Posted:
June 16, 2026
Location:
singapore, singapore, Singapore

Job Description

Responsibilities:

  • Assist in the planning and execution of clinical research studies.
  • Coordinate and oversee the collection, analysis, and interpretation of study data.
  • Ensure compliance with study protocols, regulatory requirements, and ethical standards.
  • Conduct site visits to monitor study progress and ensure adherence to study procedures.
  • Manage study documentation, including case report forms and informed consent documents.
  • Collaborate with study investigators and study team members to ensure smooth study operations.
  • Conduct training sessions for study site personnel on study procedures and requirements.
  • Prepare study reports and contribute to the development of study protocols and study-related documents.
  • Stay updated on relevant regulations, guidelines, and industry best practices in clinical research.
  • Bachelor's degree or above in Life Sciences, Pharmacy, or a relate...

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Job Overview

Job Type: Full-time
Location: singapore, Singapore
Posted: June 16, 2026
Deadline: July 26, 2026