36,017 Medical jobs available for remote work from home. Apply for positions such as Senior Technical Implementation Partner, Opportunity Development Specialist, Triage Nurse, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The Senior Technical Implementation Partner will manage enterprise-wide software deployments, focusing on the Inpatient Capacity solution. They will collaborate with cross-functional teams and hospital stakeholders to ensure successful project lifecycles, tool adoption, and measurable business outcomes.
The Opportunity Development Specialist is responsible for generating new business opportunities through outbound outreach and facilitating client introductions to the sales team. They will collaborate with field sales to develop target lists, manage CRM records, and track performance metrics to meet revenue goals.
The Triage Charge Nurse provides comprehensive clinical care through telehealth triage, assessment, and intervention to promote offender health and safety. The role also involves administrative leadership, including mentoring staff, maintaining clinical records, and coordinating care across multiple correctional sites.
Perform site management activities in compliance with SOPs, regulatory guidelines, and study protocols to ensure audit readiness. Manage site-level communication, data review, and investigator training while supporting patient recruitment and retention strategies.
The specialist is responsible for encoding adverse events, medical history, and medications using industry-standard dictionaries like MedDRA and WHOdrug. They also collaborate with clinical and data management teams to ensure coding consistency and timely processing of project data.
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The Clinical Trial Manager II is responsible for site management oversight, clinical monitoring, and ensuring protocol compliance and data integrity throughout the study lifecycle. They also manage study risks, coordinate with functional teams, and oversee the performance of CRAs and Central Monitors to meet project milestones.
The Clinical Project Manager oversees interdisciplinary clinical research programs, ensuring compliance with GCPs and regulatory requirements while managing project timelines and budgets. They act as the primary liaison between the company and the customer, leading clinical teams and facilitating project delivery from launch to closeout.
The Principal Medical Writer will lead clinical documentation efforts and manage complex regulatory submissions. They will collaborate with cross-functional teams to ensure high-quality deliverables that meet customer needs and regulatory standards.
The Lifecycle Marketing Manager will develop and optimize multi-channel customer communications across the user lifecycle, including onboarding, engagement, and retention. They will manage end-to-end campaign execution, from strategy and creative briefing to data-driven analysis and A/B testing.
The Account Manager is responsible for developing and executing strategic business plans to drive sales and revenue within an assigned territory. They must build strong relationships with institutional stakeholders and collaborate cross-functionally to increase product access and adoption.
The Licensing Coordinator I manages the state licensing process for practitioners, including collecting documentation and submitting applications to licensing boards. They also track application statuses and maintain accurate records within the credentialing database.
The Lead Casualty Claims Adjuster will proactively manage complex casualty claims from initial notice to resolution, including coverage analysis and litigation oversight. The role also involves mentoring less experienced adjusters and providing technical advice to leadership and underwriting.
The Senior Immigration Attorney will develop sophisticated legal strategies and represent clients in complex immigration matters before USCIS, EOIR, and other agencies. Additionally, the role involves mentoring associate attorneys, overseeing legal quality, and partnering with executive leadership to support the firm's California expansion.
The Global Supply Chain Director will oversee and manage international supply chain operations, including procurement, logistics, and inventory management. They are responsible for developing strategic initiatives to drive efficiency, mitigate risks, and ensure compliance with global standards.
The Team Leader will provide disciplinary and professional leadership to a team of 10-15 customer service agents. Responsibilities include monitoring performance KPIs, conducting coaching sessions, and ensuring service quality standards are met.
Conduct on-site inspections and assessments of residential and commercial property damages to determine claim validity. Collaborate with policyholders and stakeholders to negotiate and settle claims while providing exceptional customer service.
The Coordinator II serves as the primary point of contact for pharmaceutical companies and research organizations to facilitate IRB review processes. They are responsible for conducting administrative reviews of protocol submissions and ensuring accurate, timely communication with clients.
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The Clinical Lead oversees site activation timelines, quality, and deliverables while coordinating with internal teams and functional leads. They also manage study budgets, monitor activation status, and provide progress updates to clients and management.
The position provides itinerant early intervention services to infants and toddlers with hearing loss in their natural environments. Responsibilities include developing Individualized Family Service Plans, conducting language assessments, and providing developmentally appropriate instruction.
Perform regulatory inspections and complaint investigations of nursing homes to ensure compliance with federal and state requirements. Document findings, prepare statements of deficiency, and coordinate with facility staff to ensure timely resolution of issues.
The specialist monitors county child welfare programs to ensure compliance with federal and state regulations while providing technical assistance and coaching. They analyze program data and performance metrics to support continuous quality improvement and effective service delivery across a multi-county region.
The Nurse Consultant conducts on-site surveys and documentation reviews to license and certify health care providers and suppliers. They provide regulatory oversight by investigating complaints and ensuring compliance with state and federal Medicare/Medicaid standards.
The Regulatory Affairs Manager will lead and support regulatory submissions and life-cycle management procedures within Latin American markets. They will act as a local regulatory expert, coordinating strategy and ensuring compliance with regional health authority requirements.
Leads the preparation and completion of complex clinical medical writing deliverables while ensuring scientific accuracy and regulatory compliance. Coordinates cross-functional activities and mentors junior staff to ensure projects are delivered on time and within budget.
The Site Care Partner performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and support patient recruitment and retention strategies.
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The Project Manager oversees interdisciplinary clinical research studies, ensuring compliance with GCP and regulatory requirements while managing project timelines and budgets. They act as the primary liaison between the company and the customer to ensure successful study delivery and foster strong client relationships.
The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and maintain essential study documentation throughout the clinical trial lifecycle.
The CRA II is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and maintain essential study documentation.
The GAD Coordinator oversees a team of Member Services Representatives to ensure member inquiries are addressed and service providers are identified. This role focuses on intake for Part C and D pre-service appeals while maintaining accurate membership records and databases.
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