Clinical Research Coordinator — Participant-Focused Trials

Recruit Express Pte Ltd

Singapore

On-site

SGD 30,000 - 42,000

Full time

4 days ago
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Job summary

Recruit Express Pte Ltd in Singapore is seeking a detail-oriented coordinator to support clinical research studies. You will screen participants, coordinate visits, and ensure data integrity under the study protocols and GCP guidelines.

Ideal candidates have a life sciences or health-related degree and good communication skills. Prior healthcare or research experience is preferred, and the role involves multitasking across multiple projects and liaising with investigators and stakeholders.

Qualifications

  • Degree in life sciences or related field.
  • Experience in clinical research preferred.
  • Strong organization and multitasking abilities.
  • Good communication and interpersonal skills.

Responsibilities

  • Coordinate and support clinical research studies and trials.
  • Screen and recruit suitable participants according to study protocols.
  • Collect, enter, and maintain accurate study data and documentation.
  • Schedule study visits and liaise with investigators, patients, and stakeholders.
  • Ensure compliance with study protocols, regulatory requirements, and GCP guidelines.
  • Prepare reports and assist with ethics submissions and study-related administration.
  • Manage research databases and maintain study records.

Skills

Organizational skills
Coordination
Communication skills
Interpersonal skills
Multitasking

Education

Life Sciences / Health-related degree

Job description

Recruit Express Pte Ltd in Singapore is seeking a detail-oriented coordinator to support clinical research studies. You will screen participants, coordinate visits, and ensure data integrity under the study protocols and GCP guidelines.

Ideal candidates have a life sciences or health-related degree and good communication skills. Prior healthcare or research experience is preferred, and the role involves multitasking across multiple projects and liaising with investigators and stakeholders.

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