Clinical Research Coordinator

Roles & Responsibilities

MAJOR DUTIES AND RESPONSIBILITIES

(A) SPECIFIC (90%)

• Liaison person with Principal Investigator (PI), site-PI and various departments for clinical research procedures e.g. Specialist Clinics, Laboratory, wards, etc.
• Plan, organise and coordinate the workflow of the research study
• Adhere to protocol procedure
• Screen research participants for eligibility according to research protocol
• Enrol research participants and ensure their compliance to research procedures
• Explain protocol to research participants and ensure that informed consent is taken as per
• International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) Guideline for Good Clinical Practice (GCP) and Human Biomedical Research Act (HBRA) requirements
• Schedule appointments for research participants within the time frame required in the protocol
• Arrange for clinical / laboratory tests and investigations; update schedule visit logs
• Draw, centrifuge blood specimens and send specimens to laboratory or store specimens in accordance with requirement of research protocol
• Assist in the completion and maintenance of biological specimen logs
• Trace and return of case notes, blood results and all other results required in the protocol.
• Assess subject’s condition; coordinate physical examinations per protocol; record medical drug history according to protocol
• Collect and maintain data, as well as provide study reports
• Maintain documentation of patient reimbursement logs, hardcopy and electronic case report forms
• Maintain investigator files and source documentation for each patient accordance to protocol requirements.
• Identify, document and submit protocol deviations to Institutional Review Board (IRB) according to research requirements
• Inform PIs, Co-Investigators, collaborators and study team members on any adjustments based on protocol change
• Complete, report and follow up on unanticipated problems involving risk to subjects and adverse events and / or serious adverse events
• Traveling to research participants’ house may be required
• Work closely with SOC clinical staff (e.g. physicians, PSAs) in clinical decision support, therapeutic interventions, and first-visit interventions.

Leadership

Mentor junior clinical research staff

Others

1. Perform quality checks on studies as Institution Monitor (where applicable)

2. Be a NHG Committee of Practice (CoP) or Faculty member in CRC Society (where applicable)

GENERAL (10%)

Tell employers what skills you have

Leadership

Microsoft Excel

Clinical Research

Treatment

Healthcare

Data Entry

Clinical Trials

Protocol

Compliance

Interventions

Team Lead

Nursing

Life Sciences

Screening

Laboratory