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Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Lead clinical study design, execution, and data interpretation across a full development program
- Partner with Medical Directors and cross-functional teams to shape study strategy and scientific direction
- Author and review protocols, amendments, clinical study reports, and other key clinical documents
- Drive medical and safety data review to protect patient safety throughout the trial lifecycle
- Apply therapeutic-area knowledge to inform study design and risk mitigation
- Represent Clinical Sciences in scientific advisory boards, steering committees, and safety monitoring meetings
- Mentor and guide junior team members
- Ensure compliance with FDA, EMEA, ICH, and GCP standards across study activities
Requirements
What you’ll need- Bachelor's degree required
- Advanced degree (PhD/MD/PharmD/MSc) in life sciences or healthcare preferred
- 8+ years of pharmaceutical clinical drug development experience
- Experience in rare hematologic conditions and/or immunologic diseases preferred
- Demonstrated knowledge of GCP, clinical study design, and clinical research methodology
- Proven track record driving clinical trial process improvements
- Strong scientific and analytical skills
- Compliance knowledge of FDA, EMEA, ICH, and GCP standards
- Ability to work in a cross-functional matrix environment
- Must satisfy applicable right-to-work and background-check requirements
Benefits
Comp & perks- Annual bonuses or other incentive plans
- Equity awards
- Pension or retirement benefits
- 401(k) company match
- Health and wellness programs
- Fitness centers
- Medical, dental, vision, life, and disability insurance benefits
- Paid time off
- Family support benefits
- Reasonable accommodation for applicants with known disabilities or chronic illnesses
