We are looking for a well experienced CRC to support a large organization within their phase I unit. The ideal candidate will have Oncology experience and 2 years of experience as a CRC. This position is 100% onsite!

Description:

Clinical Research Coordinators (CRC) perform protocol specific duties relevant to the clinical trial.

Scope of Support:

• Administrative Support customized site level support, such as support with regulatory document submissions and perform chart reviews/EMR interrogation
• Prescreening including review of concomitant meds, medical history, and inclusion/exclusion criteria to identify potential patients
• Scheduling Visits including appointment reminders
• Data Entry and Query Resolution based on data available in source documents and ensure data entry and responses are completed within protocol designated windows
• External Referral Outreach including grassroots effort to distribute study recruitment materials in and around sites, community outreach
• Contact, prescreen, and schedule referrals from outreach campaign
• Conduct Study Visits
• Perform ICF process following GCP
• Identify and enroll qualified participants for ongoing and new clinical trials, through collaboration with PIs, use of study portals, and other tools.
• Oversees data and ensures that it is being entered correctly and resolves any queries issued within required time frame
• Collects and reports ALL Adverse Events
• Collects and reports ALL Serious Adverse Events