordinator - Up $3400 / Central / Govt Hospital - C.L

MCI CAREER SERVICES PTE. LTD.; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading research organization in Singapore is seeking candidates for a role involving subject recruitment, data entry, and coordination of research study activities. The ideal candidate will hold a Bachelor’s degree in a relevant field and possess good communication skills. Responsibilities include maintaining research protocols and supporting data collection. This position offers the opportunity to work closely with a diverse research team in the healthcare sector.

Benefits

Government healthcare benefits

Competitive salary

Qualifications

• Bachelor degree in a relevant field is essential.
• Strong communication and interpersonal skills required.
• Proficiency in Microsoft Office applications is a must.

Responsibilities

• Manage subject recruitment and follow-up processes.
• Conduct data collection and data management for research.
• Ensure adherence to research protocols and documentation standards.

Skills

Good communication skills

Interpersonal skills

Proficient in Microsoft Office

Education

Bachelor Degree in Science/Public Health/Social Science

Job description

Benefits Summary

• Government Healthcare Sector
• Up $3400
• Office hours

Job Responsibilities

• 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.
• 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.

Requirements

• Bachelor Degree in Science/ Public Health/ Social Science
• Good communication and interpersonal skills.
• Proficient in Microsoft office applications.

Applicants who possess relevant experience for the above responsibilities are most welcome to apply. If you do not possess the above experience, your application will still be considered on individual merits and you may be contacted for other opportunities.

Interested candidates kindly click the APPLY NOW button.

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We regret to inform that only shortlisted candidates would be notified.