
Director – Clinical Development
Oruka Therapeutics
full-time
Posted on:
Location Type: Hybrid
Location: California • Massachusetts • United States
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Salary
💰 $255,000 - $343,000 per year
Job Level
Tech Stack
About the role
- Supports the development of clinical trial protocols, including patient selection criteria, study endpoints, and data collection methods
- Oversees the conduct of clinical trials at study sites, ensuring adherence to protocols and good clinical practice (GCP) guidelines
- Reviews and interprets clinical data to assess the safety and efficacy of the investigational drug
- Authors and contributes to clinical and non-clinical documents required during the clinical development process
- Provides medical expertise of the therapeutic area, disease state, and potential drug effects
- Reviews clinical data to identify and analyze safety concerns and adverse events, and makes appropriate recommendations to the team
- Works closely with other functions including clinical operations, regulatory affairs, medical affairs, biometrics, pre-clinical and project management teams to help ensure optimization of the clinical development process
- Contributes to the overall clinical development strategy
Requirements
- Medical degree (MD) with board certification in a relevant specialty
- Extensive experience in clinical research and development, ideally within the pharmaceutical industry
- Strong understanding of clinical trial design, GCP guidelines, and regulatory requirements
- Excellent communication, leadership, and analytical skills
Benefits
- A chance to be part of a vibrant startup culture where your work can directly impact bringing new medicines to patients.
- Competitive salary and benefits package.
- A supportive and inclusive team environment where everyone is encouraged to bring their authentic selves to work.
- Opportunities for professional growth and development.
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trial protocolsdata collection methodsclinical data interpretationclinical development processsafety assessmentefficacy assessmentadverse event analysisclinical trial designGCP guidelinesregulatory requirements
Soft Skills
communicationleadershipanalytical skills
Certifications
medical degree (MD)board certification