Kelly · 15 hours ago
Clinical Trials Technology Transfer & Agreements Manager
Kelly Government Solutions is a strategic supplier and business partner to the federal government, seeking a Clinical Trials Technology Transfer & Agreements Manager to support the National Institutes of Health (NIH). The role involves drafting and negotiating various agreements, providing project management support, and ensuring compliance with NCI/NIH policies.
Responsibilities
Provide support for the drafting and negotiation of Cooperative Research and Developments Agreements for NCI scientists and their industrial/academic research partners
Provide support for the planning and negotiation of Material Transfer Agreements (MTAs), Clinical Trial Agreements (CTAs) and other technology transfer agreements
Liaise with MATCH stakeholders, both internal and external
Provide support to staff in ensuring that agreements in the MATCH program are consistent with existing agreement and NCI/NIH policy
Provide agreement support and coordination between CDP and CTEP
Create data/monitoring plans and provides regular written reports detailing progress against tasks and milestones
As the NCI Formulary CRADA negotiations. Maintain the “Active Agreements” list on the CTEP Website of current CTEP Agents available for request
Collaborate with NCI and other stakeholders to implement key process improvement initiatives
Maintain the ACG SharePoint Page as requested. Provide scientific and administrative project management support
Develop a new tracking and reporting system for the Biomarkers and Medical tests funding sources. 2 Generate appropriate SOPs and workflows for the new processes
Monitor project risk by proactively anticipating issues and develops contingency plansand solutions. Work with the CTEP to immediately address issues as they arise
Monitor LOIs and protocols to make an early determination of associated correlative work funding mechanism (CRADA, MoCha, NCLN, grants, etc.)
Collaborate with CTEP IDB, CDP and RAB staff to ensure associated correlative work is identified
Collaborate with internal and external stakeholders for intellectual property requirements, CRADAs, MTAs, etc. 5 Work with CTEP and contracting project management staff to ensure the operational needs of the project are being met
Coordinate with NCI, CRADA partners and CTEP to track timeline and pending financial support
Qualification
Required
Master's degree in Biological Sciences or Life Sciences
Minimum of three (3) years of experience
Clinical trial project management experience
Ability to problem solve and prioritize assignments/tasks
Ability to do work assignments and/or projects successfully and completed in a timely manner
Familiarity with area of clinical trials preferably in the field of Oncology
Previous project management experience and/or clinical trial management including data management
Familiarity with research subcontracting
Exceptional written and oral communication skills
Ability to work in a busy setting, both independently and within a team
Ability to communicate effectively with high-level personnel
Ability to attend meetings as a program liaison
Willingness to perform tasks that may fall outside of the normal daily responsibilities
Ability to obtain and maintain a security clearance
Benefits
Competitive compensation and comprehensive benefit package
Optional health, vision, and dental plans
Vacation leave as well as 10 paid federal holidays and 401K plan.
Company
Kelly
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Funding
Current Stage
Public CompanyTotal Funding
unknown1978-01-13IPO
Leadership Team
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Kelly Services, Inc.
2025-11-08
2025-11-08
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