Remote Senior Healthcare Jobs
3,653 Senior Healthcare jobs available for remote work from home. Apply for positions such as Palliative Oncology Nurse Navigator, Clinical Practice Performance Consultant - Remote in MD, Registered Nurse Team Lead and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The Palliative Oncology Nurse Navigator serves as a clinical resource for members with serious illness, conducting symptom assessments and facilitating advance care planning. They collaborate with care teams to monitor progress, address clinical escalations, and coordinate support plans to optimize patient outcomes.
The consultant is responsible for developing clinical partnerships to improve HEDIS quality scores and state-specific quality measures. They will conduct medical record audits, provide provider education on documentation and coding, and monitor performance metrics to ensure compliance with NCQA standards.
The Registered Nurse Team Lead oversees daily operations of direct reports while providing clinical guidance and ensuring adherence to care standards. They manage team performance, analyze clinical data, and collaborate with cross-functional partners to improve member health outcomes.
The Senior Clinical Research Associate will conduct source verification, manage site documentation, and resolve data discrepancies to ensure compliance with protocols. They will also handle budget negotiations with clinical trial sites and maintain thorough documentation of all study activities.
The VP, Clinical will lead and develop clinical operations, manage multidisciplinary healthcare providers, and oversee clinical quality metrics. They are responsible for establishing clinical protocols, optimizing day-to-day operations, and ensuring the delivery of high-quality virtual patient care.
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The Medical Science Liaison will serve as a scientific partner to clinicians in hemato-oncology, sharing clinical evidence and shaping medical strategy. They will also plan medical education events and provide expert scientific exchange regarding GSK products and clinical data.
The Clinical Specialist implements clinical programs and initiatives to support the Medication Delivery Solutions strategy while facilitating customer training and product implementation. They collaborate with regional teams to provide clinical support from pre-sale through post-conversion and maintain strong relationships with end-users.
The Clinical Specialist implements clinical business strategies and programs to differentiate the product portfolio and improve clinical outcomes. They are responsible for training, mentoring nursing staff, and managing key account relationships to ensure effective product implementation and retention.
The Regional VP is responsible for meeting and exceeding sales targets by managing, training, and developing a high-performing sales team within the assigned region. They will also cultivate strategic relationships with key accounts and Integrated Delivery Networks (IDNs) to drive profitable growth.
Manage full-cycle recruitment processes with a focus on clinical and high-volume roles while partnering with leadership to define hiring strategies. You will build candidate pipelines, leverage data to optimize recruitment, and ensure a positive experience for all stakeholders.
Leads efforts to ensure informatics systems support university objectives by translating faculty needs into technical designs. Manages systems projects from a client perspective while ensuring high levels of satisfaction and adherence to technical standards.
The Senior Oncology Patient Advocate will conduct patient advocacy sessions via video and telephone to support cancer patients with treatment decisions and resource coordination. Additionally, the role involves documenting patient interactions, assisting with workflow development, and training future advocates as the program grows.
The Director will lead and coach the MSL team to achieve scientific engagement goals while managing performance metrics and operational resources. They will also ensure cross-functional alignment with Sales and Medical Affairs to support strategic business objectives.
The Field Senior Clinical Research Associate manages clinical site monitoring activities to ensure adherence to Good Clinical Practice and regulatory guidelines. They serve as the primary point of contact for investigative sites, supporting study start-up, enrollment tracking, and data management tasks.
The coder will review provider documentation to apply accurate CPT, ICD-10, and modifier codes for OBGYN, Urology, and Primary Care specialties. They are responsible for working through EPIC work queues to resolve charge reviews, claim edits, and post-bill denials.
The Medical Director acts as a global or regional medical advisor, providing support for clinical protocols, patient safety, and eligibility determinations. They also perform medical reviews of adverse events, serious adverse events, and clinical study reports in collaboration with the pharmacovigilance department.
The Medical Science Liaison is responsible for conducting high-quality, peer-to-peer scientific exchange with healthcare stakeholders to support Eye Health objectives. They will gather actionable insights, provide disease-state education, and collaborate with internal teams to support clinical development and research.
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The Clinical Team Lead owns the clinical delivery of research trials, functioning as the project manager to ensure successful execution within budgetary and contractual requirements. They drive project strategy, manage clinical risks, oversee vendor performance, and lead high-performing teams in a matrixed environment.
Provide short-term, high-impact psychotherapy and counseling to employees and their families using evidence-based modalities. Conduct thorough clinical assessments, develop personalized treatment plans, and track progress using standardized outcome measures.
The Medical Director conducts clinical coverage reviews and renders medical necessity determinations based on benefit plans and national policies. They collaborate with multidisciplinary teams and providers to ensure the delivery of cost-effective, high-quality care while managing utilization activities.
The Sr. Manager leads cross-functional teams in the operational planning and execution of global clinical trials from start-up to closeout. They are accountable for trial-level delivery, including budget management, vendor oversight, and ensuring compliance with global health authority regulations.
The EHS Manager is responsible for implementing safety management systems, injury prevention programs, and ensuring regulatory compliance across designated divisions. They will lead incident investigations, manage DOT/FMCSA requirements, and collaborate with field leadership to drive continuous improvement in safety performance.
The Senior CRA will oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and industry standards. Responsibilities include conducting site visits, resolving issues, and collaborating with cross-functional teams to ensure accurate data collection.
The Regional Safety, Health and Environmental Manager oversees occupational safety management, policy implementation, and regulatory compliance across assigned profit centers. They are responsible for conducting safety audits, tracking performance metrics, and collaborating with regional leadership to develop strategic safety business plans.
The manager oversees the integrity and quality of safety protocols across assigned profit centers by conducting compliance audits and inspections. They also develop strategic safety plans, deliver training modules, and lead incident investigations to ensure regional adherence to safety standards.
The Clinical Operations Manager is responsible for the performance, compliance, and financial oversight of assigned clinical trial protocols within a country. They manage site budgets, clinical trial agreements, and regulatory submissions while ensuring adherence to quality standards and local regulations.
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The Clinical Research Associate conducts site monitoring visits to ensure clinical trial protocol compliance, data integrity, and adherence to regulatory standards. They provide leadership and guidance to site staff while managing study budgets, recruitment, and site-related documentation.
The Quality Analyst will validate coded data against medical documentation and act as a quality gatekeeper for outpatient coding audits. They will also provide coaching to coders, identify training needs, and contribute to process improvements to ensure compliance and accuracy.
![Pfizer is hiring for remote [MA] Amyloidosis, Field Medical Affairs Scientist](/assets/ff6c1c11-6493-422d-97ce-392ade1be20a.jpeg){kind=small}
The Field Medical Affairs Scientist acts as the primary medical and scientific point of contact for external stakeholders, including healthcare professionals and medical societies. They are responsible for developing and executing medical plans, identifying unmet medical needs, and ensuring the safe and effective use of products through high-quality scientific exchange.
The Clinical Practice Liaison builds and maintains scientific relationships with healthcare professionals to advance the company's scientific position. They provide educational outreach regarding disease states and treatment options while identifying research opportunities and supporting internal teams.
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