Clinical Research Coordinator II-258902
Medix™ · Denver, Colorado, United States
FULL TIMEpermanent
Job Description
We are seeking a highly adaptable Clinical Research Coordinator (CRC) based in Longmont, CO, Littleton, CO, or Midtown, CO to support trial operations across a site network. Working alongside site leadership and internal departments, you will drive patient screening, care coordination, and regulatory compliance to ensure the successful execution of complex, patient-centered oncology studies.
Increase your chances of an interview by reading the following overview of this role before making an application.
ResponsibilitiesScreen patients post-physician visit (in-person or via phone) to determine eligibility for a doctor's specific trial or across all site studies. Conduct thorough patient education and informed consent processes.Balance a dynamic workload (approximately 60% administrative / 40% patient-facing), managing an active load of ~20 patients (varying from 2 to 10 per week) and navigating up to 90 active site studies.Partner with internal departments—including Imaging, Labs, and Radiology—to seamlessly align protocol-required procedures and ensure high-quality patient care.Administer oral Investigational Product (IP) to trial participants and meticulously handle the accountability and return shipping of IP back to the central hub.Complete accurate clinical data entry and diligently maintain regulatory documentation to ensure ongoing trial compliance and audit readiness.Required Skills3 to 5 years of clinical research experience with some direct experience supporting oncology trials. Prior hands-on experience navigating complex trial workflows, protocol administration, and adverse event tracking.Proven ability to pivot quickly when unscheduled tasks arise, such as setting aside administrative computer work to conduct immediate patient screenings.Demonstrated capability in independently consenting patients, managing oral Investigational Product (IP) accountability/disbursement, and preparing for sponsor or CRO monitoring visits. xzbcwsv Ability to work a full-time, Monday through Friday schedule on-site.
Increase your chances of an interview by reading the following overview of this role before making an application.
ResponsibilitiesScreen patients post-physician visit (in-person or via phone) to determine eligibility for a doctor's specific trial or across all site studies. Conduct thorough patient education and informed consent processes.Balance a dynamic workload (approximately 60% administrative / 40% patient-facing), managing an active load of ~20 patients (varying from 2 to 10 per week) and navigating up to 90 active site studies.Partner with internal departments—including Imaging, Labs, and Radiology—to seamlessly align protocol-required procedures and ensure high-quality patient care.Administer oral Investigational Product (IP) to trial participants and meticulously handle the accountability and return shipping of IP back to the central hub.Complete accurate clinical data entry and diligently maintain regulatory documentation to ensure ongoing trial compliance and audit readiness.Required Skills3 to 5 years of clinical research experience with some direct experience supporting oncology trials. Prior hands-on experience navigating complex trial workflows, protocol administration, and adverse event tracking.Proven ability to pivot quickly when unscheduled tasks arise, such as setting aside administrative computer work to conduct immediate patient screenings.Demonstrated capability in independently consenting patients, managing oral Investigational Product (IP) accountability/disbursement, and preparing for sponsor or CRO monitoring visits. xzbcwsv Ability to work a full-time, Monday through Friday schedule on-site.
Details
| Company | Medix™ |
| Location | Denver, Colorado, United States |
| Type | FULL TIME |
| Niche | hr |
| Experience | permanent |