Oruka Therapeutics logoOruka Therapeutics logo

Director of Clinical Quality Assurance

Oruka TherapeuticsWaltham, Massachusetts, United States
Remote Full-time $213K/yr - $240K/yr

Clicking Apply Now takes you to AutoApply where you can tailor your resume and apply.


Experience Level

Senior Level Manager

Qualifications

Qualifications:Advanced degree in Life Sciences or a related field. Minimum of 10 years of experience in clinical quality assurance or related fields. Strong understanding of GCP and regulatory guidelines. Proven leadership skills and ability to influence cross-functional teams. Excellent communication and interpersonal skills.

About the job

About Us:

At Oruka Therapeutics (Nasdaq: ORKA), we are pioneering innovative biologics aimed at transforming the treatment landscape for chronic skin disorders. Our mission is to empower individuals battling chronic skin conditions, such as plaque psoriasis, by providing them with the utmost freedom from their ailments, achieving significant disease clearance through infrequent dosing, potentially just once or twice yearly. Our proprietary collection of antibodies, meticulously crafted by Paragon Therapeutics, targets the fundamental mechanisms of plaque psoriasis and other dermatological and inflammatory conditions. To learn more, visit www.orukatx.com.

As we expand our core team, we are on the lookout for exceptional talent across various functional areas, individuals who seek more than just employment, but rather a chance to be part of something transformative. We value passion for making a difference and contributions to fostering an engaged, inclusive, and positive workplace culture.

Job Title: Director of Clinical Quality Assurance

Location: Remote; candidates located in the Waltham, MA area are preferred.

Role Overview:

The Director of Clinical Quality Assurance will provide strategic leadership and oversight for Oruka's clinical development initiatives, focusing primarily on Good Clinical Practice (GCP) and associated quality systems that support clinical trials. This role will establish, enhance, and oversee clinical quality processes appropriate to each phase, ensuring comprehensive supervision of clinical trial execution and vendor performance while preparing for global health authority inspections, including FDA Bioresearch Monitoring (BIMO) inspections.

This position will collaborate closely with Clinical Operations, Clinical Development, Biometrics, Pharmacovigilance, Regulatory Affairs, Medical Writing, and external service providers to ensure compliance with GCP, relevant global regulations, internal procedures, and protocol requirements throughout the clinical trial lifecycle. The Director of Clinical QA will proactively contribute quality insights, support continuous improvement initiatives, and help cultivate a quality-centric culture as the organization progresses with its pipeline.

Key Responsibilities:

  • Clinical Quality Oversight: Ensure compliance with GCP and applicable regulatory requirements for new and ongoing clinical studies.

About Oruka Therapeutics

Oruka Therapeutics is at the forefront of developing groundbreaking biologics aimed at elevating the standard of care for patients suffering from chronic skin diseases. Our innovative approach and commitment to patient freedom drive our mission.

Similar jobs

Browse all companies, explore by city & role, or SEO search pages. View directory listings: all jobs, search results, location & role pages.

Tailoring 0 resumes

We'll move completed jobs to Ready to Apply automatically.