Clinical Trials Project Manager at SECOND TALENT SG PTE LTD
Singapore, , Singapore -
Full Time


Start Date

Immediate

Expiry Date

14 Nov, 25

Salary

6500.0

Posted On

14 Aug, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Biomedical Engineering, Coordination Skills, Regulatory Documentation, Clinical Trials, Life Sciences, Public Health, Dentistry

Industry

Pharmaceuticals

Description

We are representing a confidential, fast-growing company at the forefront of dental AI innovation . The company is developing a revolutionary AI-powered screening device/software aimed at transforming early detection and diagnosis in oral healthcare.
To support product validation and global market entry, we are seeking a Clinical Trials Project Manager to lead and manage clinical studies from initiation to close-out.

REQUIREMENTS

  • Bachelor’s degree or higher in Life Sciences, Biomedical Engineering, Dentistry, Public Health, or a related field
  • 3–5 years’ experience managing clinical trials, preferably in medical/dental devices or digital health/AI
  • Strong understanding of GCP and relevant regulatory frameworks
  • Experience with investigator-initiated trials, device/software validations, or real-world data studies is a plus
  • Excellent project management and stakeholder coordination skills
  • Strong written and verbal communication, especially in technical and regulatory documentation
  • Familiarity with dental or radiology clinical environments is advantageous
  • Ability to manage multiple priorities in a fast-paced, startup-like environment
Responsibilities
  • Lead and manage end-to-end clinical trial activities (planning, execution, monitoring, and reporting) in alignment with GCP, regulatory requirements, and project timelines
  • Collaborate with cross-functional teams including R&D, regulatory affairs, QA, and data science to ensure study objectives are met
  • Oversee the selection, initiation, and coordination of clinical trial sites, investigators, and vendors
  • Prepare and maintain all clinical trial documentation (protocols, informed consent forms, CRFs, study reports)
  • Monitor trial progress, manage budgets and timelines, and mitigate risks proactively
  • Ensure compliance with all applicable ethical and regulatory standards including IRB/IEC submissions
  • Coordinate data collection and validation in conjunction with the AI/tech team for real-world performance benchmarking
  • Report trial milestones and results to internal leadership and external regulatory bodies
Loading...