Leger Uten Grenser
Join Our Emergency Response Team We are continuously seeking qualified medical and non-medical personnel ready to deploy their expertise where it's needed most. Our mission requires maintaining predictable staffing capacity to respond swiftly when emergency medical assistance is critical. About Emergency Response Work When acute crises occur, we depend entirely on qualified, experienced personnel who can deploy at short notice. For safety reasons—yours, your colleagues', and our patients'—we do not deploy first-time personnel to disaster areas without thorough preparation and training. Our Recruitment Approach We maintain continuous recruitment to build our response capacity. Through various assignments, you'll develop expertise and readiness for when disaster response staffing is needed. This progressive approach ensures both safety and effectiveness in the field. Application Requirements Language: All applications and documents must be submitted in English Authentic Responses: Please answer application questions without AI assistance—we want to understand your personal motivation and experience from your perspective Documentation: Resume and supporting documents in English Preparation Resources Before applying, we encourage you to: Review our organizational charter and mission Explore detailed information about field work opportunities Learn about specific medical and non-medical project needs Understand our ethical guidelines and behavioral commitments Attend an information meeting about field work (if available) Ready to Make a Difference? If you're committed to providing emergency medical assistance to those who need it most and are prepared for the demands of international humanitarian work, we want to hear from you. Your expertise could be crucial in our next emergency response.
Michael Marshall Design Architecture
Project Coordinator Location: Muscat, Oman We are seeking an experienced Project Coordinator to support the delivery of hospital projects in Muscat, Oman. The role is design-focused and coordination-driven, working closely with experienced design teams, local consultants, and government stakeholders. This position is ideal for an Architect or Engineer with strong healthcare project exposure who thrives in fast-paced, multi-disciplinary environments. Key Responsibilities Coordinate day-to-day activities related to hospital and healthcare design projects Act as a local coordination point between international design teams, consultants, and client representatives Support design meetings, workshops, and technical discussions Track design submissions, comments, and responses across disciplines Assist in managing project documentation, schedules, and correspondence Support authority coordination and stakeholder engagement during the design phases Prepare meeting minutes, follow-up actions, and progress updates Ensure alignment between architectural, engineering, and medical planning teams Minimum Requirements Minimum 5 years of professional experience Background as an Architect or Engineer Proven experience in hospital/healthcare design projects Strong understanding of design coordination and multidisciplinary workflows Ability to communicate clearly with consultants, clients, and authorities Experience working on projects in Oman or the GCC is a strong advantage Proficient in MS Office; familiarity with BIM/Revit is a plus Strong organizational and coordination skills Professional level English (Arabic is an advantage) What We Offer Involvement in major healthcare projects in Oman Stable and professional working environment Clear role definition focused on design coordination Competitive package aligned with local market experience Opportunity for long-term engagement based on performance Job Type: Full-time
Guardant Health
Guardant Health - Country Medical Lead, Medical Affairs (Italy) Company Overview Guardant Health is a leading precision oncology company focused on helping conquer cancer globally through proprietary tests, vast data sets and advanced analytics. The Guardant Health oncology platform leverages capabilities to drive commercial adoption, improve patient clinical outcomes and lower healthcare costs across all stages of the cancer care continuum. Guardant Health has commercially launched Guardant360®, Guardant360 CDx, Guardant360 TissueNext™, Guardant360 Response™, and GuardantOMNI® tests for advanced stage cancer patients, and Guardant Reveal™ for early-stage cancer patients. The Guardant Health screening portfolio, including the Shield™ test, aims to address the needs of individuals eligible for cancer screening. About the Role Based in Italy, the Country Medical Lead, Medical Affairs will educate and develop academic key opinion leaders (KOL) champions with current study findings supporting the clinical value of Guardant Health's products. This role will co-develop studies and publication strategies to achieve positive guidelines, physician adoption, and support private and public payer coverage. The position reports to the Medical Affairs Director South of