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Assoc Director Quality Assurance, GCP (contract)

erasca
San Diego, CA Remote Full Time
POSTED ON 4/11/2025 CLOSED ON 4/24/2025

What are the responsibilities and job description for the Assoc Director Quality Assurance, GCP (contract) position at erasca?

Erasca is a clinical-stage precision oncology company focused on discovering, developing and commercializing medicines for the benefit of patients with cancer. Our programs take novel approaches to shutting down one of cancer’s most commonly mutated signaling cascades, the RAS/MAPK pathway, which affects approximately 5.5 million lives each year worldwide. The name “Erasca” has an important embedded meaning: it is a contraction of our audacious hope to “erase cancer” that drives our mission and everything that we do on behalf of patients with cancer.

Position Summary:  

This position will be responsible for the execution and oversight of vendor audit policies, plans, and quality system elements related to GxP audit activities in support of clinical programs & studies along with external GxP qualifications and inspection readiness. In addition, the role facilitates quality contractual reviews and obligations (such as Quality Agreements), oversees supplier scorecards, performance and quality, and supports GDPR compliance and serious breach assessment. This person will sit on clinical study teams and work closely with cross-functional stakeholders in clinical operations, clinical development, data management, and other functions involved in the conduct of Erasca clinical trials. 

Note this is a part time contract position, 20 hours per week, and can be based anywhere in the United States. 

Responsibilities:  

  • Establish, maintain, and ensure effectiveness of quality programs and documentation to assure compliance in international regulatory environment and provide guidance in clinical Quality related areas.
  • Represent Quality Assurance on cross-functional study teams.
  • Support GCP QA in the conduct and oversight of GxP vendor audits (GMP, GCP, GLP, and & GVP), including IT systems.   
  • Maintain risk based GxP supplier/vendor audit schedule and performance overview in compliance with procedures. Author (or ensure authorship for outsourced audits), review, and approve internal and external audit reports.  
  • Review audit findings and other potential compliance risks to subject safety, data integrity, and business operations and escalate risks to QA management.  
  • Ensure audit reports and corrective actions are developed and completed within timelines mandated in internal procedures as well as ensuring appropriate effectiveness checks through subsequent vendor audits. 
  • Author, review, and facilitate contractual agreements (Quality Agreements, Pharmacovigilance Agreements (PVA), etc.).
  • Perform all duties in keeping with the Company’s core values, policies and all applicable regulations. 

Requirements:  

  • Undergraduate degree in in Biology, Chemistry, Physical Sciences, or related discipline, or comparable experience. 
  • 10 years of experience including management of GxP Quality/Compliance audits in a pharmaceutical or biotech environment required.
  • Extensive knowledge of ICH Guidelines, US, European, and ROW regulatory requirements regarding applicable drug development regulations.  
  • Experience with transition from Phase 1-3 to commercial quality systems preferred. 
  • Previous experience working with FDA and participating in regulatory agency inspections of clinical research activities.
  • Excellent interpersonal and influencing skills.
  • Must have good written and verbal communication skills with the ability to tailor communication to all levels and prepare and present appropriate updates to functional groups and leaders. 
  • Demonstrated ability to achieve high performance goals and meet deadlines in a fast-paced environment.
  • Strong learning orientation, curiosity, and commitment to science and patients.

Along with our casual, collaborative, and fun work and the chance to make your mark in our mission to erase cancer, Erasca offers a comprehensive and competitive benefits package that includes: Paid Time Off, Holiday, and Sick Leave, Medical, Dental and Vision Plans, Short- and Long-Term Disability, Basic and Voluntary Life/AD&D Coverage, Flexible Spending Accounts (FSA, HSA, and Commute), Critical Illness and Accident Coverage, Pet Insurance, Employee Assistance Program, 401(k) Plan with Erasca contribution, and the opportunity to participate in an Employee Stock Purchase Program. 

Erasca, Inc., is an Equal Opportunity Employer and takes pride in maintaining a diverse and inclusive environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of sex , race, religion, national origin, ancestry, physical or mental disability, protected medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military and veteran status or any other basis protected by federal, state or local law or ordinance or regulation.

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