Job description
Join NovaThera, a leading innovator in specialized medicine, to advance clinical programs for rare diseases and targeted therapies. We blend scientific excellence with patient-centric execution in a fast-growing biotech environment.
In this role you will collaborate with Clinical Operations, Medical Affairs, and Regulatory teams to shape study design, ensure regulatory readiness, and translate complex data into actionable insights for patients and providers.
We offer a collaborative culture, competitive compensation, and a path toward leadership in a dynamic field.
Responsibility
- Lead end-to-end planning and execution of clinical programs in specialized medicine, including rare diseases.
- Design study protocols, drive site selection, and oversee patient recruitment strategies.
- Collaborate with cross-functional teams to meet milestones and ensure regulatory readiness.
- Oversee safety monitoring, pharmacovigilance, and adverse event reporting in compliance with GCP.
- Interpret clinical data, contribute to medical writing, and support submissions to regulatory authorities.
- Represent the organization at clinical conferences and engage with external investigators and key stakeholders.
- Mentor junior team members and foster a culture of scientific rigor and patient focus.
Qualification
- MD, DO, PhD, or equivalent advanced degree in a relevant field.
- 5+ years in clinical research, translational medicine, or specialized disease areas.
- Strong knowledge of regulatory guidelines (FDA/EMA), GCP, and trial design.
- Experience with protocol development, data analysis, and medical writing.
- Excellent communication, presentation, and stakeholder management skills.
- Ability to work cross-functionally in a fast-paced biotech environment and manage multiple projects.