Data Management Coordinator (Clinical Trials Office)

Singapore National Eye Centre; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading company in clinical research is looking for a Data Management Coordinator to join its Clinical Trials Office. This role involves assisting with data management in clinical trials, ensuring compliance with protocols, and maintaining study databases. The ideal candidate will have relevant qualifications and experience, strong communication skills, and an ability to work independently across multiple projects.

Qualifications

• Bachelor’s degree required.
• At least 2 years of relevant experience.
• Cancer research background is an advantage.

Responsibilities

• Assist in data entry for clinical trials and manage data discrepancies.
• Support feasibility studies and reporting of safety updates.
• Maintain and update feasibility databases and assist with CRF design.

Skills

Excellent written and verbal communication skills

Good organizational skills

Interpersonal skills

Proficient in Microsoft Office

Ability to complete tasks independently

Understanding of medical and clinical research terminology

Education

Bachelor’s Degree in Life Science, Biomedical Science, or related field

Job description

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National Cancer Centre of Singapore Pte Ltd

Data Management Coordinator (Clinical Trials Office)

Job Category: Research

Posting Date: 26 May 2025

We are looking for a driven Data Management Coordinator (DMC) to join the Clinical Trials Office team! The DMC will assist in data entry of studies and help resolve data discrepancies, ensuring that study data are recorded in accordance with the protocol, Good Clinical Practice (GCP) Guidelines, all applicable regulatory requirements and the Clinical Trials office’ Standard Operating Procedures.

Key Responsibilities:

1. Filling of case report forms for both sponsored trials and IITs

• Enter research patient data into paper case report forms and various electronic data capture systems.
• Assist CRCs in answering data queries.
• Attend Site Initiation Meeting and site audits and inspections.
• Assist CRCs in reporting SAEs and safety updates.

2. Reporting SAEs and safety updates

• Assist CRCs in reporting SAEs and safety updates Eg. SUSARs. Reporting of safety updates and SAEs must be in accordance with the protocol, sponsor, SGGCP, IRB and HSA requirements.

3. Feasibility Exercises

• Assist in feasibility exercises conducted by trial sponsors.Ensure NDAs executed before exchanging confidential information.
• Ensure timely correspondences with sponsors and timely reply on feasibility exercises.
• Maintain and update feasibility database.
• File and safe keep feasibility documents.
• Assist the DM Team with CRF design as and when necessary.

5. Study database creation

• Work closely with the data manager to ensure that study databased are completed in time for SIV.

6. Data Discrepancy Management

• Ensure data entered is clean and free from discrepanies.

7. Other duties

• As assigned by the supervisor and may include the following:
• Assist investigators to register and maintain trials in the clinicaltrials.gov database.
• Assist CRCs to apply for HSA or IRB application whenever necessary.

Key Requirements:

• Bachelor’s Degree in Life Science, Biomedical Science, or a related field
• At least 2 years of prior working experience in similar job scope
• Excellent written and verbal communication skills
• Good organizational and interpersonal skills
• Proficient in Microsoft Office & Powerpoint
• Self-motivated and a team player
• Ability to complete tasks independently with minimal supervision
• Ability to work on multiple projects involving multiple stakeholders concurrently
• Possess an understanding of medical and clinical research terminology
• Cancer research background will have added advantage