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Write realistic clinical vignettes and comprehensive explanations for Neurology board-style practice questions. Review and edit questions for clinical accuracy and educational value. Collaborate with the question writing team and attend team meetings.
Write realistic clinical vignettes and explanations for Psychiatry board-style practice questions. Review and edit questions for accuracy and readability. Collaborate with the medical illustration team and attend team meetings.
Develop and lead the neurology therapeutic medical strategy. Lead execution of medical affairs activities including advisory boards and medical education initiatives. Maintain high level of scientific and medical expertise.
Providing research and writing support to brand teams and new business efforts. Producing slide presentations, meeting summaries, web-based and social media materials, and peer-reviewed publications. Interacting with key experts and maintaining knowl..
Provides medical oversight of clinical trials, attends and presents at investigator and sponsor meetings, provides medical consultation to clients, investigators, and project team members, and supports business development activities.
Provide medical oversight of clinical trials, attend investigator and sponsor meetings, and provide medical consultation to clients and project team members. Manage all medical aspects of contracted tasks across the pharmaceutical product life-cycle.
Provide clinical expertise and business direction in support of medical management programs. Participate in work groups to improve health care services. Apply clinical coding and reimbursement expertise to ensure alignment with policies and practices.
Conduct coverage reviews based on individual member plan benefits and coverage policies. Document clinical review findings and outcomes. Engage with providers in peer-to-peer discussions. Interpret benefit language and policies for coverage reviews.
Lead and manage consulting projects for Veeva customers in the Medical Affairs and Medical Operations space. Develop solutions, build relationships with stakeholders, and support business development opportunities.
Collaborate with Medical Affairs colleagues to develop and execute asset strategy and tactics. Provide medical input into all aspects of product development and promotion. Track and analyze Medical Affairs tactics and performance.
Assist with virtual intake and rooming, care coordination, patient outreach, insurance navigation, and eligibility checks. Maintain medical records and documentation. Liaise with external facilities for hospital admissions and laboratory services.
As a Regional Medical Director, you will develop relationships with healthcare professionals, provide medical information, advance disease state knowledge, establish collaborations, and respond to requests for medical presentations.
Develop relationships with healthcare professionals, provide medical information, respond to presentation requests, plan territories, collaborate with professionals, mentor MSLs, identify potential investigators, and participate in training and commu..
Create regulatory-compliant documentation, conduct literature searches, write clinical study protocols and reports, and develop document strategies. Translate complex scientific information and coordinate document review process. Serve as subject mat..
Manage medical aspects of clinical trials, provide medical consultation to clients and project team members, review and analyze clinical trial serious adverse events, and provide therapeutic training and protocol training on assigned studies.
Manages medical aspects of contracted tasks across the pharmaceutical product life-cycle. Provides medical consultation, reviews adverse events, and supports clinical trial and marketed product activities. Contributes to process improvement initiatives.
Manage medical aspects of clinical trials, provide medical consultation to clients, investigators, and team members, review and analyze clinical trial adverse events, and support business development activities. MD or equivalent required.
Develop and maintain an efficient utilization management program. Educate primary care physicians on regulatory compliance. Improve market performance and analyze utilization data. Provide mentoring and leadership to physicians.
Lead medical policy development and manage medical policy committee. Serve as a coding and medical payment policy SME, develop relationships with clients, and support sales activity. Requires MD/DO with clinical and health plan experience.
Provide evidence-based medical reviews for patient care, conduct physician consultation calls, recommend alternative services or treatments, collaborate with healthcare providers for evidence-based decision making.
Perform evidence-based medical case reviews, conduct physician consultations, recommend alternative treatments, collaborate with healthcare providers, and stay current on healthcare regulations and industry developments.
Engage in scientific dialog with thought leaders, collaborate on medical strategies, facilitate research collaborations, conduct evidence read-outs, and engage with medical societies to support the development of dermatology products.
Conduct evidence-based medical reviews remotely for patient care, collaborate with healthcare providers, and recommend alternative services or treatments. Strong clinical judgment and computer skills required.
Expert cardiologist as Senior Director, Medical Affairs. Review content for accuracy, advance clinical processes, identify new market opportunities, and represent company to external stakeholders. 5+ years experience, up to 20% travel.
Coordinate and author clinical and regulatory documents. Lead submission-level documents and ensure consistency across therapeutic area documents. Contribute to strategy from a medical writing perspective.
Research, write, and edit evidence-based cancer information for professional and lay audiences. Evaluate medical literature, ensure content accuracy, and provide support for questions. Requires a medical degree with oncology specialization and excell..
