Clinical Operations Manager
(ID: 2026-3199) Axle is a bioscience and information technology company that offers advancements in translational research, biomedical informatics, and data science applications to research centers and healthcare organizations nationally and abroad. With experts in biomedical science, software engineering, and program management, we focus on developing and applying research tools and techniques to empower decision-making and accelerate research discoveries. We work with some of the top research organizations and facilities in the country including multiple institutes at the National Institutes of Health (NIH). Axle is seeking a Clinical Operations Manager to join our vibrant team at the National Institutes of Health (NIH) supporting the National Institute of Allergy and Infectious Diseases (NIAID) located in Rockville, MD. Benefits We Offer: 100% Medical, Dental & Vision Coverage for Employees Paid Time Off and Paid Holidays 401K match up to 5% Educational Benefits for Career Growth Employee Referral Bonus Flexible Spending Accounts: Healthcare (FSA) Parking Reimbursement Account (PRK) Dependent Care Assistant Program (DCAP) Transportation Reimbursement Account (TRN) Position Information The Clinical Operations Manager provides services and deliverables through the performance of support services for NIAID's Division of Microbiology and Infectious Diseases (DMID). This role requires a Bachelor's degree in a related discipline (or equivalent) and a minimum of seven years of experience in a related field, along with demonstrated experience in program and protocol management and budget tracking, and proficiency with MS Office and SharePoint. Additional Qualifications Certifications & Licenses Bachelor's degree in a related discipline or equivalent. Minimum of seven (7) years of experience in a related field. Field of Study Business Management and Administration Software MS Office SharePoint Skills Demonstrates experience with program and protocol management, and budget tracking. Deliverables Work product and documents related to coordinating with staff to develop a system of standardized procedures for organizing clinical studies/trials logistical functions in accordance with DMID procedures. — Ad-Hoc Work products and documents related to assisting staff for development, collection and quality control of essential clinical studies documents and entry into databases. — Ad-Hoc Work products and documents related to tracking the development of monitoring plans and status of data/safety reviewers. — Ad-Hoc Work products and documents related to coordinating meetings and preparing minutes. — Ad-Hoc Work products and documents related to inventory, organizing, and filing all low resource tiered clinical study documents. — Ad-Hoc Work products and documents related to coordinating 10-day pre-Council application reviews with program staff to ensure they are appropriately assigned. — Ad-Hoc Statement of Work Details Coordinate with RDB and ESTIB ...