Medical Jobs

Discover remote medical opportunities worldwide. We've gathered the top positions to help you advance your career.

Medical
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πŸ“ India

πŸ” Biopharmaceutical

🏒 Company: Praxis Precision Medicines, Inc.

  • Bachelor’s degree in a scientific discipline; advanced degree, CNS, and Rare Disease experience is a plus.
  • Minimum 3 years of medical writing experience in a Sponsor or CRO setting.
  • AMWA certification preferred.
  • Experience with medical writing systems and technologies like Veeva RIM.
  • Knowledge of drug development, ICH guidelines, and FDA/EU guidance.
  • Self-motivated, autonomous, and able to contribute to collaborative teams.
  • Highly organized, detail-oriented, with strong communication skills.

  • Implements medical and regulatory document preparation activities, serving as writing lead or coordinating with external writers.
  • Supports documents for regulatory submissions including INDs, NDAs, MAAs, protocols, investigator brochures, and clinical study reports.
  • Collaborates with cross-functional teams to ensure the timely completion of quality documents and publications.
  • Supports clinical trial transparency including registration and results posting on databases like clinicaltrials.gov.
  • Contributes to departmental development through editorial support for templates and standard operating procedures.

CollaborationQuality AssuranceEditing

Posted 3 days ago
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πŸ“ United States of America

πŸ’Έ 57700.0 - 107800.0 USD per year

πŸ” Healthcare

🏒 Company: highmark

  • Bachelor’s degree in nursing or a Master’s degree in Social Work, Counseling, Education, or a related field.
  • 3 years experience in Acute or Managed Care/experience with Medicaid or Medicare populations, or 5 years experience for Social Work.
  • Preferred experience with high-risk pregnant women or chronic conditions.
  • Bilingual English/Spanish language skills and Case Management Certification.

  • Ensure members with complex needs have access to high-quality, cost-effective healthcare.
  • Facilitate assessment, planning, coordination, monitoring, and evaluation of healthcare services.
  • Educate members on illness impacts and collaborate with healthcare providers to coordinate care.
  • Develop individualized care plans and adjust goals based on monitoring.
  • Participate in interdisciplinary meetings and maintain knowledge of community resources.
Posted 3 days ago
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πŸ“ UK

πŸ’Έ 35000.0 - 45000.0 GBP per year

πŸ” Life sciences

🏒 Company: SorceroπŸ‘₯ 51-100πŸ’° Series A over 3 years agoArtificial Intelligence (AI)PaaSMachine LearningEnterprise SoftwareHealth CareNatural Language ProcessingSoftware

  • PhD in a relevant medical or life sciences discipline.
  • Minimum 5 years of professional experience in medical writing.
  • Proven track record in Plain Language Summary development.
  • Experience in customer service and client-facing roles.
  • Extensive experience in clinical research publication processes.
  • Advanced understanding of medical terminology and scientific writing principles.
  • Broad experience with AI-powered content development platforms.
  • Advanced proficiency in systematic review methodologies.
  • Expert knowledge of publication management systems.
  • Strong digital literacy and computational skills.
  • In-depth understanding of EMA and FDA regulatory guidelines.

  • Lead the development of Plain Language Summaries (PLS) from Clinical Study Reports (CSRs) using advanced AI content platforms.
  • Synthesize and translate complex scientific data into clear, accessible documentation for diverse stakeholders.
  • Execute comprehensive literature reviews employing AI-enhanced research methodologies.
  • Manage end-to-end publication development while ensuring compliance with international standards.
  • Drive cross-functional collaboration with medical affairs, clinical research, and AI development teams.
  • Validate and optimize AI-generated medical content while maintaining scientific accuracy.
  • Guide publication strategy and knowledge dissemination initiatives.

