Clinical Research Associate (CRA) - Remote

Overview

In this contract CRA role, you will be responsible for monitoring the progress of clinical studies (primarily, our phase 3 Precision-T study), either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.

In Short

• Monitor clinical studies progress
• Conduct site visits and remote monitoring
• Ensure compliance with protocols and SOPs
• Work primarily on the phase 3 Precision-T study
• Travel expected: ~1+ site visit per week
• Preferred location: West Coast, USA
• Contract position
• Work can be done remotely
• Focus on blood cancer treatments
• Join a late-stage biotechnology company

Requirements

• Experience in clinical research
• Knowledge of ICH-GCP guidelines
• Ability to conduct site visits
• Strong communication skills
• Detail-oriented and organized
• Ability to work independently
• Familiarity with regulatory requirements
• Experience with remote monitoring
• Understanding of blood cancer treatments
• Flexibility to travel as needed

Benefits

• Opportunity to work in a meaningful field
• Flexible work environment
• Engage with innovative cell therapies
• Collaborate with a dedicated team
• Contribute to improving patient outcomes
• Gain experience in a late-stage biotechnology company
• Potential for professional growth
• Work remotely from anywhere in the U.S.
• Competitive contract compensation
• Access to industry-leading research