Clinical Research Coordinator, Investigational Medicine Unit (2 year contract)

SingHealth Group; Outram; On-site; CAD 60,000 - 80,000; Full time

Job summary

A healthcare organization in Canada, Nova Scotia is seeking a Clinical Research Coordinator for a 2-year contract. The role involves supporting clinical trials, ensuring compliance with regulatory guidelines, and managing trial procedures. Candidates should have a degree in Life Sciences or Diploma in Nursing, with at least 3 years of relevant experience. Proficiency in MS Office and good interpersonal skills are essential for success in this role.

Qualifications

• Minimum 3 years’ relevant experience in clinical research coordination.
• Ability to educate and counsel research subjects.

Responsibilities

• Provide research support service in clinical trials.
• Ensure delivery of trial-related services complying with regulations.
• Plan and execute clinical trials, monitor subjects’ well-being.

Skills

Good interpersonal skills

Team-player

Proactive problem-solving

Proficiency with MS Office

Education

Degree in Life Sciences or Diploma in Nursing

Good Clinical Practice (GCP) Programme

Job description

Clinical Research Coordinator, Investigational Medicine Unit (2 year contract)

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

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