Clinical Research Quality & Governance Lead

Recruit Express Pte Ltd

Singapore

On-site

SGD 90,000 - 130,000

Full time

4 days ago
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Job summary

Recruit Express Pte Ltd is seeking a Sr/Assistant Manager to support institutional research governance within the Clinical Research & Innovation Office in Singapore. The role focuses on maintaining research integrity and quality across clinical research activities, with responsibilities spanning monitoring visits, compliance checks, audits, regulatory submissions, and data reporting.

Candidates should have a life sciences or healthcare degree and hands-on experience with ICH-GCP E6, IRB

Qualifications

  • Relevant degree in Life Sciences, Pharmacy, Nursing, or healthcare related field.

Responsibilities

  • Conduct study monitoring visits and review study documentation, assess protocol adherence and support study teams to improve quality.
  • Conduct compliance checks across research operations, identify gaps, provide feedback and recommendations.
  • Support institutional audits, inspections and accreditation activities.
  • Identify gaps and drive improvement initiatives to enhance quality of research studies and strengthen internal processes.
  • Support sponsor oversight responsibilities and institutional quality management of clinical trials to ensure compliance with sponsor obligations and regulatory requirements.
  • Provide regulatory advice and liaise with internal stakeholders for timely regulatory submissions.
  • Drive outreach activities to educate staff and research teams to promote proper conduct of research.
  • Collect and compile data for management reporting.
  • Manage operations of institutional research governance and administration.

Skills

Monitoring studies
ICH-GCP knowledge
Regulatory liaison

Education

Life Sciences degree

Job description

Recruit Express Pte Ltd is seeking a Sr/Assistant Manager to support institutional research governance within the Clinical Research & Innovation Office in Singapore. The role focuses on maintaining research integrity and quality across clinical research activities, with responsibilities spanning monitoring visits, compliance checks, audits, regulatory submissions, and data reporting.

Candidates should have a life sciences or healthcare degree and hands-on experience with ICH-GCP E6, IRB

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