Offer summary
Qualifications:
MD, PhD, PharmD, or equivalent required, 6+ years experience in clinical research, Expertise in conducting global clinical trials, Familiarity with various clinical trial designs, Deep experience in Neuroscience/Ophthalmology or Immunology/Rheumatology preferred.
Key responsabilities:
- Develop and optimize clinical trial protocols
- Act as clinical science liaison to KOLs and PIs
- Contribute to scientific review of study documents
- Build clinical development plans and conduct assessments
- Support regulatory submissions and proposal processes