Director, Clinical Quality Assurance

6 days ago

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201 - 500 employees

Founded 2015

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Description

• QED Therapeutics is developing targeted treatments for FGFR-driven skeletal dysplasias. • The Director, Clinical Quality Assurance will define and execute Clinical Controlled Document Management strategy. • Ideal candidate will have GCP experience in the biotech/pharmaceutical sector.

Requirements

• 2+ years of experience with Veeva administration highly preferred • Ability to build relationships and work collaboratively • Strong negotiation skills and solution-based approach • Strong team player with effective communication skills • Ability to handle multiple project issues simultaneously • Proficient verbal and written communication • Bachelor's degree in a scientific discipline or equivalent experience • Minimum of 6 years of experience in a GCP practice area preferred • Expertise with applicable GCP guidelines

Benefits

• Patient Days, hearing directly from individuals living with conditions we impact • Culture inspired by PUT PATIENTS FIRST, THINK INDEPENDENTLY, BE RADICALLY TRANSPARENT • Robust compensation & benefits package (Base, Performance Bonus, Equity, health, welfare & retirement) • Flexible PTO • Rapid career advancement for strong performers • Commitment to Diversity, Equity & Inclusion