Quality Assurance Consultant in Nashville, Tennessee, United States
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Sarah Cannon Network

Quality Assurance Consultant

Nashville, TN, United States
Full-time • Days 7-10 Hrs/Wkdays Only
Case Management   Job ID: 4131
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Sarah Cannon Development Innovations is a full-service contract research organization (CRO) that is uniquely focused in oncology. Sarah Cannon Innovations offers strong scientific leadership, access to patients through Sarah Cannon Research Institute’s Site Management Organization (SMO) and relationships with other clinical sites, and experience in drug development and delivery of clinical trials from First-In-Man through registration level studies, making us the partner of choice for oncology.

Sarah Cannon, the global cancer enterprise of Hospital Corporation of America (HCA), offers integrated cancer services with convenient access to cutting-edge therapies for those facing cancer in communities across the United States and United Kingdom.

Are you passionate about delivering superior, patient-centered care? At Sarah Cannon, we are committed to caring for patients with purpose and integrity. We care like family! Jump-start your career as a Quality Assurance Consultant today with Sarah Cannon.

As the Quality Assurance Consultant, you are responsible for implementing the quality assurance program, managing and performing consult visits at investigative sites, assisting with onsite external audits and inspections, and providing routine quality support for assigned investigative sites.

Duties include but are not limited to:

  • You will perform process/focused audits (as needed) of research sites utilizing research audit tools to ensure quality and reports audit findings to the appropriate leadership.
  • You will monitor and modify policies and procedures for the investigative sites, utilizing quality tools that assess the quality indicators of study operations
  • You will identify areas of deficiency in quality and report those deficiencies to SC Directors and other appropriate colleagues
  • You will assist the investigative sites in development and modification of clinical research SOPs and Work Instructions
  • You will assist with preparation and hosting of external audits and assist research staff in maintaining FDA compliance, while assisting sites with responses to external audits and CAPA development.
  • You will communicate observations and deficiencies to the Site Director / Manager and study PI, as appropriate.


For this position, you must have:

  • Bachelor's Degree (4 yr. program)
  • At least 3 years’ experience in a CRO/Sponsor environment/Biotech and/or quality department
  • Experience in a GCP environment

Be a part of an organization that invests in you. We are actively reviewing applications for our Quality Assurance Consultant opening. Highly qualified candidates will be promptly contacted for interviews. Submit your application and help us raise the bar in patient care!

We offer you an excellent total compensation package, including competitive salary, excellent benefit package and growth opportunities. We believe in our team and your ability to do excellent work with us. Your benefits include 401k, PTO medical, dental, flex spending, life, disability, tuition reimbursement, employee discount program, employee stock purchase program and student loan repayment. We would love to talk to you about this fantastic opportunity!

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.


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Case Management
Full-time • Days 7-10 Hrs/Wkdays Only

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