Reporting to the Contracts Manager and under general direction, the Senior Contracts Specialist will provide technical and administrative contracts support to scientific and administrative staff in support of the Institute's mission.
The Senior Contracts Specialist will provide end-to-end execution of Federal and commercial contracts by ensuring compliance with Institute policies, Federal regulations affecting grants, competitive contracts and/or solicitations, and the terms of commercial contracts. Will review and ensure accuracy of pricing data of budgets, review contractual documents and agreements, make recommendations about best practices for contract compliance, and assist the Contracts Manager with all other related contractual administration duties and tasks as required or assigned.
Will also generate and complete pre and post award documents including but not limited to, Service Agreements, Work, Delivery and Task Orders, Amendments and shall conduct customer contract reviews as necessary.
Will work in a fast paced, team-oriented environment and will provide general direction and support to junior specialists, and may assist with oversight of the Office of Research Contracts (ORC) in the absence of the Contracts Manager.
Requires a bachelor's degree in Business Administration/Accounting, Public, or related field and 4+ years of directly related professional-level contract administration experience; or an equivalent combination of education, training and/or experience from which comparable knowledge, skills and abilities have been attained.
The Senior Contracts Specialist must have demonstrated experience working in a commercial or Federal contracting environment and a fundamental understanding of standard best practices surrounding contractual agreements. Must be able to perform basic mathematical calculations on budget and proposal reviews in Excel and other similar software products and have the ability to independently explain financial data to management and scientific personnel as needed.
This position requires a fundamental understanding of and previous experience applying contractual regulations including, but not limited to, FAR, DFARS and Federal cost principles contained in 2 CFR 200. Basic knowledge of and experience with the Institute's major funding agencies—NIH, DOD, NSF, DHS—is strongly preferred.
Must have superior professional-level written and verbal communication skills; a high degree of professionalism, excellent judgment, problem-solving and decision-making skills. Demonstrated ability in managing a wide variety of complex tasks and projects simultaneously while meeting multiple deadlines is required. Must have the ability to work independently or as a part of a team and have computer proficiency with Microsoft Office and the ability to learn department-specific computer systems as needed.
Experience with Pro-Pricer or other similar budgeting databases as well as experience in a research environment and knowledge of government acquisitions is strongly preferred.
This position requires a post-offer credit check.
Work is performed in an office environment. Will operate standard office equipment and will frequently stand, walk, sit, perform desk-based computer tasks, use a telephone, perform repetitive motions and occasionally lift objects that weigh up to 10 pounds. The above is intended to describe the general requirements for the position and should not be interpreted as an exhaustive statement of physical requirements. The Institute will provide reasonable accommodation to any employee with a disability who requires an accommodation to perform the essential functions of the position.
Salary is commensurate with experience.
Lovelace Biomedical is an Equal Opportunity Employer
Building on a history of pioneering science and technological innovation, Lovelace Biomedical is a contract research organization that helps pharmaceutical and biotechnology companies advance their discoveries—no matter how complex—into clinical testing and beyond. The organization leverages a multidisciplinary toolset to push the limits of preclinical research and fully understand the behavior of its clients’ investigational products. Lovelace Biomedical provides a unique experimental breadth and logistical capacity to solve specialized challenges that other CROs are not equipped to handle, featuring expansive bio-secure facilities and ongoing access to industry-leading scientific experts. The team thrives on developing programs for complex diseases, emerging drug classes and delivery mechanisms, and challenging areas of drug development while delivering the same level of rigor and attention to seemingly straightforward studies that are just as critical to regulatory success.
