Clinical Research Professional

The Clinical Research Professional is responsible for site and/or project management related to clinical trials, ensuring that milestones, timelines, budgets and quality of such trials, as outlined by the study protocols, monitoring plans, SOPs, and applicable regulations and policies are met. Function: - Oversees and coordinates progress of clinical studies at the participating centers and/or clients. - Ensures that the rights and well-being of subjects are protected, that the reported study data are accurate, complete, and verifiable from source documents, and that the study is conducted in accordance with protocol, standard operating procedures, ISO/GCP and other applicable regulatory requirements. - Provides support in start-up, enrollment, follow up and closure of clinical trial activities. - Develops solutions to a variety of complex problems of diverse scope and complexity where analysis of data requires evaluation of identifiable factors. - Plans and organizes non-routine tasks w/approval. Establishes and cultivates a wide range of business relationships to facilitate completion of assignments. - May interact with vendors. - Participates in determining goals and objectives for projects. - May lead projects within the function or department and/or represents a specialized field in larger project teams. Influences middle management on business solutions. - Represents the organization as a prime contact on contracts or projects. Interacts with senior internal management and external personnel on significant matters often requiring coordination between organizations. - Uses discretion, diplomacy and tact to resolve difficult situations. May escalate serious issues to management. - Participates in the development and coaching of less experienced staff. Interested in this job? Send us your CV and motivation to: staffing@triumclinicalconsulting.com