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Associate Director of Clinical Operations

Oruka TherapeuticsWaltham, Massachusetts, United States
Hybrid Full-time $182K/yr - $208K/yr

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Experience Level

Senior Level Manager

Qualifications

The Associate Director of Clinical Operations should possess a strong background in clinical trial management, with significant experience in a biotech or pharmaceutical setting. Expertise in regulatory compliance, project management, and cross-functional collaboration is essential. A proven ability to lead teams effectively, coupled with excellent communication skills, is required. Candidates should have a Master's degree in a relevant field and a minimum of 5 years of experience in clinical operations management.

About the job

Oruka Therapeutics is developing biologics designed to change the treatment landscape for chronic skin conditions such as plaque psoriasis. The company focuses on long-lasting relief for patients, aiming for outcomes like disease clearance with infrequent dosing. Their pipeline includes proprietary antibodies created by Paragon Therapeutics, targeting the underlying causes of dermatologic and inflammatory diseases. More details about their work can be found at www.orukatx.com.

Role overview

The Associate Director of Clinical Operations will manage the setup and execution of clinical trials, supporting the Director of Clinical Operations within a specific therapeutic area. This position oversees multiple studies, combining strategic planning with day-to-day operational involvement to keep clinical programs on track and within budget.

Responsibilities include handling operational details, anticipating challenges, and implementing solutions to ensure trial progress. The role requires someone who can move between leadership and hands-on work, maintaining a player/coach mindset throughout.

What you will do

  • Oversee all phases of clinical trial setup and execution across several studies
  • Support the Director of Clinical Operations in a designated therapeutic area
  • Balance strategic planning with direct, hands-on involvement in daily operations
  • Identify and resolve operational challenges to maintain study timelines and budgets

Requirements

  • Demonstrated integrity and sound judgment in clinical operations
  • Ability to shift between high-level oversight and direct involvement as needed
  • Strong commitment to study goals and a collaborative approach
  • Adaptability and resourcefulness in a biotech setting

This hybrid role is based in Waltham, Massachusetts, with an expectation of three days onsite each week. The team values learning, growth, and a positive, inclusive culture.

About Oruka Therapeutics

Oruka Therapeutics is at the forefront of developing transformative therapies for chronic skin diseases, dedicated to improving the quality of life for patients through innovative solutions and a commitment to excellence in clinical research.

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