Browse and apply for latest Remote Healthcare Jobs and work remotely at over 1000+ companies hiring now. Explore remote healthcare careers amd work from home in nursing, medical billing, medical coding for telecommuting positions like Senior Coder, Nurse Coach, Manager, Pharmacy and Medicare Compliance.
Trusted by 200,000+ remote workers worldwide.
The Senior Manager, Clinical Operations acts as the Clinical Process Owner, responsible for the governance, harmonization, and lifecycle management of clinical operations SOPs and documentation. They lead cross-functional initiatives to ensure processes are compliant, scalable, and effectively implemented across the organization.
The Senior Manager, Clinical Operations serves as the Clinical Process Owner, responsible for the governance, harmonization, and lifecycle management of clinical operations processes. They lead cross-functional initiatives to ensure processes are compliant, scalable, and effectively implemented across the organization.
The Senior Clinical Research Associate will act as a subject matter expert, providing mentorship and performance feedback to peers while overseeing site monitoring and study integrity. They will also manage monitoring services for complex projects, assist in hiring and training, and serve as the primary escalation point for site or patient issues.
The Senior Clinical Trial Manager provides leadership and direction to clinical site management teams while overseeing regional CTMs and coordinating study activities. They are responsible for developing monitoring strategies, managing budgets, and ensuring compliance with clinical protocols and regulatory requirements.
The Clinical Payments Specialist manages end-to-end global investigator payments, including setup, deployment, and reconciliation of study payment solutions. They act as a liaison between investigative sites and clinical teams while ensuring payments align with clinical trial agreements and budgetary forecasts.
We watch for new remote healthcare jobs and email you the matches. Free. Unsubscribe in one click.
The Clinical Payments Specialist manages end-to-end investigator payments, including setup, deployment, and reconciliation for assigned studies. They act as a liaison between investigative sites and internal teams while ensuring payments align with clinical trial agreements and budgetary forecasts.
The Medical Director provides medical leadership for clinical trials, including protocol development, medical monitoring, and safety evaluation. They serve as the primary medical liaison between the sponsor and internal departments to ensure study compliance and effective issue resolution.
The Senior Decentralized Clinical Trial Study Lead is responsible for the strategic development and delivery of decentralized clinical trials, ensuring they meet quality, speed, and financial objectives. They act as the primary point of contact for customers and lead cross-functional teams to manage study milestones, risks, and project performance.
The Associate Manager is responsible for interviewing, selecting, and onboarding CRA/IHCRA candidates while ensuring they are properly trained and mentored. They also manage performance, review quality metrics, and act as a point of escalation for project-related issues.
The clinician will remotely administer semi-structured clinical interviews and cognitive assessment batteries to study subjects. They are also responsible for scoring assessments and providing central monitoring reviews to ensure data accuracy.
The Medical Director will provide expert medical monitoring and leadership for clinical research projects, ensuring compliance with protocols and safety standards. They will also support business development, mentor junior staff, and maintain strong consultative relationships with clients.
The incumbent will lead medical science and strategy for metabolic clinical research, providing expert input on development plans, regulatory issues, and clinical trial protocols. They will also engage in business development, support client proposals, and mentor internal clinical teams to ensure high-quality delivery of research projects.
The incumbent will lead medical science and strategy for oncology, driving business outcomes through proposal development, client engagement, and strategic clinical trial design. They will also provide therapeutic expertise to internal teams, mentor clinical scientists, and contribute to innovative clinical research initiatives.
The Medical Director serves as the Global Lead Medical Monitor for clinical trials, providing therapeutic expertise and protocol-specific training to project teams. They also contribute medical input to clinical development programs and support business development activities through proposal generation and sponsor meetings.
Perform manual, independent reviews of clinical trial interviews to ensure scoring accuracy, interview quality, and protocol adherence. Maintain clear documentation of review findings and scoring justifications while overseeing site performance and rater remediation.
The Safety Physician provides medical and operational oversight for end-to-end pharmacovigilance activities, including ICSR medical assessment and coding standards. They also lead quality control initiatives, support benefit-risk strategies, and act as a primary point of contact for cross-functional medical review requirements.
The Senior Clinical Team Manager directs and coordinates the technical and operational aspects of clinical trials to ensure successful completion within budget and timelines. They manage clinical and start-up activities, lead project teams, and maintain compliance with ICH GCP and regulatory standards.
We watch for new remote healthcare jobs and email you the matches. Free. Unsubscribe in one click.
The Clinical Specialist reviews clinical trial data and assessment scales to ensure standardized practices and data integrity. They also provide guidance to raters through live interactions, feedback, and functional assessments.
The Clinical Specialist supports stroke clinical trials by administering standardized assessments and ensuring data quality. They also review assessments conducted by other raters to maintain protocol compliance and provide feedback on scoring techniques.
The translator will perform translation and localization tasks within the life sciences, medical, and clinical trials domains. They are expected to contribute to AI and language technology projects while maintaining high quality standards.
The Clinical Team Manager oversees all clinical operational and quality aspects of respiratory studies in compliance with ICH-GCP. This includes developing monitoring strategies, managing project financials, and leading clinical teams to ensure deliverables are met within contractual timelines.
Responsible for the development, coordination, and implementation of Phase 1 clinical research studies, including site management and monitoring oversight. The role involves tracking study progress against milestones, managing resource allocation for CRAs, and ensuring regulatory compliance and data integrity.
Provide high-quality medical information services via phone and email, answering technical product questions and handling adverse event reports. Translate medical documents between English and Spanish and ensure all inquiries are logged accurately in compliance with SOPs.
Provide high-quality mental health support through psychotherapy, counseling, or coaching sessions to clients in the Asia-Pacific and Europe regions. Responsibilities also include leading support groups and delivering educational Masterclasses.
Provide medical leadership and support for clinical trials, including the creation of protocols and real-time medical monitoring of study subjects. Serve as the primary medical liaison between the sponsor and internal departments to ensure study compliance and safety.
Provide strategic medical and scientific expertise in hematology-oncology to support proposal development, protocol design, and clinical development plans. Act as a subject matter expert and consultant throughout the research and development lifecycle to guide project teams and sponsors.
We watch for new remote healthcare jobs and email you the matches. Free. Unsubscribe in one click.
Design and implement statistical strategies and analysis plans for clinical trials across various therapeutic areas. Perform SAS programming to generate study reports and provide expert guidance on methodology and sample size calculations.
Provide medical leadership and support for clinical trials in nephrology, including protocol creation and real-time medical monitoring. Act as the primary medical liaison between the sponsor and internal departments to ensure subject safety and study compliance.
The Director will engage with senior management to establish strategic department initiatives and drive business development activities for Clinical Assessment Technologies. They are also responsible for overseeing the development of assessment training content and ensuring all materials meet protocol and regulatory requirements.
Stop the endless job search. Our AI finds and applies to the best jobs for you.
Learn more about Healthcare remote jobs
