Remote Lead Healthcare Jobs
1,002 Lead Healthcare jobs available for remote work from home. Apply for positions such as Sr Manager, Medical Writing, Senior Medical Director, Product Safety Physician Lead, Regional Chief Nursing Officer and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The Senior Manager will independently author and finalize complex regulatory documents to support clinical development programs and FDA interactions. They will collaborate with cross-functional teams to ensure scientific accuracy and compliance with regulatory standards.
The Senior Medical Director serves as the Lead Product Safety Physician for complex developmental programs, overseeing the benefit/risk safety profile throughout the product life cycle. They are responsible for managing safety concerns, leading safety management teams, and ensuring regulatory compliance through effective communication and data analysis.
The Regional Chief Nursing Officer oversees nursing quality, regulatory compliance, and clinical outcomes across multiple hospitals within the region. They provide leadership, training, and strategic support to local CNOs and the regional executive team to ensure operational excellence.
The Professional Services Veterinarian acts as a technical expert and coach, supporting territory managers by delivering technical lectures and developing business strategies. They collaborate with internal teams and external stakeholders to promote the company's animal health portfolio and improve customer medical capabilities.
The Therapeutic Strategy Director leads cross-functional teams to design innovative, client-centric solutions for internal medicine programs during the proposal and business development phase. They are responsible for securing new business, managing high-level client relationships, and ensuring the successful translation of strategy into operational delivery.
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The Vice President of Clinical Development will provide strategic and operational leadership for global ophthalmic genetic medicine programs, serving as the primary medical monitor for clinical trials. They are responsible for overseeing clinical study design, regulatory document preparation, and cross-functional collaboration with internal and external partners.
The Medical Director leads care, case, and utilization management programs by setting clinical standards and driving operational performance. They are responsible for managing clinical teams, designing care models, and partnering with cross-functional stakeholders to achieve population health outcomes.
The Clinical Operations Development Lead co-leads the Clinical Development Team and is accountable for the strategic execution of clinical programs within agreed budgets and timelines. They oversee clinical trial activities, manage vendor relationships, and ensure compliance with regulatory standards throughout the compound lifecycle.
Provide evidence-based psychotherapy, assessments, and diagnoses for OCD patients via a video platform. Manage a caseload, maintain clinical documentation, and collaborate with a network of providers to reinforce treatment decisions.
Provide diagnostic assessments and evidence-based psychotherapy for trauma and PTSD patients via a remote video platform. Manage caseloads, maintain clinical documentation, and collaborate with a network of providers to reinforce treatment decisions.
The EHS Manager is responsible for the global oversight, standardization, and alignment of the organization’s EHS framework across international aviation operations. This role develops global policies, monitors regional conformance, and supports independent assurance activities to ensure safety and regulatory compliance.
The Director of Clinical Affairs will lead the clinical study program, formulating evidence generation strategies and overseeing the planning, implementation, and reporting of clinical studies. They will collaborate with cross-functional teams to ensure regulatory compliance and drive the global market access of the company's neuromodulation therapy.
The Head of Clinical and Medical Affairs will lead global clinical research and evidence generation strategies while overseeing medical activities and scientific communications. This role involves building and managing a high-performing team to bridge internal functions with the external scientific community.
The Director of Clinical Quality Assurance leads strategic quality objectives and ensures clinical research activities comply with global GCP regulations and Jazz standards. This role manages vendor performance, drives inspection readiness, and collaborates cross-functionally to mitigate risks and improve clinical processes.
Lead clinical informatics activities for federal and state interoperability initiatives while translating clinical workflows into technical requirements. Facilitate collaboration among diverse stakeholders including clinicians, public health agencies, and software engineering teams to deliver scalable solutions.
The consultant manages a block of stop loss business, overseeing new business and renewal pricing, risk analysis, and financial performance. They collaborate with sales, clinical, and underwriting teams to develop creative solutions and provide leadership and training to staff.
You will provide medical leadership and strategic direction for clinical development programs while ensuring study protocols are scientifically sound and regulatory compliant. Additionally, you will interpret clinical trial data to guide development strategies and build relationships with key opinion leaders and investigators.
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The Senior Director is responsible for the strategic operational planning and clinical performance of the Hematology franchise, including managing the Global Clinical Program Lead and Study Manager groups. They act as a key representative for clinical operations, driving therapeutic strategy and ensuring execution excellence across global clinical programs.
The Medical Science Liaison will execute field medical plans, engage in peer-to-peer scientific exchange with healthcare professionals, and gather medical insights within the UK territory. They will also support clinical study site engagement and collaborate cross-functionally with internal teams to advance the company's oncology pipeline.
The Associate Director will provide end-to-end leadership for clinical data management across assigned studies, from protocol review through database lock and regulatory submission. They will oversee CROs and vendors while ensuring high-quality, analysis-ready data in compliance with GCP and regulatory standards.
The Physician Executive will serve as a strategic partner within the commercial team, providing clinical expertise to support sales and customer engagement. They will act as a bridge between clinical practice and technology, ensuring solutions meet real-world needs while advocating for clinicians.
The Executive Medical Director will lead the global clinical development strategy for solid tumors, specifically focusing on the breast cancer product Elacestrant. Responsibilities include overseeing Phase 1-4 clinical studies, managing multi-disciplinary teams, and ensuring successful regulatory submissions.
The Section Head will lead the Chest Radiology department, overseeing diagnostic and treatment procedures while collaborating with multidisciplinary teams. The role involves participating in academic activities, including research, teaching, and the integration of AI and natural language processing technologies.
The Healthcare Solutions Partner will drive go-to-market execution and manage strategic client relationships within the healthcare and life sciences sector. They will collaborate with account executives to identify business opportunities and provide domain expertise to support complex deal cycles.
The Head of Safety, Health & Environment will lead EHSS strategy and readiness activities for U.S. small molecule growth projects. This role involves overseeing regulatory compliance, process safety, and sustainability programs throughout the design, construction, and operational phases.
Lead the development and implementation of clinical operations excellence strategies, ensuring GCP compliance and quality across global clinical trials. Manage cross-functional teams and processes, including eTMF oversight, performance metrics, and continuous improvement initiatives.
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Provide virtual, 1:1 nutrition counseling to patients with eating disorders using a weight-inclusive and trauma-informed care model. Collaborate with a multidisciplinary care team and maintain accurate, timely clinical documentation.
Collaborate on the design of clinical research studies and develop biostatistical analysis plans for research proposals and grants. Manage, analyze, and interpret study data while educating research team members on statistical methods.
The Digital Health Engagement Partner is responsible for driving the adoption and sales of Rejoyn within health systems and integrated delivery networks. This role involves executing strategic account plans, engaging clinical stakeholders, and ensuring seamless integration and utilization of the digital therapeutic.
The EHS Manager is responsible for the global oversight, standardization, and alignment of the organization’s EHS framework across international aviation operations. This role coordinates EHS policy, monitors performance, and supports independent assurance activities to ensure organizational conformance.
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