Clinical Trials Manager

New

Skills

Budgeting and Forecasting Clinical Data Management Clinical Research Management FDA Regulations ICH-GCP Guidelines Investigator Selection MS Office Suite Protocol Development Regulatory Compliance Vendor Management

The Clinical Trials Manager will oversee the execution of complex clinical studies, ensuring they meet timelines, budgets, and quality standards. This role involves selecting and managing vendors and CROs while maintaining compliance with regulations. The successful candidate will lead the preparation of protocols, consent forms, and investigator training, collaborating closely with Clinical Data Management.

Key Responsibilities
  • Manage execution of clinical studies.
  • Select and oversee vendors/CROs.
  • Oversee contracting, budgeting, and payments.
  • Lead protocol and consent preparation.
  • Collaborate with Clinical Data Management for data accuracy.
  • Train CROs, vendors, and staff on protocols.
Required Skills & Qualifications
  • Bachelor's in life sciences; advanced degree preferred.
  • 8+ years in clinical research, 4+ years leading trials.
  • 4-7 years supporting trials in regulated environments.
  • Experience managing CROs.
  • Knowledge of FDA regulations and ICH-GCPs.
  • Proficient in MS Office Suite.
  • Strong organizational and leadership skills.

No forms. Your profile is generated instantly.

Job Type: Remote

Salary: Not Disclosed

Experience: Entry

Duration: Months

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