Clinical Research Associate II

Summary

Join Precision for Medicine, a unique CRO integrating clinical trial execution with scientific knowledge and advanced data sciences. We offer a supportive culture with high CRA retention, reasonable travel, and work-life balance. You'll be a protocol expert, have a voice in decision-making, and contribute to life-changing therapies. We value your contributions and provide opportunities for growth and development. Your responsibilities will include monitoring clinical studies, coordinating activities, and interacting with clients. We are seeking experienced CRAs with oncology expertise.

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
• Support Project Managers with trials that are larger in scope
• Train and mentor junior staff members
• Interact directly with clients
• Initiate payments
• 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