Research Analyst

• Primary point of contact for site personnel during the life cycle of clinical trial
• Study start up support, site activation, trial conduct and closeout of a clinical trial
• Provides support to the Global Project Lead and CTM during project start up
• Assists with collection of essential documents from the site
• Ability to identify protocol deviations and pharmacovigilance issues
• Conduct Site qualification, site initiation, routine site monitoring close out visits
• Expert documentation of monitoring priorities/activities
• Oversees conduct trials by reviewing study data listings, vendor dashboards, and CTMS issues/actions documentation
• Ability to present essential function of CRA role in Bid Defenses, Investigator Meetings, and Sponsor Face to Face meetings
• Provides support to the CTM and Global project lead in negotiation of site budgets and contracts

Senior Clinical Research Associate – Contract

Senior Clinical Research Associate I

Senior Clinical Research Associate – FSP