Job Description

Description

SHIFT: No Weekends
SCHEDULE: Full-time
Salary Estimate: $56929.60 - $79622.40 / year
Learn more about the benefits offered for this job.

The estimate displayed represents the typical salary range of candidates hired. Factors that may be used to determine your actual salary may include your specific skills, how many years of experience you have and comparison to other employees already in this role. The typical candidate is hired below midpoint of the range.

Welcome to the Colorado Blood Cancer Institute (CBCI) , a part of the Sarah Cannon at Presbyterian/St. Lukes 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:

* * Student Loan Repayment
* 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 Clinical Research Coordinator for Blood Cancer and Bone Marrow Transplant (BMT) research you are responsible for overall clinical operations of the facilitys blood cancer research program including enrollment, regulatory, quality, and site operations.

* You will support enrolling patients onto clinical trials through recruitment, screening, enrollment, treatment, and follow-up of eligible participants according to protocol requirements.
* You will reviews the study design and inclusion/exclusion criteria with physicians and patients
* You will ensure the protection of study patients by verifying informed consent procedures and adhering to protocol requirements
* You will collect, complete, and enter data into study specific case report forms (CRFs) or electronic data capture systems within study required timelines
* You will ensure the integrity of the data submitted on case report forms or other data collection tools by careful source document review and monitoring data for missing or implausible data
* You will create study specific tools for source documentation when not provided by sponsor
* You will generate and track drug shipments, lab kits, and other supplies
* You are responsible for accurate and complete documentation of protocol requirements according to site work instructions and standard operating procedures (SOPs)
* You will track and report adverse events, serious adverse events, protocol waivers, and deviations
* You will maintain accurate and complete records, including regulatory documents, signed informed consent forms, source documentation, drug dispensing logs, screening and enrollment logs, and study communications
* You will coordinate regular site research meetings
* You will attend study-specific on-site meetings/visits, investigator meetings, conference calls, and other coordinator meetings, as required and you will work closely with monitors, study teams and site staff to ensure quality study data
* You will communicate site status through a weekly activity report to appropriate site/management colleagues

Qualifications

You should have for this position:

* An Associates Degree, preferably a Bachelors Degree
* Knowledge of medical and research terminology
* Knowledge of FDA Code of Federal Regulations and GCP
* Knowledge of the clinical research processes
* Public presentation skills
* The ability to manage multiple ongoing priorities and projects with a diverse team of professionals
* At least one year of oncology experience, preferably in hematology/oncology 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 is preferred
* Research certification (ACRP or CCRP) is preferred
* RN or LPN is 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.

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