Responsible for ensuring clinical excellence, driving product innovation, and providing leadership and strategic direction. Develop and implement clinical service models, oversee product development, and drive business performance to meet organizational
Establish Relationships and a Safe Learning Environment, Deliver Excellent and Engaging Synchronous Sessions, Demonstrate Fluent Use of Your Teaching Tools, Communicate and Provide Feedback Frequently
Conduct coding reviews, review flagged claims, and provide timely disposition of case referrals. Maintain knowledge of coding regulations, develop training material, and assist in educating team members on coding and policies.
Perform comprehensive medical record and claims review for Medicare Part A services. Conduct in-depth claims analysis using coding principles. Make clinical judgment decisions based on clinical experience. Meeting quality and production standards.
Perform comprehensive medical record and claims review for Medicare Part B claims. Utilize coding principles and software templates for claims analysis. Make clinical judgment decisions and ensure compliance with quality standards.
Responsible for claims payments, record maintenance, and providing counsel to claimants. Monitors and controls claims backlog and workflow, ensuring timely settlements in line with cost control standards.
Receiving and vetting medical claims, interpreting documentation, and determining payment eligibility. Providing customer support and recommendations to management. Working 40 hours per week under moderate supervision.
Develop strategic, high-quality, and medically accurate content for medical communications resources. Collaborate with internal team members to create compelling content. Review content for scientific accuracy and advise on strategic considerations.
Lead medical management programs, provide clinical expertise, and act as a liaison to network providers. Requires MD/DO with board certification and experience in Orthopedic Spine or Neurosurgery. Remote-based position with a Fortune 6 company.
Contribute to clinical development executional activities, data review, and safety management. Support regulatory submissions and planning of future studies in the rare disease area. Provide clinical expertise and input into development programs.
Clinical Research Medical Director responsible for providing clinical expertise in the development and communication of global scientific/medical evidence plans, overseeing clinical development, supporting regulatory interactions, and identifying new..
Utilize clinical expertise to review medical records and provide professional opinions on disability status. Ensure clear rationale for determinations with supporting documentation. Complete peer-to-peer calls, address quality assurance issues, and r..
Lead clinical research studies, provide clinical/scientific knowledge, interpret and communicate clinical trial data, author reports and publications, and collaborate with cross-functional teams to integrate medical, scientific, and commercial input.
Abstract E/M, CPT, HCPCS, ICD-10-CM, and modifiers from medical records. Accurately enter data into client software and perform coding using applicable guidelines and client protocols. Communicate with clients and ensure compliance with federal and s..
Chair cross-functional SRMT to review safety data, minimize risks, develop Risk Tracking Document and RMP, evaluate Benefit-Risk profiles, provide expert guidance, support inspection readiness and regulatory authority interactions.
Spending the majority of your time reviewing medical records to ensure correct diagnosis and procedure codes, performing audits for accuracy, preparing reports, providing coding insights and education, and tracking coding and billing rules.
Provide professional essay review and feedback for medical school and post-baccalaureate application components. Follow guidance and standards defined by the team and maintain regular contact. Bachelor's degree and 3 years of medical admissions experienc
The DME Coordinator supports clinical teams and beneficiaries in obtaining and placing DME, attends meetings, conducts audits, researches issues, and coordinates with vendors. Requires an Associate's degree and 3+ years of medical experience.
Identify and record correct medical codes for outpatient treatments and health services. Analyze and correct coding edits and medical necessity accounts. Provide documentation feedback to physicians. Maintain up-to-date coding knowledge and participa..
Assist Medical Director, assume clinical duties in their absence. Responsible for overseeing Case Management Program, collaborating with senior management, providing medical insight and direction. Conduct audits and provide clinical education.
Summarize medical records and enter guidelines for physicians. Review and extract electronic medical record data, create clinical summaries, and enter treatment guidelines. Communicate effectively, meet productivity requirements, and handle special p..
Review medical records and ensure accuracy of medical coding. Communicate with reviewers and office teams to address questions and provide timely quality assurance. Evaluate claims for conflict of interest and adherence to program standards.
Assist team in coordinating care for Medicare's chronic care management program. Conduct outreach calls, collaborate with clinical team, ensure data quality. Fluent in English and Spanish/Mandarin/Cantonese/Russian. Minimum 2 years healthcare experie..
Write and ensure all communications are complete and scientifically accurate. Prepare accurate, timely regulatory documents submitted to regulatory agencies worldwide. Manage writing activities across assigned projects to ensure medical writing strat..
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