Clinical Research Coordinator (Contract)

Noom US

3h • $32 - $38 • Remote

About The Position

As Noom continues to expand its research initiatives, we are seeking a Clinical Research Study Coordinator (Contract) to support the execution of high-quality clinical research studies. In this hourly contract role, you will play a critical part in the day-to-day coordination and operational management of research studies, ensuring protocol adherence, regulatory compliance, and high-quality data collection.
You will partner closely with Clinical Research leadership, cross-functional stakeholders, and external partners to support study start-up, participant engagement, data tracking, and ongoing study operations. You may also help support the execution of User Research (UXR) initiatives.
This is a contract, hourly position with flexible remote work within the United States.

Requirements

• 2+ years of experience coordinating or supporting clinical research studies (industry, academic, CRO, or digital health environment); CCRC preferred
• Bachelor’s degree in public health, psychology, life sciences, or a related field (or equivalent experience)
• Strong understanding of clinical research processes, including IRB submissions, informed consent, and regulatory compliance
• Experience managing study documentation and participant-facing communications
• Exceptional organizational skills and attention to detail, with the ability to manage multiple studies or workstreams simultaneously
• Strong written and verbal communication skills
• Comfort working independently in a fast-paced, evolving environment

Nice To Haves

• Experience with digital health platforms, remote/virtual trials, or decentralized research is a plus
• Familiarity with GCP (Good Clinical Practice); CITI certification preferred

Responsibilities

• Coordinate day-to-day operations of clinical research studies from start-up through close-out
• Support study start-up activities, including documentation preparation, site coordination (if applicable), and regulatory submissions (e.g., IRB materials, amendments, renewals)
• Manage participant recruitment, screening, enrollment, scheduling, and follow-up communications
• Maintain accurate and timely study documentation, including regulatory binders and trial master files
• Ensure protocol adherence and proactively identify and resolve protocol deviations
• Track study milestones, timelines, and deliverables, escalating risks or blockers as needed
• Coordinate data collection processes and ensure high-quality data entry and management
• Serve as a point of contact for participants, ensuring a positive and compliant research experience
• Recruit participants, set up surveys, and provide support as needed for UXR projects
• Collaborate cross-functionally with Product, Data, Clinical Operations, and external vendors to support seamless study execution
• Contribute to the development and refinement of SOPs and operational workflows for future studies

Benefits

• You’ll directly contribute to the scientific validation of programs that impact millions of lives
• You’ll gain hands-on experience in digital and decentralized clinical research within a fast-growing health technology company
• You’ll collaborate with cross-functional teams shaping the future of whole-person health
• You’ll help bring operational excellence and scientific rigor to innovative, scalable health solutions

What This Job Offers

• Career Level: Mid Level