Clinical Research Program Manager

Job Summary

Key Responsibilities

• Cook up and administer clinical trials under the principal investigator's guidance.
• Recruit, screen, and enroll study participants according to protocol criteria.
• Obtain informed consent in line with ethical and regulatory standards.
• Schedule and conduct study visits, procedures, and follow-ups.
• Collect, record, and maintain accurate study data and source documentation.
• Ensure compliance with study protocols, institutional policies, and regulatory requirements.
• Monitor participant safety and report adverse events as needed.
• Maintain study files, regulatory binders, and case report forms.
• Communicate with investigators, sponsors, and study team members.
• Aid with audits and inspections by regulatory agencies.

Qualifications

• Acquire a bachelor’s degree in life sciences, public health, or a related field.
• Gain experience in clinical research or healthcare (optional).
• Develop knowledge of clinical trial regulations and guidelines (e.g., GCP, HIPAA).
• Build strong organizational and time-management skills.
• Enhance your written and verbal communication abilities.
• Exercise attention to detail and handle multiple tasks simultaneously.

Make sure your application is complete and signed; incomplete submissions won't be considered. Background and Health Clearance Required. Equal Opportunity Employer/Affirmative Action/Drug-Free Workplace.