Job description
Join Lumina Biomed, a premier leader in specialized medicine, focused on genomics and rare diseases. We are seeking a Clinical Specialist to partner with physicians, researchers, and patient communities to advance diagnostics, treatment pathways, and outcomes for complex conditions.
In this high-impact role, you will bridge clinical practice and science, translating cutting-edge genomic findings into actionable care plans, and supporting trials, regulatory submissions, and patient education. You will thrive in a collaborative, fast-paced environment that values integrity, scientific rigor, and compassionate care.
Responsibility
- Provide expert clinical guidance on genomic testing, targeted therapies, and rare disease care pathways to physicians and care teams.
- Collaborate with R&D and clinical operations to design and implement patient-centric programs, trials, and real-world evidence studies.
- Deliver technical training and education sessions for clinicians, nurses, and genetic counselors on specialized medicine offerings.
- Interpret diagnostic test results and communicate complex information with empathy and accuracy to diverse audiences.
- Support regulatory and compliance activities, documentation, and quality assurance for new diagnostics and therapies.
- Develop and maintain physician-facing materials, case studies, and patient education resources.
- Act as a regional ambassador, representing the company at conferences and professional societies.
Qualification
- Master’s or Doctoral degree in medicine, genetics, molecular biology, or a related field.
- Board-certified or eligible in relevant specialty; clinical certification in genomics/rare diseases preferred.
- 5+ years of clinical experience in specialized medicine, genomics, or rare disease management.
- Proven track record in cross-functional collaboration, research, or clinical trial support.
- Strong communication and medical writing skills; ability to translate complex data for diverse audiences.
- Experience with regulatory compliance (FDA/EMA) and medical device or diagnostic submissions is a plus.
- Proficiency with data analysis tools and EHR systems; comfort with patient advocacy and education.