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Hospital Corporation Of America (HCA) Data Coordinator in Denver, Colorado

DESCRIPTION SHIFT: No WeekendsSCHEDULE: Full-timeWelcome to the COLORADO BLOOD CANCER INSTITUTE (CBCI), a part of theSarah Cannon Cancer Institute at Presbyterian/St. Luke's Medical Center.Our specially trained hematologists are committed to advancing science andcare for patients with blood cancers such as leukemia, lymphoma and myeloma.Having performed more than 4,500 transplants, Colorado Blood CancerInstitute is the largest and most experienced full-service blood and marrowtransplant 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 cellulartherapies. We work closely with our physician colleagues from New Mexico toMontana to provide patients with nationally recognized care and access to themost 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 ResearchCoordinator (CRC) and Research Nurse on a daily basis, ensures allactivities are conducted according to company standard operating procedures(SOPs) and all applicable Good Clinical Practice (GCP) and ICHregulations and guidelines.* You will support CRC to meet industry trial data deadlines* You will obtain source documentation for patients enrolled onto clinicaltrials* You will assist CRC with case report form completion and with queryresolution* 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 functioningof the research program* Throughout the conduct of the clinical trial you will assess adherence toSCRI SOPS, Good Clinical Practice (GCP) and ICH regulations and guidelines. QUALIFICATIONS 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 pharmaceuticalindustry experience preferred DO YOU WANT TO WORK ON A TEAM FIGHTING TOGETHER? WE ARE EXCITED TOTALK WITH YOU ABOUT THIS OPPORTUNITY. APPLY NOW!We are an equal opportunity employer and value diversity at our company. We donot discriminate on the basis of race, religion, color, nationalorigin, gender, sexual orientation, age, marital status, veteranstatus, or disability status. NOTICE Our Company's recruiters are here to help unlock the next possibilitywithin your career and we take your candidate experience very seriously.During the recruitment process, no recruiter or employee will requestfinancial or personal information (Social Security Number, credit card orbank information, etc.) from you via email. The recruiters will not emailyou from a public webmail client like Gmail or Yahoo Mail. If you feelsuspicious of a job posting or job-related email, let us know by clickinghere. For questions about your job application or this site please contactHCAhrAnswers at 1-844-422-5627 option 1.Employer's Job# 03058-7249Please visit job URL for more information about this opening and to view EOEstatement.

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