Remote Clinical Research Associate II

Summary

Join Precision for Medicine, a unique CRO that combines clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences. As a CRA, you will focus on lower-than-average protocols, enjoy reasonable travel, and have a great work-life balance. Your voice will be heard in our smaller company, where you can influence and impact decisions.

Requirements

• 4-year college degree or equivalent experience
• CRA experience within the CRO or pharmaceutical industry; 2+ years for a CRA II and 3+ years for Senior CRAs
• Oncology experience is essential
• Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions)

Responsibilities

• Monitor and own the progress of clinical studies at investigative sites
• Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards
• Coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.)
• Handle appropriately sized clinical trials, and support Project Managers with trials that are larger in scope
• Train and mentor junior staff members
• Interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations

Preferred Qualifications

• Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline
• Two+ years of oncology experience
• Study start up activities experience
• For Senior CRAs, understanding of financial management