משרה 4056 | דרוש עובד/ת בתחום אחיות בכל הארץ

דרוש עובד/ת בתחום אחיות בכל הארץ

כל הארץ ₪בראיון

משרה מלאה 2026-06-07 00:11:24

פרטי המשרה

We are seeking a dynamic and experienced Medical Director (MD), responsible for leading all clinical research and development activities, representing the company to external stakeholders and leading the monitoring, evaluation, and reporting of adverse events (AEs). This role combines scientific and clinical leadership with strong public-facing capabilities. The position requires proven experience in designing and executing clinical trials, authoring clinical documentation, and confidently presenting the company’s science and products to investors, media, and global partners. Key Responsibilities Clinical Trial Leadership Lead the full lifecycle of clinical trials: planning, protocol development, execution, monitoring, and final reporting. Design and write study protocols, investigator brochures, and clinical study reports. Define product indications, endpoints, and success criteria in collaboration with cross-functional teams. Ensure alignment with GCP, regulatory requirements, and business goals Medical Strategy and Scientific Oversight Translate scientific data into strategic clinical positioning/ Provide ongoing medical guidance to R&D and product teams. Support post-market clinical evaluations and medical risk assessments/ Regulatory and Documentation Lead medical writing for regulatory submissions and clinical documentation. Collaborate closely with QA/RA to ensure full compliance with global health authorities/ Contribute to IP generation through clinical validation External Representation and Communication Serve as the company's medical spokesperson to investors, media, conferences, and professional forums Present complex medical data in a compelling and accessible manner to various audiences. Act as a thought leader in the plant-based therapeutic and nutraceutical domains Medical Risk and Adverse Event Management events (AEs) related to products, in alignment with internal safety procedures and applicable regulatory requirements. Act as the medical point of contact for serious or escalated product-related complaints. Required Qualifications MD degree – mandatory 8–10 years of experience in clinical research and/or medical affairs within biotech/pharma/supplement industries. Strong track record in leading clinical trials (phases I–IV) and medical documentation. Experience authoring protocols, IBs, CSRs, and submissions to IRBs or regulatory bodies. Excellent presentation, storytelling, and public speaking skills. High level communication and interpersonal skills, a team player. Fluent in English and Hebrew (written and verbal). Willingness to travel internationally on occasion. * משרה מס׳ #728416 מיועדת לגברים ונשים כאחד.