Europe. This role focuses on abstract and publication creation, developing physician educational materials, and training speakers for academic events, advisory boards, and CME lectures. The successful candidate will build strategic partnerships with leading cancer centers throughout Italy and community-based oncology groups, translating research data into actionable insights through publications and presentations. Key Responsibilities Identify clinical unmet needs in diagnostic and therapeutic pathways with healthcare professionals, patients and payers Develop and maintain collaborative relationships with premier cancer center KOL champions Partner with Sales executives to identify strategic healthcare partnerships including evidence generation opportunities Drive development of clinical utility projects and investigator-initiated studies for market access Create and review educational slides based on new publications and research findings Lead speaker programs and education for clinicians with expertise in solid tumors Prepare on-site presentations, data reviews, and interactive education events for KOLs Assist in Clinical Advisory Board planning and meeting facilitation Draft study protocols, publication plans, abstracts and publications with external KOL coauthors Lead Medical Science Liaison and Clinical Oncology Specialist teams nationally Support market access activities and development of payer adoption materials Collaborate with clinical trial managers on ongoing trials and data generation Identify and organize presence at major scientific conferences Plan yearly budget requirements to achieve Medical Affairs country goals Required Qualifications Education & Experience: Terminal degree in scientific field (Pharm.D., Ph.D., M.D. or Master's with academic equivalent) Clinical expertise in Oncology highly desirable Minimum 3-5 years healthcare experience in pharmaceutical, biotech, academic or cancer diagnostic industry 8+ years experience in biotechnology, diagnostics and pharmaceutical industry with oncology focus Technical Skills: Advanced knowledge of biotechnology, diagnostics and pharmaceutical industry Experience with academic medical centers building consensus around new products Proven team building and management capabilities Successful publication record as primary author of peer-reviewed publications Track record of presentations at academic centers resulting in product adoption Experience in study protocol design and documentation Prior experience as Medical Affairs professional in novel clinical product introduction preferred Core Competencies: Proficiency in Microsoft Office (PowerPoint, Excel, Word) Ability to work independently and remotely while maintaining teamwork ethic Multi-dimensional abilities to handle simultaneous tasks across teams and organizational levels Self-directed, intrinsically motivated, and flexible in dynamic environment Strong problem-solving skills, attention to detail, and time management Exceptional human relations and coordination skills Outstanding oral presentation skills in Italian and English Highly developed written communication skills for technical briefs and scientific publications Excellent proofreading abilities Additional languages beyond English and Italian are advantageous Work Environment Extensive travel requirements: 3-4 days per week, approximately 40-50% of working time Primarily national travel with occasional international conferences (ASCO, ESMO) Some weekend work required for scientific conferences Home-based office with extensive computer use High-paced, high-energy environment requiring multitasking abilities Physical ability to handle extensive travel via various transportation modes Additional Information Guardant Health is committed to providing
Innovation Sprint
Internship & Academic Assignment Opportunities at Innovation Sprint We welcome students to complete their bachelor/master thesis assignments or internships with our dynamic team. If you're studying Computer Science, Biomedical Engineering, Design, or other relevant fields and seeking an exciting experience in eClinical trials, Digital Therapeutics, eHealth, or Life Sciences, explore our available positions or submit an open application. What We Offer Supervision and guidance from experts with academic backgrounds (PhDs and Masters) Integration into a multi-disciplinary and international team One-on-one introductions to cutting-edge topics including eClinical Trials, Innovation Management, and AI in healthcare Insights into startup formation, validation, and growth in the Life Sciences domain Areas of Focus Signal processing Artificial Intelligence / Machine Learning Conversational agents Graphic design / UX eHealth: persuasive technology Business Intelligence & Insights Work Arrangements We offer flexible assignment locations: Brussels (BLSI incubator) On-site in Athens, Greece or Enschede, Netherlands Remote (from anywhere) Visit our Careers page to learn about our mission, values, and team. If you're ambitious and ready to excel, we want to hear from you. ARE YOU READY TO SPRINT?