Clinical Research Coordinator - Oncology

About the role

The primary responsibilities of a Clinical Research Coordinator (CRC) are; patent accrual, data management, protocol administration, and patient education. Patient accrual encompasses identifying eligible patients for LMHS IRC approved Clinical Trials. Data Management encompasses the on-study and long-term data management of every patient entered into a LMHS Clinical Trial. Protocol Administration encompasses maintaining protocol compliance with cooperative groups and adhering to the LMHS IRC guidelines. The last component is patient education. The CRC is responsible for educating the patient, staff and physicians on LMHS IRC approved Clinical Trials.

Requirements

• Education: Degree/Diploma ObtainedProgram of StudyRequired/ Preferredand/or Bachelor'sPreferred
• Experience: Minimum Years RequiredArea of ExperienceRequired/ Preferredand/or 1 YearClinical trials data managementRequired

Additional Requirements

• Licenses: LicensesRequired/ Preferredand/or
• Certifications/Registrations: Certificates/RegistrationsRequired/ Preferredand/or

Good communication skills, good computer skills, including word, Excel and navigating the Internet. Good customer service skills are required.

Pay

$21.54 - $26.93 / hour

Schedule

Shift 1/8:00:00AM to 4:30:00PM