Clinical Trial Manager

New

Skills

Clinical Research Regulatory Compliance

Job Overview

Lead planning, conduct, and oversight of operational clinical studies per protocol. Develop study documents, training materials, and trackers. Manage site feasibility, recruitment strategies, and enrollment plans. Monitor metrics and CAPA.

Responsibilities
  • Lead planning and conduct of clinical studies
  • Ensure compliance with ICH-GCP, SOPs, and regulatory requirements
  • Develop study documents and training materials
  • Drive site feasibility and recruitment strategies
  • Manage IP handling, drug accountability, and QA coordination
Requirements & Qualifications
  • Bachelor’s degree in science/health; advanced degree preferred
  • 7+ years of clinical research experience with monitoring
  • Excellent communication, interpersonal, and organizational skills
  • MS Office proficiency (Outlook, Word, Excel, PowerPoint)
  • Deep knowledge of ICH-GCP and regulatory guidelines

No forms. Your profile is generated instantly.

Job Type: Remote

Salary: Not Disclosed

Experience: Entry

Duration: 12 Months

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