Project Manager III - NCCT Study Oversight Manager
About The Position
The National Center for Clinical Trials (NCCT) is designed to serve as an innovative platform to revolutionize and catalyze the conduct of clinical trials−greatly accelerating the translation of scientific findings into improvements in the prevention, diagnosis, and treatment of disease for our communities and patients. The NCCT will offer core services for patient recruitment and enrollment, trial administration and follow-up, and to gather real world data and evidence. This position will be part of a team that will report to leadership in the NCCTand will manage the clinical trial feasibility review process and the oversight of trial performance.
Requirements
- Master's degree related to project management and evaluation, such as Epidemiology, Public Health, Psychology, or Sociology and four years of relevant administrative and medical experience in research projects or other health-related activities; or, an equivalent combination of education and experience.
- Two years' experience in a supervisory capacity.
- Must have 4+ years managing projects and/or processes.
- Must have 2 years in a supervisory capacity.
- Must have 5+ years of experience working with clinical trials.
- Working knowledge of clinical trial management systems and electronic medical records.
- Detailed understanding of clinical trial operations and challenges from the site perspective.
- Experience in leading teams and in decision-making role(s).
- Excellent written and verbal communication skills.
- Excellent organizational skills and attention to detail.
- Demonstrated ability to work independently as well as in a team environment.
- Proficiency with Microsoft Office, Microsoft Excel and Microsoft PowerPoint.
Responsibilities
- Study Oversight Manager monitors and manages the overall progress of the trial.
- Facilitates and attends site initiation visits.
- Responsible for outreach to applicable physicians, care teams, etc. to gain valuable information.
- Maintain working knowledge of clinical trials within research portfolio.
- Connects study staff members with training resources as necessary for compliance with policies.
- Monitors progress of the clinical trial until completion ensuring accrual, study activities and quality measures are met.
- Liaises with regulatory to monitor amendments, personnel changes, etc.
- Liaises with sponsor, investigator(s) and site staff throughout trial.
- Monitors resource demands throughout trial.
- Supports the deployment of coordinators and Advanced Care Providers to sites as needed for study conduct.
- Performs other related duties incidental to the work described herein.
Benefits
- Paid Time Off programs
- Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
- Flexible Spending Accounts for eligible health care and dependent care expenses
- Family benefits such as adoption assistance and paid parental leave
- Defined contribution retirement plans with employer match and other financial wellness programs
- Educational Assistance Program
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What This Job Offers
Job Type
Full-time
Career Level
Manager
