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RDs for Obesity Trial – Telehealth Role

Remote, USA Full-time Posted 2025-11-03
POSITION SUMMARY: RapidTrials is seeking experienced and credentialed Registered Dietitians (RDs) to support a Sponsor’s Phase 3 clinical trial targeting weight management in obese and overweight adults with and without type 2 diabetes. Dietitians will provide telehealth-based patient support across multiple time zones in the U.S., contributing to participant retention and protocol compliance by delivering standardized nutritional guidance aligned with trial protocols. Number of Positions: 1 Position Type: Contractor / Freelance (no benefits included; expenses not reimbursed) Position Reports To: Site-Assigned Investigator / Designee Duration of Contract: Approximately 20 months’ Work Hours: Flexible between 7 AM – 6 PM (Local Time); estimated +/- 6 hours per participant across 8 visits Setting: Remote (Telehealth services across U.S. states) Locations: New Hampshire Start Date: ASAP KEY RESPONSIBILITIES: • Conduct scheduled telehealth visits with study participants over a 20-month period (8 visits per participant; first visit ~60 minutes, subsequent ~30 minutes) • Provide protocol-aligned nutritional counseling and education related to weight loss and obesity management • Maintain appropriate documentation of each visit; submit visit summaries to clinical sites • Participate in sponsor protocol training, site-specific onboarding, and attend weekly status update calls • Maintain licensure and certification as required per state laws • Ensure timely response to communications, maintain appointment punctuality, and escalate any protocol deviations to site personnel • Maintain a professional demeanor in all patient and site interactions • Flexible schedule to accommodate telehealth visits based on participant availability. ELIGIBILITY REQUIREMENTS: • Active Registered Dietitian credential • Licensure/certification in New Hampshire, • Strong verbal communication skills in English • Experience in telehealth delivery • Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements. • Certificate of completion for Good Clinical Practices (GCP)/International Conference on Harmonization (ICH) training, and HIPAA training completed in the past 24 months. • Proficiency with Microsoft products, including but not limited to word-processing software • Must have access to a private, professional work setting with high-speed internet and HIPAA-compliant communication capabilities • Access to and experience with a legal and regulatory compliant telehealth platform for visit conduct. • Comply with all HIPAA, privacy, and confidentiality standards • Able to sign Business Associate Agreement (BAA) and site Delegation of Authority (DOA) forms as required • • Currently authorized to work in the United States • Bilingual, a plus APPLICATION PROCESS: Candidates must complete an online application and provide licensure information, availability, and upload relevant credentials. Apply Job! Apply to this Job

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