Clinical research studies require production of experimental products, conduct of research studies, laboratory analysis of samples, analysis of resulting data, and submission of study findings.
- The Contractor shall be responsible for the successful execution of clinical trials from startup to closeout, ensuring completion of study deliverables, proactively identify and resolve clinical project issues, and participating in process improvement.
- The Contractor shall manage all clinical aspects of study, including, but not limited to: assessing operational feasibility and recommending study execution plan; developing and managing comprehensive study timelines and metrics; participating in selection and management/oversight of subcontractors; writing and/or reviewing reports, budgets, and metrics; providing study-specific training and leadership to clinical research staff; as well as planning, executing, and leading study-specific meetings.
Required Knowledge, Skills, and Abilities: Preferred knowledge of clinical research procedures; excellent interpersonal and computer skills; ability to communicate effectively and to work with individuals of all levels. The candidate should be well-organized; ability to follow detailed instructions; ability to handle multiple tasks; ability to meet deadlines of projects; ability to facilitate communication among supervisors, team members, and peers.
Minimum Education/Training Requirements: Bachelor's required, Master's Degreepreferred in a related field of study and experience in clinical research or clinical operations positions, progressively leading to clinical project management role.
Minimum Experience: 4-6 years clinical research experience, with at least 2 years in a project management role.
Background Requirement: Eligibility to obtain DoD Common Access Card (CAC) required.