Medical Writer
Biorce
About the company Biorce is a pioneering Healthtech company dedicated to revolutionizing drug development through the power of AI. We are passionate about accelerating medical advancements and improving patient outcomes. Our team comprises seasoned clinical research professionals, data scientists, and AI experts, working collaboratively to bridge the gap between cutting-edge technology and real-world clinical needs. With an unwavering commitment to revolutionize healthcare, we envision a world where all patients benefit from accelerated and cost-effective access to treatments. Biorce is poised to redefine the landscape of healthcare, shaping a future where innovation and accessibility converge for the betterment of humanity. About the role As Medical Director, you will be the senior medical authority for Aika, responsible for clinical integrity, medical governance, and therapeutic strategy. You will ensure that the platform’s recommendations and workflows are grounded in sound medical science, patient‑centric design, and best practices in clinical development. Key responsibilities Provide medical oversight and sign‑off for Aika’s core clinical functionalities, including protocol design support, eligibility logic, and endpoint frameworks. Shape the medical and therapeutic strategy of the platform, prioritizing features and capabilities that address real‑world challenges in drug and device development. Lead medical input into product requirements, ensuring that AI models and workflows reflect current standards of care, clinical guidelines, and regulatory considerations. Partner with Clinical, Product, and Commercial teams to engage with key opinion leaders, sponsors, and investigators, gathering insights to refine and expand Aika’s medical value proposition. Oversee the development of medically robust case studies, value narratives, and evidence dossiers for clients Act as a key spokesperson for Biorce on medical and clinical topics, including participation in advisory boards, scientific conferences, and strategic partner discussions. Support the preparation of peer‑reviewed publications and thought‑leadership pieces that highlight the medical impact and safety‑conscious design of Aika. Profile: Medical degree or equivalent, with significant experience in clinical development, medical affairs, or related functions in pharma, biotech Deep understanding of clinical trial methodology, endpoint selection, and benefit‑risk assessment, ideally with exposure to multiple indications or therapeutic areas Experience working with or overseeing digital health is highly desirable Strong stakeholder management skills High level of integrity and accountability and scientific communication Why Join Us? A dynamic work environment with an international team, where collaboration and diversity thrive. Work alongside top talent, united by a shared purpose and committed to making a real impact. Comprehensive private health coverage to ensure your physical and mental well‑being. Company-sponsored gym membership to support your fitness goals. Hybrid work model offering flexibility to balance your professional and personal life. Pet-friendly office with stunning ocean views. Coffee, tea, beverages, and snacks to keep you fueled throughout the day. Company events to celebrate achievements and enjoy time together. Get equipped with a MacBook to enhance your productivity and work experience. #J-18808-Ljbffr
$30 - $35 per hour
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