- 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
- Passionate about patient care and exercise sound judgement and an ability to remain professional in all situations.
- You demonstrate effective and professional communication, interpersonal skills and respect with patients, guests & colleagues.
- You have a structured work-approach, understand complex problems and you are able to prioritize work in a fast-paced environment.
- High school graduate (some college preferred)
- MA certificate, or at least 2 years in a clinical setting or imaging center
- At least 2 years in a research environment with study operations responsibilities
- Bachelor's degree or higher may substitute for experience
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Research Coordinator - Thousand Oaks, United States - RadNet
Description
ResponsibilitiesArtificial Intelligence; Advanced Technology; The very best in patient care. With decades of expertise, we are Radiology Forward.
With dynamic cross-training and advancement opportunities in a team-focused environment, the core of our success is its people with the commitment to a better healthcare experience.
When you join us as a Clinical Research Coordinator you will be joining a dedicated team of professionals who deliver quality, value, and access in the 21st century and align all stakeholders- patients, providers, payors, and regulators to achieve the best clinical outcomes.
You Will:
If You Are: