Job Overview
Clinical research associates play a vital role in the success of clinical trials. As a CRA, you will be responsible for managing and monitoring clinical studies from initiation to close-out.
Key Responsibilities
* Conduct site visits to evaluate study sites for eligibility and ensure high-quality data collection on time.
* Evaluate and track study recruitment progress, monitor visit reports, and maintain documentation records throughout the study lifecycle.
* Collaborate with principal investigators to ensure compliance with safety reporting requirements and regulatory standards.
Required Qualifications:
* Bachelor's degree in medical, pharmacology, or biology related field.
* At least one year of CRA experience with good clinical practice knowledge and skills in Microsoft Office applications.
About This Role
This is an exciting opportunity for professionals seeking to advance their careers in clinical research. Our team is dedicated to delivering high-quality services and fostering a collaborative environment that promotes growth and development.
Why Join Us?
We offer a dynamic work environment that values innovation, teamwork, and excellence. As a CRA, you will have opportunities to develop your skills, build meaningful relationships, and contribute to the success of our clinical trials.