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Clinical Research Coordinator

Remote

Paradigm is rebuilding the clinical research ecosystem by enabling equitable access to trials for all patients. Our platform enhances trial efficiency and reduces the barriers to participation for healthcare providers. Incubated by ARCH Venture Partners and backed by leading healthcare and life sciences investors, Paradigm’s seamless infrastructure implemented at healthcare provider organizations, will bring potentially life-saving therapies to patients faster.

Our team hails from a broad range of disciplines and is committed to the company’s mission to create equitable access to clinical trials for any patient, anywhere. Join us, and bring your expertise, passion, creativity, and drive as we work together to realize this mission.

We are hiring a Clinical Research Coordinator  to help match patients to life-saving clinical trials. In this role, you’ll lead pre-screening—reviewing data against trial criteria, engaging with site staff, and ensuring smooth handoffs of eligible patients. You’ll also bring clinical insights back to our product and engineering teams, shaping the tools that power faster, more patient-centered trial enrollment.

What you’ll do:

  • Trial Coordination & Patient Enrollment: Oversee daily study operations, manage pre-screening, validate patient eligibility, and support smooth handoffs to sites for full screening and consent.
  • Site Engagement & Communication: Collaborate closely with site staff and investigators to optimize enrollment workflows, support feasibility assessments, and provide study updates.
  • Data & Compliance: Ensure accurate data collection, maintain patient confidentiality, and follow GCP, protocol, and regulatory standards.
  • Product Feedback & Platform Insights: Capture site-level and patient insights, track issues or improvement opportunities, and work with product/engineering teams to enhance the Paradigm platform, including NLP-driven features.
  • Site Visits & Training: Conduct site qualification visits as needed and support onboarding, training, and ongoing guidance for site teams.
  • Mentorship & Team Support: Guide junior CRCs, share best practices, and contribute to continuous improvement across the team

Who you are:

  • 3–5+ years of CRC experience, preferably in a startup or tech-forward clinical research environment
  • Strong patient-facing clinical trial experience, including recruitment, enrollment, and pre-screening.
  • Proven ability to communicate with site teams, investigators, and cross-functional stakeholders.
  • Comfort providing structured feedback to technical teams and collaborating to improve workflows and product features.
  • Excellent organizational, problem-solving, and communication skills.
  • Oncology clinical trial experience.

The base compensation range is $75,000 - $90,000. USD per year. Actual salaries will vary based on candidates' qualifications, skills, and location.

What You’ll Receive:
Paradigm Health offers a comprehensive Total Rewards package to support your well-being and success, including:
  • Competitive health, dental, and vision insurance
  • Mental health support for you and your family through Spring Health
  • Equity package
  • Unlimited paid time off (PTO)
  • 16 weeks of paid parental leave
  • Flexible work options – remote and hybrid arrangements
  • Company-paid life insurance
  • Company-paid short-term and long-term disability coverage
  • One Medical membership
  • 401(k) plan with company match

At Paradigm, we are committed to providing equal employment opportunities to all qualified individuals. We encourage and welcome candidates from all backgrounds and perspectives to apply for our open positions. We are interested in all qualified individuals and  ensure that all employment decisions are based on job-related factors such as skills, experience, and qualifications.

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