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Job Details
Lead Clinical Research Associate
Permanent
Job Specifications & Responsibilities Performs all aspects of study site management including routine monitoring and close-out of clinical sites, maintenance of study files, conducts pre-study and initiation visits, liaison with other vendors. Prepares accurate and timely trip reports, administration of clinical research projects, recruiting investigators, collecting investigator documentation, site management and preparation of monthly status reports Assists in managing project budget and investigator site budget, attend project team meetings, plan and attend investigator meetings. Assists in preparing/reviewing protocols and design of case report forms and other study documentation in collaboration with the project manager Develops site specific communication plan focusing on early feedback to the sites and proactive management of performance criteria and measures Develops and maintains strong working relationships with investigators and study site staff, promoting patient recruitment strategies Education & Experience: Science or relevant degree Minimum 2 years Clinical Research Associate experience
