Clinical Research Coordinator II or III – Phoenix Vascular Access Office

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Arizona Kidney Disease and Hypertension Center (AKDHC) is one of the nation’s largest groups of physicians specializing in the care of patients with renal disease. Since 1976, we have enjoyed the trust of patients and the respect of the community throughout the Phoenix Metropolitan area and across Arizona. We are a professional medical association consisting of physicians and other vital support staff.

We are seeking a Clinical Research Coordinator II or III to join our team. To learn more about us, please visit our website:  .

Clinical Research Coordinator II or III – AKDHC Phoenix Vascular Access Office

With the support of the Clinical Research Operations Manager, the Clinical Research Coordinator II or III will provide research study assistance and coordination services to different clinical research areas for AKDHC Medical Research Services, LLC. You will also be responsible for assisting the Principal Investigator and ancillary staff in educating patients about research studies. Clinical Research will include clinical trials in our regular nephrology offices, as well as our surgery center and dialysis units.

• Promotes research studies’ initiation and review, including completion of associated reports/questionnaires.
• Promotes the positive growth of research within the company
• Supports other team members with Research related activities
• Represents AKDHC Medical Research Services, LLC and/or NKDHC, LLC at Investigator meetings as needed (requires out of state travel)
• Complies with Standard Operating Procedures in all research activities
• Applies knowledge of FDA CFR Regulations and ICH Guidelines to all research activities
• Coordinates multiple clinical trials in various stages of development
• Routinely and consistently travels between multiple sites to conduct patient visits, meet with sponsor representatives, and conduct in-services as necessary
• Required to perform as stand-in/back-up to other team members as needed and under the guidance of the Primary Coordinator of the respective study
• Maintains working knowledge of all currently enrolling studies and assists as back-up to other team members as needed
• Maintains a thorough working knowledge through studying to achieve Clinical Research Coordinator Certification (if not already attained) and assists in the training and continued support of new Clinical Research Coordinator (if already attained)
• Maintain the ability to provide basic patient care including: the use of medical terminology, understanding basic lab values, vital sign assessment, phlebotomy, medication administration under the direction of the PI, the ability to recognize adverse events and/or patients in distress requiring advanced patient care and reporting the same to the appropriate personnel
• Assists in routine internal audits and in-house monitoring to ensure high quality research and adherence to protocol
• Perform other tasks as assigned by the Clinical Research Operations Manager
• Maintain a positive, pleasant, professional working relationship with all research and ancillary staff.

• Bachelor’s degree in Nursing or a related field, Clinical Research Coordinator Certification (for III) and/or comparative work experience
• Certificates and Licenses:
  Clinical Research EDC, GCP, and IATA training certificates; knowledge of ICH guidelines, GCP, and the clinical trial study process
• At least 3-5 years’ experience in Clinical Research
• Experience in coordinating all aspects of clinical research trials
• Ability to train other Clinical Research Coordinator and to act as Lead Coordinator (for III)
• Demonstrated application of medical knowledge and ability to understand and comply with protocol demands
• Excellent communication skills (both written and verbal)
• Detail oriented and problem solving ability
• Excellent patient care skills
• Ability to work with a team and handle multiple projects
• Excellent organizational, data management, and…