Clinical Research Coordinator

RadNet • Anaheim, CA

23d • Onsite

About The Position

Artificial 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.

Requirements

• 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
• Genuinely passionate about customer service and exercise sound judgement and an ability to remain professional in all situations
• Able to demonstrate high level of attention to detail, excellent organizational skills and have the ability to multitask
• Able to thrive in a fast-paced environment, have a knack for prioritizing work with a structured approach, and enjoy providing world class customer service

Nice To Haves

• Bachelor's degree or higher may substitute for experience

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

Benefits

• Comprehensive Medical, Dental and Vision coverages.
• Health Savings Accounts with employer funding.
• Wellness dollars
• 401(k) Employer Match
• Free services at any of our imaging centers for you and your immediate family.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED
• Number of Employees: 5,001-10,000 employees