Clinical Trial Operations Lead

LILLY CENTRE FOR CLINICAL PHARMACOLOGY PTE. LTD.

Singapore

On-site

SGD 120,000 - 180,000

Full time

8 days ago
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Job summary

Lilly Centre for Clinical Pharmacology PTE. LTD. is seeking a Study Manager to oversee clinical trial execution within the Clinical Research Unit in Singapore. The role ensures SOP/GCP compliance and acts as the primary liaison with sponsors, monitors, and ERB.

The ideal candidate brings a Diploma or Degree in Nursing, Science or health-related field with at least 5 years in clinical research, strong GCP knowledge, and proven leadership to drive study integrity and timelines.

Qualifications

  • Diploma or Degree in Nursing, Science or health-related field.
  • At least 5 years of clinical research experience.
  • Excellent GCP knowledge and study conduct experience.

Responsibilities

  • Manage study implementation from planning to closeout.
  • Liaise with sponsor and site team during protocol development for viability.
  • Lead review of study documents (protocol, consent, CRU tools).
  • Coordinate risk assessments and mitigation plans for studies.
  • Oversee maintenance of investigator trial master files and budgets.
  • Serve as liaison between CRU, sponsor, ERB and monitors.
  • Coordinate training, initiation, monitoring and close-out visits.
  • Escalate quality or performance issues and coordinate study deliveries.

Skills

GCP knowledge
Project management
Leadership
Communication
Organizational skills
Proactive
MS Office

Education

Diploma or Degree in Nursing, Science or health-related field

Tools

Microsoft Office

Job description

Lilly Centre for Clinical Pharmacology PTE. LTD. is seeking a Study Manager to oversee clinical trial execution within the Clinical Research Unit in Singapore. The role ensures SOP/GCP compliance and acts as the primary liaison with sponsors, monitors, and ERB.

The ideal candidate brings a Diploma or Degree in Nursing, Science or health-related field with at least 5 years in clinical research, strong GCP knowledge, and proven leadership to drive study integrity and timelines.

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