Remote Healthcare administration Jobs · Regulatory Compliance

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  • Conduct clinical audits, risk assessments, and process reviews to identify compliance gaps and improvement opportunities.
  • Manage multiple client engagements and collaborate with healthcare client teams to ensure successful project execution.
  • Prepare and present audit results and recommendations to clinical, operational, and executive leadership.

Kodiak Solutions provides technology-driven solutions for healthcare finance, risk management, and revenue cycle management. The company's size and culture are not disclosed in the posting.

  • Own and manage multi-state provider licensing, ensuring zero lapsed licenses.
  • Run the full new-state licensing process, including vendor and board communication.
  • Maintain a real-time system of record for provider license status and compliance.

Honeydew builds clinical infrastructure to connect patients with providers quickly and reliably. They have helped over 40,000 patients and are growing 5x year over year.

  • Provide strategic leadership and operational oversight for care management functions across the assigned region.
  • Ensure alignment with systemwide standards and regulatory requirements for hospital Care Management.
  • Collaborate with leadership to formulate strategies that drive organizational objectives and patient-centered outcomes.

CommonSpirit Health is a nonprofit Catholic healthcare organization delivering integrated health services through a network of hospitals, clinics, and care sites across 24 states. With over 157,000 employees and 25,000 physicians, it is one of the largest nonprofit healthcare systems, committed to creating a more just and equitable healthcare delivery system.

  • Lead site activation strategies and oversee start-up activities across clinical studies.
  • Manage critical path plans and mitigate risks to ensure timelines are met.
  • Collaborate with cross-functional teams and clients to improve activation processes.

Our partner is a clinical research organization that supports the delivery of clinical trials. They are a global company with a collaborative culture focused on innovation and operational excellence.

  • Review emergency department medical records to assign accurate ICD-10-CM, CPT, and HCPCS codes.
  • Ensure compliance with coding guidelines, CMS regulations, and payer-specific requirements.
  • Collaborate with coding leadership and participate in quality reviews and audits.

Sutherland works with iconic brands worldwide, providing market-leading technology and business process excellence. The company has created over 200 unique inventions and focuses on AI, automation, and cloud engineering.

$152,600–$283,400/yr

  • Deliver accurate and empathetic education to patients and caregivers about Duchenne Muscular Dystrophy and Spinal Muscular Atrophy.
  • Build relationships with advocacy organizations and attend live and virtual events, including weekend engagements.
  • Provide insights from patient interactions to shape cross-functional strategies and educational materials.

Novartis is a pharmaceutical company focused on innovative science to improve the lives of people living with disease. The company is committed to creating an inclusive workplace and offers a comprehensive benefits package.

  • Provide study oversight as primary liaison between CRAs, internal staff, site staff, client personnel, and external vendors.
  • Ensure clinical monitoring activities comply with SOPs, regulations, GCP, KPIs, and study-specific requirements.
  • Develop and manage clinical plans and guidelines, including the clinical monitoring plan and study timelines.

ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996, supporting research behind innovative treatments in pharmaceutical, biotech, and medical device industries. They foster a collaborative community where team members feel valued, supported, and empowered to make a meaningful impact on global health.

$65,450–$90,000/yr
US 4w PTO

  • Support Clinical Trial Managers in the day-to-day execution of clinical trials from start-up through close-out.
  • Own critical study coordination workflows such as maintaining trackers, decision logs, and training records.
  • Ensure study documentation and training records are complete, current, and audit-ready.

Oura is a health technology company that produces the Oura Ring, a wearable device for tracking sleep, activity, and readiness. It is a quickly growing company with a mission-driven culture focused on employee well-being and innovation.

$109,000–$174,800/yr

  • Serve as a subject matter expert for site management and monitoring strategies across complex clinical studies.
  • Collaborate with clinical teams, investigators, and stakeholders to ensure compliance, data quality, and trial success.
  • Mentor CRA staff, resolve escalated issues, and support site qualification, initiation, monitoring, and close-out visits.

Jobgether is a platform that uses AI-powered matching to connect candidates with job opportunities. They operate as a global healthcare and technology environment, offering professional growth and innovative solutions.

  • Perform in-house and remote monitoring activities for clinical trials, ensuring compliance with regulatory requirements and study protocols.
  • Support study start-up, site selection, and document tracking while assisting CRAs with on-site and remote monitoring.
  • Communicate with investigative sites to resolve queries and maintain study tracking tools for deviations, SAEs, and data discrepancies.

Jobgether is an AI-powered job matching platform that connects candidates with hiring companies. The environment is collaborative, international, and focused on improving patient outcomes through high-quality research.