1099 Dietician

Overview

Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.

As an employee of Velocity, you are the most integral part of our mission. For talented candidates who perform at a high level, Velocity will invest to support career advancement and reward performance. Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity.

Benefits include medical, dental and vision insurance, paid time off and company holidays, 401(k) retirement plan with company-match, and an annual incentive program.

Job Summary:

The Clinical Research Dietitian will provide nutritional expertise and support for clinical trials focused on obesity, metabolic health, and related interventions. This role involves developing and implementing dietary protocols, counseling study participants, monitoring compliance, and collaborating with interdisciplinary research teams to ensure high-quality data collection and participant support.

Responsibilities

Duties/Responsibilities:

• Design, implement, and monitor dietary plans aligned with clinical trial protocols and study objectives
• Provide one-on-one and group nutrition counseling to study participants, focusing on weight management, behavioral change, and lifestyle modification
• Support participant recruitment and screening with emphasis on nutritional eligibility criteria
• Monitor dietary adherence, maintain accurate records, and support data collection for nutritional outcomes
• Collaborate with investigators, coordinators, and other clinical operations staff to optimize study design and participant experience
• Ensure all documentation complies with regulatory standards, including IRB-approved protocols and Good Clinical Practice (GCP)
• Contribute to the preparation of study reports, publications, and presentations related to nutritional findings
• Other duties as assigned

Qualifications

Required Skills/Abilities:

• Strong understanding of clinical trial data collection, GCP guidelines, and regulatory requirements.
• Excellent analytical skills and attention to detail to ensure data accuracy and compliance.
• Ability to work independently and collaboratively in a fast-paced clinical research setting.
• Primarily overnight shifts; occasional daytime studies or meetings
• Clinical research setting; some participant-facing responsibilities may require early morning or evening availability
• Hybrid work environment may be available depending on study design and site policies

Education and Experience:

• Bachelor’s degree in Nutrition, Dietetics, or related field required; Master’s degree preferred
• Registered Dietitian (RD/RDN) credential required
• Minimum of 2 years of experience in clinical nutrition; prior experience in clinical research or obesity-focused interventions strongly preferred
• Familiarity with GCP, IRB processes, and regulatory documentation
• Excellent communication, counseling, and documentation skills
• Experience with dietary software, data entry, and Microsoft Office Suite

NOTE: The above Job Description is intended to communicate the general function of the mentioned position and by no means should be considered an exhaustive or complete outline of the specific tasks and functions that will be required.  Additionally, specific tasks and duties of the position are subject to change as the Company, the department and circumstances change.  All employees are expected to perform their duties within their ability as required by the job and/or as requested by management.