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CareDx

Noninvasive transplant diagnostics and patient monitoring

Senior Clinical Research Associate

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeRemote in USA

About the Job

Requirements

  • A bachelor's degree or higher in biomedical sciences or a related field.
  • At least 5 years of experience in clinical research within biotech, pharma, medical device, or academia.
  • Strong knowledge of Good Clinical Practice (GCP), Food and Drug Administration regulations, and International Organization for Standardization standards.
  • Proficiency in electronic data capture (EDC) systems, clinical trial management systems (CTMS), and Microsoft Office Suite.
  • A strong understanding of medical terminology and clinical trial processes.
  • Ability to manage multiple studies and priorities with precision and urgency.
  • Ability to work independently and collaboratively in remote, cross-functional teams.
  • Ability to travel up to 75% of the time.

Responsibilities

  • Conduct and oversee site selection, initiation, interim, and close-out visits to ensure protocol adherence, patient safety, and data accuracy.
  • Collaborate with principal investigators, study coordinators, and cross-functional teams to drive study success.
  • Ensure compliance with GCP, institutional review board requirements, and internal monitoring plans.
  • Identify and resolve data collection issues within EDC systems.
  • Review and reconcile data queries, listings, and discrepancies.
  • Maintain accurate and complete study documentation and files.
  • Lead study team meetings and contribute to protocol development and amendments.
  • Support site recruitment and provide oversight to ensure enrollment goals are met.
  • Mentor junior clinical research associates and provide technical expertise in clinical programming and data validation.
  • Assist in developing and refining standard operating procedures, workflows, and templates.
  • Partner with the clinical trials manager to manage timelines, budgets, and resources.
  • Liaise with regulatory authorities and contract research organizations as needed.
  • Ensure timely and compliant execution of monitoring reports, trip reports, and follow-up letters.
  • Monitor site performance metrics and facilitate effective communication across stakeholders.

Desired Qualifications

  • Certification as a Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Associate (CCRA) is a plus.

About the Company

CareDx

Noninvasive transplant diagnostics and patient monitoring

CareDx provides noninvasive tests and digital tools to support people who receive organ transplants. It offers kidney transplant services, HLA typing for organ matching, and digital platforms to manage transplant care from pre-transplant diagnostics to post-transplant monitoring. It also collaborates with biopharma companies to speed clinical development through its pharma services. The products work by using noninvasive tests to monitor transplant health and by providing software that helps doctors, patients, and caregivers track appointments, results, and treatment plans. Unlike many competitors, CareDx combines testing, data management, and patient support in one integrated system and works with pharma partners, focusing on the full transplant journey rather than just a single piece. The goal is to improve transplant outcomes and patient experiences by making testing and care easier, more accurate, and more coordinated.

Company size
51-200
Company stage
IPO
Headquarters
Brisbane, CA
Founded
2000

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