Job Description

JOB SUMMARY:

Responsible for overall clinical study management, including planning, communication, coordination, and execution of tasks for the studies. This role will ensure all clinical studies are conducted in compliance with regulatory requirements and organizational standards.

Key Responsibilities:

• Plan, coordinate, and manage all aspects of clinical studies
• Coordinate Ethical Committee and Institutional Review Board notifications
• Create, maintain, and oversee study files and archiving
• Manage selection and oversight of testing laboratories for the studies
• Manage clinical research organizations and ensure proper monitoring of studies, data collection, and data handling
• Prepare, revise, and maintain procedures for conducting clinical studies

Required Qualifications:

• Bachelor's or Masterâs Degree in Life Sciences or a related field
• 3 to 5+ years of relevant experience in clinical study management
• Strong knowledge of clinical research regulations and guidelines
• Excellent organizational, communication, and documentation skills
• Ability to work with cross-functional teams and external vendors

Education:

Bachelor's or Masterâs Degree in Life Sciences or related field

Experience:

3 to 5+ years of relevant experience in clinical research or study management

Certifications:

Post-graduate certification and/or license may be required (if applicable)

Job Tags

Full time,

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