HCA, Hospital Corporation of America Clinical Research Coordinator in Denver, Colorado
Welcome to theColorado Blood Cancer Institute(CBCI) , a part of theSarah Cannonat 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 3,000 transplants, CBCI is the largest and most experienced full-service blood and marrow (stem cell) transplant program in Colorado and among the top programs in the country. We are 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: 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.
* * * Summary of Key Responsibilities:The Clinical Research Coordinator, Blood Cancer/BMT is responsible for overall clinical operations of the facility’s blood cancer research program including enrollment, regulatory, quality, and site operations. * * *Duties and Responsibilities: Duties include but are not limited to: * Supports enrolling patients onto clinical trials through recruitment, screening, enrollment, treatment, and follow-up of eligible participants according to protocol requirements. * Reviews the study design and inclusion/exclusion criteria with physician and patient * Ensures the protection of study patients by verifying informed consent procedures and adhering to protocol requirements * Collects, completes, and enters data into study specific case report forms (CRFs) or electronic data capture systems within study required timelines * Ensures the integrity of the data submitted on case report forms or other data collection tools by careful source document review; monitors data for missing or implausible data * Ensures that adequate and accurate records are maintained for inspecting * Creates study specific tools for source documentation when not provided by sponsor * Generates and tracks drug shipments, lab kits, and other supplies as needed * Reports and follows up on serious adverse events as per the protocol and regulations * Implements study-specific communications * Responsible for accurate and complete documentation of protocol requirements according to site work instructions/SOPs * Tracks and reports adverse events, serious adverse events, protocol waivers, and deviations * Communicates all protocol-related issues to appropriate study colleagues and stakeholders * Maintains accurate and complete records, including regulatory documents, signed informed consent forms, source documentation, drug dispensing logs, screening and enrollment logs, and study communications * Coordinates regular site research meetings * Attends study-specific on-site meetings/visits, investigator meetings, conference calls, and other coordinator meetings, as required. * Ensure GCP, SOP, and protocol training and compliance of all team members * Problem solves clinical situations along with research staff as they arise * Assists in tracking of and reporting of quarterly goals for research program * Works closely with monitors, study teams and site staff to ensure quality study data * Supports strategic and tactical plans for site growth * Communicates site status through a weekly activity report to appropriate site/management colleagues * Represents the company vision to site colleagues and affiliated organizations
Knowledge: * Medical and research terminology * FDA Code of Federal Regulations and GCP * Sarah Cannon organizational policies, standard operating procedures and systems * Clinical research processes Skills: * Verbal and written communication skills * Analytical, problem-solving, and multi-tasking skills * Organizational skills * Computer skills * Public presentation skills
Abilities: * Interpersonal skills * Work independently in a fast-paced environment with minimal supervision at off-site facilities * Manage multiple ongoing priorities and projects * Communicate and work effectively with a diverse team of professionals
Education: Associate Degree Required Bachelor Degree Preferred
Experience: * At least one year of oncology experience, preferably heme/onc and/or transplant * At least one year of experience in a clinical research setting * At least one year of experience managing blood cancer and/or BMT clinical trials preferred * * Certification or License: Research certification (ACRP or CCRP) RN or LPN preferred
Do you want to be a part of a team working together to fight cancer? * * We are so excited to speak with you about this phenomenal opportunity. Apply to hear more.
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: Clinical Research Coordinator
Location: Colorado-Denver-Denver Drug Development Unit
Requisition ID: 03058-6270