Clinical Research Coordinator

Clinical Research Coordinator#26-01589 $1,950/Weekly Fullerton, CA Allied Health Professional // Clinical Research Coordinator All On-site 13 weeks Job Description Day Shift 8 hours/day 5 days/week

At-a-Glance:

Are you ready to build your career by joining a healthcare provider? If so, our client is hiring a Clinical Research Coordinator.

Position Type:

Contract Onsite Day 5x8-Hour (08:00 - 17:00)

Required:

Must have a minimum of two years of experience in an Oncology specific Clinical Research setting where coordinator managed patients. 5 Years is preferred. Minimum 2 years experience in a clinical research setting where candidate managed patients (consent them, perform vitals/EKG, process labs, dispense medication, complete documentation, enter data)

MUST HAVE EPIC EXPERIENCE

•Must also have strong computer skills - Outlook, MS Teams, Word, Excel Spanish/Korean speaking skills are a plus. Commute is preferred to be 30 minutes or less due to traffic in the area. 4x10 schedule available after 90 day trial period.

Responsibilities:

Oncology Clinical Research Coordinator Under the supervision of the Medical Office Administrator, the Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. This role is responsible for interfacing with the Principal Investigator, Patient, Sponsor, and the IRB. This position is directly responsible to ensure that all documentation is timely and accurate and works closely with the PI to ensure strict compliance to study protocols (GCP/ICH). Reads and understands all correspondence relating to each study assigned. Responsible for all written and verbal communication and the documentation thereof. This will include but not be limited to communications with study sponsors, monitors, study subjects/patients, physicians and laboratories or other study-specified service providers. Responsible for all IP accountability specific to each subject and total protocol inventory. Role includes proper documentation of IP assignment, temperature and expiration date monitoring, return of used IP, and destruction or return to sponsor. Works with subjects/patients to ensure study compliance and understanding of participation requirements (i.e., timeliness of visits, return of study-related materials and at-home documentation. Complete, accurate and timely entry (within 7 days of visit) of visit data into study electronic data capture sites when applicable. Recruits and retains study Participants. Processes, packages, and ships biological samples as required by study or centralized laboratories. Organizes and maintains study binders for each participant in a study. Ensures that filing is complete, accurate and consistent among study participants. Attends investigators' meetings as required. Works with patients to ensure that study requirements are met including appointments, labs, etc. Networks and researches potential new studies. Performs regulatory functions for existing studies. Maintains control over study medications/supplies. Get in

Touch:

We want to hear from you! If you think you'd be a good match, submit your resume and reach out to Lisa at 201-366-0698 to learn more.