Senior / Clinical Research Coordinator

**Job Title**: Senior/ Clinical Research Coordinator (SCRI)

**Department**: SCRI

**Business Entity**: SCRI

**Overview**

The Consortium for Clinical Research and Innovation, Singapore (CRIS) brings together five national
R&D, clinical translation and service programmes to advance clinical research and innovation for
Singapore, and establish important capabilities for a future-ready healthcare system.
The Business Entities under CRIS include:
Singapore Clinical Research Institute (SCRI)

National Health Innovation Centre (NHIC)

Advanced Cell Therapy and Research Institute, Singapore (ACTRIS)

Precision Health Research, Singapore (PRECISE)

Singapore Translational Cancer Consortium (STCC)

Cardiovascular Disease National Collaborative Enterprise (CADENCE)

Together, CRIS makes a positive difference to Singapore patients and researchers by ensuring that
these clinical research platforms and programmes are at the cutting edge of capability development
and innovation. If you are as passionate as we are in clinical trials and research, we want you

**SCRI**

The Singapore Clinical Research Institute (SCRI) is the national academic research organisation
dedicated to enhancing the standards of clinical research, and coordinating clinical trials. Our
mission is to spearhead and develop core capabilities, infrastructure and scientific leadership for
clinical research in Singapore. SCRI also works with the National Medical Research Council
(NMRC) to assist the Ministry of Health (MOH) in implementing clinical trials policy and strategic
initiatives to support and develop clinical research competencies locally. In driving towards its
vision, SCRI collaborates with clinicians to enhance Singapore’s clinical research and strengthen
its expertise in executing multi-site, multi-national studies and the development of regional clinical
research networks.

**What you will be working on**

**The Role**:
The Sr/Clinical Research Coordinator will be based in a public healthcare institution to support
the early phase clinical trials

You will be involved in Early Phase Clinical Trials (Pharmaceutical Sponsored and Investigator
Initiated Study), which includes coordinating clinical research activities from study start-up,
screening and recruiting/enrolling patients till the study closure, which includes but not limited to:
Develop and implement study workflow, documents, materials and tools in accordance to the
research protocols
Assist in liaising and preparation of the IRB and/or regulatory documents for submission

Coordinate screening, recruitment, follow-up visits and study procedures in accordance to
the research protocols, ICH-GCP and institution polices
Perform specimen collection, processing, labelling, storage and dispatch (e.g. blood, urine,
stool, tissues, Conduct vital signs monitoring and ECG recording
Maintain the Investigator Site Files and ensuring all documentation / records are accurate,
complete and up-to-date
Manage the investigational product (device, drugs, pharmaceuticals) which includes proper
storage, documentation, dispensing, accountability, and labelling of drugs in accordance to the
ICH-GCP guidelines and regulatory requirements
Ensure the laboratory and diagnostic reports are available and reviewed in a timely manner
Perform serious adverse events reporting
Attend various meetings (eg.investigator’s meeting (local / overseas), site initiation / periodic/
close-out meetings)
Serve as the primary point of liaison and coordination between stakeholders, assist in
responding to any audit findings and implement changes
Prepare the necessary billing documents to sponsors and/or other relevant stakeholders and
monitor the financial aspects of the research study

**What we are looking for**

At least a bachelor degree in life sciences, health sciences, nursing, pharmacy and/or related
disciplines

A team player with excellent communication and writing skills
Strong organizational, time management and problem-solving skills, Proficient in Microsoft

**What you need to know