Clinical Research Coordinator, Investigational Medicine Unit

Singapore General Hospital; Singapore; On-site; SGD 50,000 - 70,000; Full time

Job summary

A prominent healthcare institution in Singapore seeks a Clinical Research Coordinator to manage early phase clinical trials and ensure compliance with regulatory guidelines. The ideal candidate will have a degree in Life Sciences or a Diploma in Nursing and a minimum of three years of relevant experience. Responsibilities include interviewing subjects, providing education, and managing clinical trial procedures effectively within timelines. Excellent interpersonal skills and proficiency in MS Office are essential for success in this role.

Qualifications

• Minimum 3 years’ relevant experience in clinical research coordination.
• Preferably attended the Good Clinical Practice (GCP) Programme or a similar course.

Responsibilities

• Manage clinical trial(s) and ensure compliance with regulatory guidelines.
• Interview research subjects and explain study procedures.
• Perform various clinical trial procedures, collect and process biological specimens.

Skills

Educate and counsel research subjects

Interpersonal skills

Team collaboration

Proactivity in problem-solving

Proficiency with MS Office

Education

Degree in Life Sciences or Diploma in Nursing

Job description

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

• Degree in Life Sciences or Diploma in Nursing
• Preferably attended the Good Clinical Practice (GCP) Programme or a similar course
• Minimum 3 years’ relevant experience in clinical research coordination
• Ability to educate and counsel research subjects and possess good interpersonal skills
• Team‑player, proactive and able to pre‑empt potential obstacles and provide solutions within timelines
• Proficiency with MS Office Word and Excel