Full-Time

Clinical Trials Dietitian

Clinical Trials Unit

Posted on 10/1/2025

Deadline 10/21/25
Louisiana State University (LSU)

Louisiana State University (LSU)

No salary listed

Company Does Not Provide H1B Sponsorship

Baton Rouge, LA, USA

In Person

Category
Medical, Clinical & Veterinary (1)
Requirements
  • Bachelor’s degree in Dietetics, Nutrition, or a related field.
  • Registered Dietitian (RD) or Registered Dietitian Nutritionist (RDN) credential by the Commission on Dietetic Registration (CDR).
  • Strong organizational skills with the ability to manage multiple tasks and timelines.
  • Excellent written and verbal communication skills.
  • Compassionate, non-judgmental approach to working with diverse populations.
  • Proficiency in Microsoft Office Suite (Word, Excel, Outlook, PowerPoint).
Responsibilities
  • Conduct comprehensive assessments of participants’ dietary intake, nutritional status, and health behaviors using validated tools and methodologies.
  • Collaborate in the design and delivery of nutrition and health promotion interventions tailored to specific study protocols.
  • Support study start-up activities, including protocol review, staff training, and preparation of study materials.
  • Develop and maintain study-specific documentation such as source documents, screening tools, phone scripts, and data collection forms.
  • Assist in creating and refining project workflows, recruitment strategies, and standard operating procedures to ensure efficient trial execution.
  • Lead or support informed consent processes, ensuring participants understand study procedures and requirements.
  • Perform study visits and collect protocol-specific data, including anthropometric measurements, dietary recalls, and other clinical assessments.
  • Manage and oversee accurate and timely entry of clinical trial data into electronic data capture systems.
  • Deliver specialized nutrition-related procedures or interventions as outlined in study protocols, including meal planning, counseling, or metabolic testing.
  • Coordinate operational aspects of clinical trials, including regulatory submissions, budget monitoring, and timeline management in collaboration with the research team.
Desired Qualifications
  • Master’s degree in Nutrition, Dietetics, Public Health, or a related field.
  • One (1)– Three (3) years of experience working in clinical research, clinical trials, or healthcare settings.
  • Familiarity with Institutional Review Board (IRB) processes and Good Clinical Practice (GCP) guidelines.
  • Experience with electronic data capture systems (e.g., REDCap).
  • Knowledge of clinical trial design, protocol development, and regulatory compliance.
  • Experience conducting nutrition assessments and interventions in diverse populations.
  • Ability to interpret and apply scientific literature to clinical practice.
  • Strong analytical skills and experience with data collection and reporting.
Louisiana State University (LSU)

Louisiana State University (LSU)

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