Clinical Research Coordinator, Well Clinic

National University Polyclinics; Singapore; On-site; SGD 40,000 - 60,000; Full time

Job summary

A healthcare organization in Singapore is seeking a Clinical Research Coordinator to manage research projects focused on frailty and aging. The role involves participant recruitment, data management, and coordination with stakeholders. Ideal candidates should have a Bachelor's degree in health sciences, project management experience, and strong communication skills. Interested applicants can apply via email at [e-mail].

Qualifications

• Bachelor's degree in health or life sciences, nursing or related field or equivalent.
• Prior work experience in clinical trials is an advantage.
• Able to coordinate and dispatch biological specimens.

Responsibilities

• Assist in recruiting, screening, and taking consent from study participants.
• Handle entry and validation of study data.
• Coordinate scheduling and visits for stakeholders.

Skills

Excellent time-management

Communication skills

Proficient in MS Office applications

Ability to work independently

Teamwork

Education

Bachelor's degree in health or life sciences

Diploma in health or life sciences

Tools

NGEMR EPIC

REDCap

Job description

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Clinical Research Coordinator, Well Clinic

Job ID: 8614

Job Function: Allied Health

Overview*

The incumbent will work closely with the Principal Investigator and study team members to ensure the successful timely completion of the research project related to (but not limited to) frailty and ageing. The incumbent’s principal role involves project management, recruitment, data collection, data entry and analysis. He/she may be required to liaise with personnel from partnering institutions in the course of his/her work.

Job Responsibilities*

You will be responsible for the following:

• Assist the investigators to recruit, screen, take consent and follow up participants of the study, in strict adherence to the study protocol and other applicable regulatory and ethical requirements.
• Coordinate collection and dispatch of biological specimens, and monitoring of adverse events and safety reporting.
• Handle entry and validation of study data, extraction of relevant information from medical records, reporting of adverse events, maintenance of investigators files and other essential documentation.
• Prepare and sort information before entering data into database and maintain data entry accuracy and quality levels to support team productivity and efficiency.
• Resolve incomplete information and data discrepancies.
• Coordinate scheduling and visits for stakeholders and study participants, as well as related finances (such as reimbursements) and logistics.
• Support in other functions such as general administration or coordination as required.

Requirements*

• Bachelor's degree in health or life sciences, nursing or related field or equivalent OR Diploma in health or life sciences, nursing or related field or equivalent with minimum 3 years working experience

as CRC

• Prior work experience in clinical trials and/or project management in healthcare will be an advantage
• Excellent time-management and communication skills
• Able to work independently and as a team
• Proficient in hospital databases (NGEMR EPIC), MS Office applications (Word, Excel & Powerpoint) and research databases (REDCap)

If the role sounds interesting to you, please contact ‘[e-mail]’ to understand more on the role. Please indicate the position that you are interested in the subject heading.

*Only Singapore Citizens and Singapore Permanent Residents may apply.