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Job #02547

About our client Our client is a world-leading healthcare company that has developed a reputation for successfully bringing impactful products to market in a variety of therapeutic areas. With an experienced clinical team and empowering corporate culture that is focused on the professional development of its employees, this is a great opportunity for the right candidate! Position Location Lead Clinical Research Associate New Jersey Salary Highly competitive package, commensurate with experience Responsibilities 1) Manage all aspects of monitoring and site management for assigned clinical investigator sites and assigned trials 2) Assess clinical investigator site processes and suitability of site facilities 3) Manage all site-related activities from site selection to close out and ensure that study execution is on track 4) Prepare site audits and regulatory inspections to ensure successful outcome 5) Manage internal/external study budgets 6) Assess site performance, processes and qualification of staff to ensure adherence to study protocol, regulatory and local legal requirements 7) Serve as a role model and mentor for less experienced monitors on process, technical skills and behavioral competencies 8) Contribute to improve the working practices 9) Train and supervise cross functional site personnel on study protocol and procedures for the duration of the study Requirements 1) BA/BS degree or equivalent combination of education and experience in a scientific discipline 2) 3-5 years of monitoring experience 3) Minimum 1-year experience as a Lead CRA 4) Significant technical, medical or industry experience in a clinical research setting 5) Working knowledge of Good Clinical Practices 6) Ability to multitask and work effectively in a fast-paced environment 7) Strong organizational skills 8) Strong written/verbal communication and diplomacy skills