Manager of Early Phase Operations at HCA
Nashville, TN
About the Job
Description
Standard
Qualifications:
Standard
Qualifications:
Sarah Cannon is theresearch arm of HCA’s global cancer enterprise. Focused on advancing therapiesfor patients, it is one of the world’s leading clinical research organizationsconducting community-based clinical trials in oncology, cardiology andorthopedics through affiliations with a network of more than 1,000 physiciansacross the United States and United Kingdom.
We believe our success is dependent on a healthywork environment where staff members are the core of advancing therapies forpatients and accelerating drug development. We apply the same compassion andcommitment we have for our patients to our co-workers and colleagues andpromote an entrepreneurial culture.
Benefits:
- Tuition Reimbursement/Assistance Programs
- Paid Personal Leave
- 401k (100% annual match – 3%-9% of pay based on years of service)
- Identity Theft Protection discounts
- Auto, Home, and Life Insurance options
- Adoption Assistance
- Employee Stock Purchase Program (ESPP)
As the Manager of Early Phase Strategic Sites Operations you are responsible for establishing effective relationships with leadership and colleagues at Sarah Cannon and assigned Strategic Sites.
- You are responsible for collaborative support and oversight of assigned Oncology Sites to achieve site goals, financial and quality performance, and facilitate patient access to applicable clinical trials. You will be responsible for individual site goals, financial performance, quality assurance, oversight and patient enrollment
- You will communicate to all stakeholders performance standards and expectations
- You will be responsible for collaborative oversight of research site operations
- You will assist with continuing education and training to investigators and research Staff
- You will create and support strategic and tactical plans for site growth
- You will coordinate and assist with the process of on-boarding and training new research sites
- You will assess available research resources and facilitate those resources within each site
- You will problem solve clinical situations as they arise, collaborating with research program members as needed
- You will assess and ensure compliance with Quality and Regulatory department members
- You will assist in development and tracking of quarterly goals for each site
- You will work closely with site, sponsor/CRO monitors, and study managers to quantify the quality and timeliness of study data
- You will assist with assuring ongoing research conduct at sites as needed
- You will meet with physicians and administrators as needed to assess performance of site
- You will monitor patient enrollment at sites through weekly reports
- You will facilitate communication of site status to appropriate site/management colleagues
- You will represent the company vision to sites colleagues and affiliated organizations
- You will travel to Oncology Strategic Sites as determined by leadership and need