Clinical Research Program Manager

The Lundquist Institute; Torrance (CA); On-site; USD 65,000 - 95,000; Full time

Job summary

The Lundquist Institute is seeking a Clinical Research Project Manager (CRPM) to coordinate and administer clinical trials under the direction of a principal investigator. This role emphasizes participant recruitment, data collection, regulatory compliance, and adherence to established protocols.

Responsibilities include managing study initiation through close-out, obtaining informed consent, scheduling visits, ensuring data integrity, and communicating with investigators, sponsors, and the

Qualifications

• Bachelor’s degree in life sciences, public health, or a related field.
• Experience in clinical research or healthcare (optional).
• Knowledge of clinical trial regulations and guidelines (e.g., GCP, HIPAA).
• Strong organizational and time-management skills.
• Excellent written and verbal communication skills.
• Attention to detail and ability to manage multiple tasks.

Responsibilities

• Coordinate and manage all aspects of clinical research studies from initiation to close-out.
• Recruit, screen, and enroll study participants according to protocol criteria.
• Obtain informed consent in compliance 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 (e.g., FDA, IRB, GCP).
• Monitor participant safety and report adverse events as required.
• Maintain study files, regulatory binders, and case report forms.
• Communicate with investigators, sponsors, and study team members.
• Assist with audits and inspections by regulatory agencies.

Skills

Organizational skills

Time-management

Communication skills

Attention to detail

Clinical research experience

Education

Bachelor’s degree in life sciences, public health, or a related field

Job description

Job Summary

The CRPM is responsible for coordinating and administering clinical trials under the direction of a principal investigator. This role involves participant recruitment, data collection, regulatory compliance, and ensuring that studies follow established protocols and guidelines.

Job Summary

The CRPM is responsible for coordinating and administering clinical trials under the direction of a principal investigator. This role involves participant recruitment, data collection, regulatory compliance, and ensuring that studies follow established protocols and guidelines.

Key Responsibilities

• Coordinate and manage all aspects of clinical research studies from initiation to close-out
• Recruit, screen, and enroll study participants according to protocol criteria
• Obtain informed consent in compliance 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 (e.g., FDA, IRB, GCP)
• Monitor participant safety and report adverse events as required
• Maintain study files, regulatory binders, and case report forms
• Communicate with investigators, sponsors, and study team members
• Assist with audits and inspections by regulatory agencies

Qualifications

• Bachelor’s degree in life sciences, public health, or a related field
• Experience in clinical research or healthcare (optional)
• Knowledge of clinical trial regulations and guidelines (e.g., GCP, HIPAA)
• Strong organizational and time-management skills
• Excellent written and verbal communication skills
• Attention to detail and ability to manage multiple tasks

Background and Health Clearance Required
Equal Opportunity Employer/Affirmative Action/Drug-Free Workplace