Clinical Research Diabetes Specialist (Registered Dietitian or Registered Dietitian Nutritionist) - PRN/ Contract

Wake Research•Chattanooga, TN

11d•Onsite

About The Position

M3 Wake Research, an M3USA Company, is seeking a Clinical Research Diabetes Specialist for a PRN contract position. This role is primarily responsible for providing specialized care to people living with diabetes through onsite and virtual visits, adhering to research protocols and ensuring the health, safety, and welfare of participants. The specialist will also be involved in nutrition education and counseling for individuals with diabetes and play a significant role in the conduct of research studies.

Requirements

Registered Dietitian or Registered Dietitian Nutritionist.
Minimum of 2 years of experience of relevant work experience.
Graduate from an accredited school with a degree in nursing, dietetics, food and nutrition, or related program.
Registered Dietitian (RD) or Registered Dietitian Nutritionist (RDN) Certification.
Current and unrestricted State License (RD/RDN) in good standing (as applicable). TN license required.
Certified Diabetes Care and Education Specialist (CDCES) or Certified Diabetes Educator (CDE) from the Certification Board for Diabetes Care and Education (CBDCE) or equivalent combination of education and experience.
Specialized knowledge in diabetes medications, continuous glucose monitors, point of care glucometers, and insulin pump knowledge.

Nice To Haves

May have an equivalent combination of education and/or experience in lieu of specific education and/or experience as stated above.

Responsibilities

Perform critical trial-related tasks and make important trial-related decisions as directed by the Principal Investigator (PI).
Provide nutrition education and counseling for people living with diabetes.
Conduct onsite and virtual visits for patient consultations and education under the direction of the physician in charge of the clinical trial.
Assess nutritional status and provide appropriate standard of care guidance and therapy in accordance with research study protocols.
Work cooperatively with diverse, interdisciplinary departmental staff and PI to complete visits and submit accurate source documentation.
Provide education support related to diabetes medications, continuous glucose monitors, point of care glucometers, and insulin pumps to clinical trial participants.
Set appointments with subjects within the required appointment window.
Maintain all necessary licenses, certifications, credentialing materials, and other required documents.
Stay current on the latest education related to persons living with diabetes, nutrition, and food health updates.
Review and adhere to assigned research study protocols.
Maintain proper documentation and complete source documents in a timely manner.
Ensure all clinical activities are carried out in accordance with established research protocols and standards, complying with all applicable laws, regulations, policies, and procedural requirements.
Collaborate with multidisciplinary team members and Sponsor/CRO/Vendor associates.
Communicate with the participant as well as the participant’s partner/informant/caregiver.
Attend and successfully complete all training programs, including ongoing conference calls, webinars, and other professional development opportunities.
Complete provided training and Good Clinical Practice (GCP) training as required.