Clinical Operations Manager I

We are looking for an experienced Clinical Operations Manager I to join our team! Are you well organized, but adaptable to unexpected changes? Someone who is able to see the bigger picture, without losing sight of the day-to-day tasks? If the answer is yes, keep reading! This role is ideal for an individual who can motivate teams to do great work collaboratively in order to produce the best quality outcomes possible. In this position you will: Manage site identification and evaluation. Develop or review essential study documents including protocols, case report forms (CRFs), source documents, project management plans, monitoring plans, reference tools, and study manuals. Review site regulatory documents for compliance with CPC Standard Operating Procedures (SOPs) and applicable laws, regulations, and guidelines and to facilitate approval of investigational product release. Prepare central IRB submissions and resolve IRB issues. Manage site enrollment and study subject tracking and payments. Assist with the monitoring of project deliverables and project timelines. Develop and distribute project documents (e.g. safety reports, lab reports, deviations reports, monitoring reports, follow-up letters, meeting minutes, newsletters, and regulatory documents) Identify project-specific training for team members and notify appropriate designee to ensure completion and filing of training documentation. Provide investigational product or device tracking and disposition as required by project. Develop and manage site and vendor contracts including investigational product (IP) supply, interactive voice/web response system, electronic data capture system, core labs and other applicable clinical services. Track and approve vendor payments. Manage multidisciplinary project team members in relation to their role on assigned projects. Proactively identify issues and discuss resolutions with applicable department heads, project team, CPC executives and/or the sponsor. Track implementati