Clinical Research Associate (los Angeles Based)

ProPharma Group

Los Angeles, California, United States
Hybrid
Clinical trial monitoring experience
Proficiency in data management
Understanding of regulatory compliance
ProPharma has been improving patient health for over 20 years by empowering biotech and pharmaceutical organizations

Job Summary

  • ProPharma has been improving patient health for over 20 years by empowering biotech and pharmaceutical organizations.
  • The role involves executing and managing clinical study plans and ensuring compliance with protocols.
  • ProPharma values diversity, equity, and inclusion, encouraging employees to be their authentic selves.

Matching Summary

ProPharma has been improving patient health for over 20 years by empowering biotech and pharmaceutical organizations.

Skills & Requirements

Must-have

  • Clinical trial monitoring experience
  • Proficiency in data management
  • Understanding of regulatory compliance

Nice-to-have

  • Experience in In Vitro Diagnostics
  • Strong on-site monitoring experience
  • Knowledge of electronic trial master file systems

Key Requirements

  • Bachelor’s Degree or equivalent experience
  • 4+ years clinical research monitoring experience
  • Authorization to work in the United States

Work Rights

Not specified

Tailored Resume

Cover Letter