Research Analyst

• Primary point of contact for site personnel during life cycle of clinical trial
• Provides support to the Global Project Lead and CTM during project start up to ensure timely site selection and feasibility
• Ability to identify protocol deviations and pharmacovigilance issues that might affect data accuracy or patient safety
• Conduct Site qualification, site initiation, routine site monitoring close out visits (remote and onsite)
• Oversees conduct trials by reviewing study data listings, vendor dashboards, and CTMS issues/actions documentation to identify trends, errors, and any potential breeches that can impact data integrity
• Assists the Global Project Lead in identification of out-of-scope activities

Senior Clinical Research Associate – Contract

Clinical Research Associate II – Senior CRA, FSP – Cell & Gene Therapy

Clinical Research Associate II