Clinical Research Coordinator, Investigational Medicine Unit (Contract)

Singapore National Eye Centre; Singapore; On-site; SGD 40,000 - 80,000; Full time

Job summary

Join a forward-thinking organization as a Clinical Research Coordinator in an innovative clinical trial environment. This role involves managing clinical trials, ensuring compliance with regulatory standards, and providing essential support in research activities. You will engage with research subjects, monitor their well-being, and maintain accurate records, contributing to groundbreaking medical research. If you are a proactive team player with a passion for clinical research and possess the ability to educate and counsel subjects, this is an exciting opportunity to make a meaningful impact in the field of medicine.

Qualifications

• 3+ years of experience in clinical research coordination.
• Knowledge of regulatory guidelines, ICH-GCP.

Responsibilities

• Manage clinical trials and ensure compliance with regulatory guidelines.
• Interview research subjects and monitor their well-being.

Skills

Interpersonal Skills

Team Collaboration

Problem Solving

Patient Education

Education

Degree in Life Sciences

Diploma in Nursing

Tools

MS Office Word

MS Office Excel

Job description

Clinical Research Coordinator, Investigational Medicine Unit (Contract)

Job Category: Research

Posting Date: 15 Mar 2025

Job Description:
You will work in an early phase clinical trial environment that facilitates clinical research studies, academic and educational activities. You will provide research support service in clinical trials and ensure the delivery of trial-related services that comply with regulatory guidelines, i.e. ICH-GCP. Other key responsibilities include managing the clinical trial(s), administration of clinical trial materials and performing trial-related duties and/or medical procedures in accordance to requirements stipulated by the trial or as assigned.

You will be involved in planning and executing clinical trials through interviewing research subjects, explaining study procedures, monitoring the subjects’ well-being and recording the subjects’ medical history. You will also perform various clinical trial procedures such as collecting and processing biological specimens, collating data and maintaining proper records of reports and related documents.

We regret that only shortlisted candidates will be contacted.

Job Requirements:

1. Degree in Life Sciences or Diploma in Nursing;
2. Preferably attended the Good Clinical Practice (GCP) Programme or a similar course;
3. Minimum 3 years’ relevant experience in clinical research coordination;
4. Ability to educate and counsel research subjects and possess good interpersonal skills;
5. Team-player, proactive and able to pre-empt potential obstacles and provide solutions within timelines;
6. Proficiency with MS Office Word and Excel;
7. Must be fully vaccinated against COVID-19.