Oruka Therapeutics

Director – Clinical Development

Oruka Therapeutics

full-time

Posted on:

Location Type: Hybrid

Location: CaliforniaMassachusettsUnited States

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Salary

💰 $255,000 - $343,000 per year

Job Level

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