Director, Clinical Quality Assurance (CQA)
Benefits
Unlimited PTO
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Key Responsibilities:
- Author, maintain and implement study-specific Clinical Quality Audit Plan(s) for assigned clinical program(s).
- Represent Quality at cross-functional clinical program meetings and Clinical Study Team meetings.
- Maintain program oversight and influence proactive quality management through quality related activities.
Requirements:
- A minimum of Bachelor’s degree in STEM, and/or allied medical field.
- At least seven (7) years of pharmaceutical/biotech/medical device GCP Quality Assurance (QA).
- Strong working knowledge and interpretation of global GxP regulations.
Personal Characteristics:
- Capacity to produce high quality results across multiple projects.
- Excellent communications skills, both written and verbal.
- Strategic thinker, open-minded and flexible to adopting new ideas.
Immunovant
Immunovant, Inc. is a clinical-stage immunology company dedicated to enabling normal lives for people with autoimmune diseases. As a trailblazer in anti-FcRn technology, they are developing innovative, targeted therapies to meet the complex and variable needs of people with autoimmune diseases.