HCA, Hospital Corporation of America Data Coordinator in Denver, Colorado
Welcome to theColorado Blood Cancer Institute(CBCI), a part of the Sarah Cannon Cancer Institute at Presbyterian/St. Luke’s Medical Center. Our specially trained hematologists are committed to advancing science and care for patients with blood cancers such as leukemia, lymphoma and myeloma. Having performed more than 4,500 transplants, Colorado Blood Cancer Institute is the largest and most experienced full-service blood and marrow transplant program in Colorado and among the top programs in the country.
CBCI is accredited by the Foundation for Accreditation of Cellular Therapies (FACT), the global standard for top quality patient care in cellular therapies. We work closely with our physician colleagues from New Mexico to Montana to provide patients with nationally recognized care and access to the most innovative clinical trials.
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) . The Data Coordinator provides support to the Clinical Research Coordinator (CRC) and Research Nurse on a daily basis, ensures all activities are conducted according to company standard operating procedures (SOPs) and all applicable Good Clinical Practice (GCP) and ICH regulations and guidelines.
• You will support CRC to meet industry trial data deadlines • You will obtain source documentation for patients enrolled onto clinical trials • You will assist CRC with case report form completion and with query resolution • You will assist in Serious Adverse Event (SAE) reporting and tracking • You will create and maintain patient visit tracking spreadsheets for CTS • You will maintain and archive study administrative files • You will maintain and archive regulatory files • You will assist in ensuring source document templates are accurate. • You will be assigned special procedural projects to enhance the functioning of the research program • Throughout the conduct of the clinical trial you will assess adherence to SCRI SOPS, Good Clinical Practice (GCP) and ICH regulations and guidelines.
What you should have for this role: • Knowledge of scientific, medical, and regulatory terms • Knowledge of GCP and Good Manufacturing Practice (GMP) • Detail-oriented • Excellent English written and oral skills. • Bachelor Degree preferred. • Healthcare experience, Clinical trials support, or pharmaceutical industry experience preferred
Do you want to work on a team fighting together? We are excited to talk with you about this opportunity. Apply now!
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.
Job: *Supervisors Team Leaders & Coordinators
Title: Data Coordinator
Location: Colorado-Denver-Denver Drug Development Unit
Requisition ID: 03058-7249