Artificial Intelligence

Posted 4 days ago
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πŸ“ US

πŸ’Έ 221600.0 - 277000.0 USD per year

πŸ” Oncology

🏒 Company: NateraπŸ‘₯ 1001-5000πŸ’° $250,000,000 Post-IPO Equity over 1 year agoπŸ«‚ Last layoff almost 2 years agoWomen'sBiotechnologyMedicalGeneticsHealth Diagnostics

  • M.D. or D.O. degree with board certification in Oncology.
  • At least 5 years of experience in oncology, with a background in clinical research and development.
  • Clinical experience and strong knowledge in lung cancer and immunotherapy.
  • At least 3 years of clinical trial experience in academia, biotech industry, or equivalent preferred.
  • Effective written and oral communication skills.
  • Proven skill and experience in building and managing a team.
  • Strong knowledge of clinical trial methodology, protocol development, regulatory and compliance requirements.

  • Collaborate with the Chief Medical Officer and other Medical Directors in Oncology on the clinical development of ctDNA-based diagnostics.
  • Lead development and implementation of clinical strategies for Natera's oncology products, focusing on lung cancer and immunotherapy.
  • Oversee medical education and scientific communication for healthcare providers on Natera's oncology offerings.
  • Partner with the commercial team to deliver compelling medical messages.
  • Represent Natera at medical conferences and industry events.
  • Foster a culture of scientific excellence within the oncology team.
  • Collaborate with research teams on clinical trial design and data analysis.

LeadershipProject Management

Posted 6 days ago
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πŸ’Έ 221600.0 - 277000.0 USD per year

πŸ” Oncology

🏒 Company: NateraπŸ‘₯ 1001-5000πŸ’° $250,000,000 Post-IPO Equity over 1 year agoπŸ«‚ Last layoff almost 2 years agoWomen'sBiotechnologyMedicalGeneticsHealth Diagnostics

  • M.D. or D.O. degree with board certification in Oncology is required.
  • At least 5 years of experience in oncology is required, with preference for clinical research and development background.
  • Clinical experience and strong knowledge in GU cancer is preferred.
  • Associate/full Medical Director designation based on experience.

  • Collaborate with the Chief Medical Officer and other Medical Directors on ctDNA-based diagnostic development.
  • Lead clinical strategy development for oncology products, focusing specifically on GU cancers.
  • Oversee medical education and communication for healthcare providers regarding oncology offerings.
  • Partner with the commercial team to create and deliver medical messages for oncology products.
  • Represent Natera at medical conferences and industry events, fostering a culture of scientific excellence.
Posted 6 days ago
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πŸ“ US

🧭 Full-Time

πŸ’Έ 221600.0 - 277000.0 USD per year

πŸ” Oncology, genetic testing and diagnostics

🏒 Company: NateraπŸ‘₯ 1001-5000πŸ’° $250,000,000 Post-IPO Equity over 1 year agoπŸ«‚ Last layoff almost 2 years agoWomen'sBiotechnologyMedicalGeneticsHealth Diagnostics

  • M.D. or D.O. degree with board certification in Hematology/Oncology.
  • At least 5 years of experience in oncology with a background in clinical research preferred.
  • Clinical experience and strong knowledge related to solid tumors management.
  • Ability to quickly learn Natera’s technology and its competitors.
  • Effective written and oral communication skills.

  • Collaborate with the Chief Medical Officer and other Medical Directors on clinical development of ctDNA-based diagnostics.
  • Lead development and implementation of clinical strategies for oncology products.
  • Oversee medical education and scientific communication for healthcare providers.
  • Partner with the commercial team to develop and deliver medical messages.
  • Represent Natera at medical conferences and industry events.
  • Collaborate with research teams on clinical trial design and data analysis.

Project Management

Posted 6 days ago
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πŸ“ United Kingdom

🧭 Full-Time

πŸ” Pharmaceutical, biotech, and medical device technologies

🏒 Company: global

  • Advanced degree in clinical, life sciences, or related scientific discipline preferred.
  • 2–3 years practical experience in a relevant market access or medical writing role, ideally within an agency or consulting setting.
  • Excellent verbal and written communication skills, with a professional attitude towards colleagues and clients.
  • High attention to detail, with experience in fact-checking and copy-editing.
  • Passion for writing and ability to quickly adapt to new topics.
  • Familiarity with presenting complex scientific literature and clinical trial data accurately.
  • Strong project management skills, capable of organizing and prioritizing multiple tasks in a fast-paced environment.
  • Knowledge of the pharmaceutical industry, global market access, and health technology assessments.
  • Proficiency with Microsoft Office Suite and related software.

