Clinical Research Assistant

Balboa Care Nephrology Research Enterprise United • Chula Vista, CA

23d • Onsite

About The Position

The Research Assistant will provide the Clinical Research Coordinator with direct clinical and administrative data management assistance regarding the collection and reporting of delegated trials. With the ability for high level thinking and attention to detail, the Research Assistant will cross-check, create, record, report, and distribute study related information for regular review by the Clinical Research Coordinator.

Requirements

• A High School diploma and one year of experience, preferably in clinical research, human medicine, end stage disease or an equivalent combination of education and experience; knowledge and abilities relevant to the successful conduct of the Research Assistant position.
• Valid driver’s license and dependable transportation to travel locally between sites.
• Experience with study protocols and a record of successful collection, recording, and reporting of data with written and online databases.
• Exhibits the capacity to work unattended and complete delegated tasks by specified dates.
• Demonstrates experience to independently review data for completeness and quality assurance related to the collection and reporting of clinical data.
• Experience in HIPAA and GCP/ICH including federal and local record management.
• Regularly required to talk, hear, read, write, type and respond in English and understand clinical/medical vocabulary written and spoken.
• Vision requirements include close vision, ability to adjust focus, and see color.

Nice To Haves

• Experience in CKD, Dialysis or Renal transplantation.
• Experience working in EDC, CTMS and EMR systems.
• Skilled in lab techniques, processing, and shipping of human biologics.
• Established experience in medical terminology.
• Bilingual in English and Spanish

Responsibilities

• Timely EDC, CTMS, and other study related vendor portal data entry.
• Cross-checking for accuracy of all data in online portals or vendors.
• Subject visit tracking and scheduling per protocol.
• CRO and Sponsor related scheduling & correspondence support for the Clinical Research Coordinator.
• Assist in source creation, recording, reporting, and cataloging.
• Aids in maintaining federal and GCP/ICH compliance during the conduct of trials.
• Perform, record, and report delegated study visit tasks per protocol ie; subject intake, EKG’s and trial specific biologic sample collection.
• Collect, process, and ship trial specific biologic samples per protocol.
• Manage and maintain trial related supply inventory.

Benefits

• Medical, dental & vision on the 1st of the month 30 days after hire.
• Employer contribution of up to 7.5% of annual pay for your 401K.
• Generous paid time off plus 8 paid holidays, a birthday float day off and a mental health day!
• Company paid life insurance.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED