Clinical Research Coordinator

Responsibilities

The Clinical Research Coordinator will be responsible for all aspects of imaging clinical trials within our Research Department. This position has a Monday

• Friday 8:00am

• 4:30pm schedule and will report out of our office in Anaheim, CA.

The CRC will assist with facilitating training and document training, ensure adherence to GCP standard and Human Subjects Protection standards. The CRC will ensure delegation logs and study binders contain complete and up to date records. The CRC will assist the lead Research Assistant in any duties that pertain to the study start up process. They will work closely with the regulatory coordinator with any documentation requirements. This position will interact with Sponsors, Study groups, CRO's, and all RadNet imaging departments who participate in the conduct of research to meet contractual obligations.

Essential Duties and Responsibilities

• Works with broad spectrum of health care providers for many disease types, physicians, nurses, other research coordinators, imaging techs and support staff

• Read and interpret research study protocols in order to define the procedures that will be provided to the clinical research site

• Translate the designated study procedures into a plan for operational implementation

• Must be able to articulate study process and produce study flow and source documents that are instructive to the technical and clerical staff

• Maintain impeccable records of all interactions with clients and companies

• Assures confidentiality of patient's records and study related materials that are provided under non-disclosure agreements by the research site, pharmaceutical company, or imaging vendor

• Assist the scheduling team with any problems or difficulties to achieve patient study time lines

• Maintains accurate study files

• Provides each imaging site with binders and assists them with relevant information in order to procure correct imaging for each study

• Visits multiple imaging centers in California to ensure training and study compliance.

• Attends on site pre study and site initiation visits as needed

• Adjusts schedule to ensure site visits and training sessions can be accomplished

• Must be able to problem solve and resolve data queries in a timely manner

• Work environment is organized and functions efficiently

Requirements:

• High school graduate (some college preferred)

• MA certificate, or at least 2 years in a clinical setting or imaging center

• At least 1 year in a research environment with study operations responsibilities-Preferred

• Bachelor's degree or higher may substitute for experience

This position often requires sitting, standing, walking, bending, twisting reaching with hands and arms, using hands and fingers, handling, constant talking, and hearing. Visual acuity to read computer screens and written materials. Also, must be able to lift over 20 pounds, occasionally.

Representatives work in a medical office or setting with low to moderate noise level.

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