Clinical Research Associate I/ Clinical Research Associate II

📋 Description

• • As a Clinical Research Associate I/II at Precision for Medicine, you will play a critical role in advancing oncology and rare disease therapies by ensuring clinical trials are conducted with the highest standards of quality, compliance, and patient safety. Your work directly contributes to bringing life-saving treatments to patients through meticulous site monitoring and protocol adherence.
• • Day to day, you will monitor and own the progress of clinical studies at investigative sites, conduct site visits (pre-study, initiation, routine, and close-out), verify source data, ensure regulatory documentation is complete and accurate, identify and mitigate study risks, and serve as the primary liaison between sites and the project team. You will also assist in study setup activities, prepare for investigator meetings, and maintain timely and accurate trial master files.
• • You will join a passionate, retention-focused CRO that values employee voice, work-life balance, and professional growth. Precision for Medicine fosters a supportive environment where CRAs are empowered to make meaningful contributions, receive direct management support, and thrive in a culture that prioritizes both scientific excellence and personal well-being.
• • In this role, you will deepen your expertise in oncology clinical research, become a protocol expert on one to two studies, refine your risk-based monitoring and problem-solving skills, and gain experience in a dynamic, innovative CRO that integrates advanced biomarker and data analytics into trial design—positioning you for long-term growth in clinical research and precision medicine.