  • Work as the primary medical writer or reviewer for developing accurate content for global value dossiers and related market access deliverables.
  • Act as the day-to-day point of contact for clients, overseeing project calls and managing project financials to keep track of scope and timelines.
  • Conduct targeted literature searches to inform project work across various disease areas.
  • Build and maintain client relationships, identifying opportunities for further projects.
  • Collaborate within the team and adapt to feedback to meet project expectations.
  • Manage workload to deliver projects on-time and on-budget while ensuring high-quality standards.
  • Contribute to internal initiatives related to content marketing and thought leadership.

Project ManagementData AnalysisClient relationship management

Posted 6 days ago
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πŸ“ United Kingdom

🧭 Full-Time

πŸ” Pharmaceutical, biotech, and medical technologies

🏒 Company: global

  • Advanced degree in clinical, life sciences or related discipline preferred.
  • 2–3 years practical experience in a relevant market access or medical writing role.
  • Excellent verbal and written communication skills.
  • High attention to detail with experience in fact-checking and copy-editing.
  • Knowledge of the pharmaceutical industry, global market access, and health technology assessments.

  • Working as the primary medical writer or reviewer to develop accurate, referenced content for GVDs and other payer-focused market access communication deliverables.
  • Acting as the day-to-day point of contact for clients, managing project calls, timelines, budgets, and scope.
  • Conducting targeted literature searches to gather relevant source materials.
  • Building client relationships and identifying opportunities for follow-on work.
  • Collaborating within a team environment and managing workload to ensure timely project delivery.

Project ManagementData AnalysisMicrosoft Office SuiteWritingClient relationship management

Posted 6 days ago
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πŸ“ United Kingdom

🧭 Full-Time

πŸ” Pharmaceutical and biotech

🏒 Company: global

  • Preferred advanced degree in clinical or life sciences; minimum Master's degree with at least 2 years of related experience.
  • Excellent verbal and written communication skills, fostering a respectful work environment.
  • High attention to detail and experience with fact-checking and editing.
  • Knowledge of presenting clinical literature and health economics in a clear manner.
  • Strong project management skills, capable of multitasking in a fast-paced environment.
  • Familiarity with pharmaceutical industry practices and health technology assessments.
  • Proficiency in Microsoft Office Suite and related software.

  • Serve as primary medical writer or reviewer for global value dossiers and other market access deliverables.
  • Act as day-to-day client contact, coordinating project calls and tracking financials.
  • Conduct literature searches to source relevant materials across various disease areas.
  • Build and maintain client relationships and seek opportunities for follow-on work.
  • Collaborate with team members and adhere to quality standards for project delivery.
  • Contribute to internal initiatives related to technology solutions and content marketing.

Project ManagementData AnalysisCommunication SkillsClient relationship managementBudgetingEditing

Posted 6 days ago
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πŸ“ United Kingdom

🧭 Full-Time

πŸ” Pharmaceutical and biotech

🏒 Company: global

  • Advanced degree in clinical, life sciences or related discipline preferred.
  • 2–3 years of practical experience in market access or medical writing role.
  • Excellent verbal and written communication skills.
  • High attention to detail with experience in fact-checking and copy-editing.
  • Strong project management skills and knowledge of health technology assessments.

  • Work as the primary medical writer or reviewer to develop accurate content for global value dossiers and other deliverables.
  • Act as the primary point of contact for clients, leading project calls and managing project financials.
  • Conduct targeted literature searches across various disease areas.
  • Build client relationships and contribute to proposals and budgets for follow-on work.
  • Collaborate within a team, incorporate feedback, and manage workload to meet project expectations.

Project ManagementData AnalysisAnalytical SkillsClient relationship management

Posted 6 days ago
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