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Clinical Research Coordinator I | Clinical Coordinator, Clinical Research Coordinator, Research As1

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Clinical Research Coordinator I

Location:
Scottsdale, AZ
Description:

Since 1980, SMIL has evolved into the premier imaging provider in the sout h west. SMIL won the 2016 Southwest Alliance for Excellence award for customer and employee satisfaction, sound management, innovation and results. SMIL was again recognized with the prestigious Advisory Board Company's 2017 Workplace of the Year Award, and in 2019 SMIL was named a World Class Employer by Birdeye Surveys, Inc. Employee engagement is part of everything we do at SMIL. We are dedicated to the growth of our employees including cross training and leadership career opportunities. Simply put, our culture is what sets us apart from the rest. We offer competitive pay, career opportunities and benefits that include; medical, HSA employer contribution, dental, vision, paid time off, paid holidays, 401K and company paid profit sharing, tuition and continuing education reimbursement, paid life insurance, paid long term disability as well as voluntary short term disability. We look forward to having you join our amazing team! Position Summary Under the direction of the Chief Clinical Research Officer, the Clinical Research Coordinator is responsible for conducting clinical trials in accordance with Good Clinical Practice Guidelines, and for contributing to other activities that support the Research Department's operational goals. Responsibilities include Coordinate the execution of research study protocols. Participate in the conduct of clinical research studies conducted by principal investigator(s) including, but not limited to; grant funded research and/or industry sponsored clinical trials conducted onsite at SMIL and offsite at other participating site locations. Under the guidance of a CRC II or manager, overall project management of clinical studies including submission of site feasibility/selection questionnaires, site qualification visits, budget development, procedural training and study implementation. Effective communication of clinical project related information including planning and facilitating of study-related meetings and presentations. Work with community physicians' offices to screen and recruit patients who may qualify for SMIL research studies. Develops flow sheets and other study related documents and completes source documents/case report forms. Comply with protocol guidelines and requirements of regulatory agencies: identify problems and/or inconsistencies and monitor patients' progress to include documentation and reporting of adverse events. Review informed consent forms for accuracy and clarity. Coordinate the day-to-day activities of any technical support staff specifically engaged in the carrying out of research/clinical protocol, as appropriate to the position; may perform aspects of research protocol, as required, in accordance with specified program objectives. Collaborate with physicians and staff to continually improve the clinical research process. Participative in the development of study specific standard operating procedures. Perform other related duties incidental to the work described herein. Qualifications 1-3 years previous experience in a clinical research setting Bachelor's degree in a science or health-related field (or equivalent professional experience) Clinical research certification (ACRP or SoCRA), or scheduled to sit for the exam within next six months (desired) College Accredited Certificate of Completion for Clinical Research Coordinating (helpful) Radiology experience (helpful) Proficient in MS Word, Office, Excel, and ACCESS Experience with phlebotomy and lab processing (desired) Physical Requirements While performing the duties of this Job, the employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms and talk or hear. The employee is frequently required to sit. Specific vision abilities required by this job include close vision, color vision and ability to adjust focus. Job Description Acknowledgement I have received, reviewed and fully understand the job description. I further understand that I am responsible for the satisfactory execution of the essential functions described therein, under any and all conditions as described. Job Posted by ApplicantPro
Company:
Southwest Medical Imaging
Posted:
January 25 on ApplicantList
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More About this Listing: Clinical Research Coordinator I
Clinical Research Coordinator I is a Nurse & Healthcare Clinical Coordinator, Clinical Research Coordinator, Research Associate Job at Southwest Medical Imaging located in Scottsdale AZ. Find other listings like Clinical Research Coordinator I by searching Oodle for Nurse & Healthcare Clinical Coordinator, Clinical Research Coordinator, Research Associate Jobs.