Job description
Join NexusBio Therapeutics, a leader in translational medicine focused on rare and complex diseases. We are seeking a Senior Medical Scientist to lead end-to-end research programs in Specialized Medicine, bridging clinical insight with cutting-edge science to deliver patient-centered therapies. This role blends scientific strategy, cross-functional collaboration, and hands-on execution in a fast-paced environment.
As a key member of our Medical Affairs and R&D teams, you will design clinical concepts, oversee study design, contribute to regulatory submissions, and communicate data-driven insights to internal and external stakeholders. The ideal candidate has a track record in translational medicine, a passion for patient impact, and the ability to translate complex data into compelling narrative for scientific and medical audiences.
Responsibility
- Lead translational research programs in Specialized Medicine, from target prioritization to data-driven decision making.
- Design and oversee clinical study concepts, endpoints, and statistical analysis plans in collaboration with biostatistics and clinical operations.
- Partner with Regulatory, Medical Affairs, and R&D to prepare scientific submissions and publications.
- Develop and communicate strategic medical plans that align with corporate objectives and patient needs.
- Mentor scientists and coordinate cross-functional teams across projects and phases.
- Analyze and interpret complex genomic, proteomic, and biomarker data to inform program direction.
- Represent the company at scientific conferences and with external collaborators to advance partnerships.
- Ensure compliance with ethical standards, GxP, and regulatory guidelines across all programs.
Qualification
- Advanced degree (PhD, MD, or PharmD) in medicine, biology, pharmacology, or a related field.
- Minimum 5-7 years in translational medicine, clinical development, or Medical Affairs within the biotech/pharma sector.
- Proven track record designing and executing translational studies and interpreting complex data.
- Strong understanding of regulatory requirements for rare disease/innovative therapies (FDA/EMA).
- Excellent scientific communication skills, with publications and presentations.
- Experience leading cross-functional teams and project management.
- Proficiency in bioinformatics, biostatistics, and data visualization tools.
- Ability to work independently in a fast-paced environment and influence stakeholders.