Arcus Biosciences is a rapidly growing, clinical-stage, global biopharmaceutical company developing differentiated molecules and combination medicines that may have the potential to help people with cancer live longer. Located in the San Francisco bay area, Arcus Biosciences offers a competitive compensation and benefits package, including aggressive participation in the growth of the company in the form of stock option grants. Arcus has an ambitious undertaking and expects to become a force in the discovery, development and commercialization of novel combination therapies to treat cancer in areas of high unmet need. Our employees enjoy operating in an exceptionally dynamic and team-driven environment in which the “rule book” has not yet been written.

Description

This position supports the Clinical Quality Assurance function by providing GCP compliance oversight and support to Arcus Clinical Development therapeutic areas. The key activity of the role is providing expertise and guidance regarding applicable regulatory, Good Clinical Practice, and Arcus Standard Operating Procedure requirements for the conduct of clinical studies. Primary responsibilities will include inspection readiness planning, management of health authority inspections and audits by external development partners, management of clinical audit programs, and oversight of consultant auditors. This role will lead audits of investigator sites, internal functional/process audits, and audits of clinical vendors (GCP, GCLP, GPvP).

As a GCP compliance expert, the AD/Director of Clinical Quality Assurance (Audits & Inspections) will utilize a risk-based and phase-appropriate strategy to prioritize GCP QA support for clinical functions, identify and escalate compliance issues, enable proactive decision making, and support the development and execution of effective and comprehensive action plans to address quality and compliance risks. In addition, the AD/Director of Clinical Quality Assurance will partner with clinical functional areas to develop/revise Policies, SOPs, and Work Instructions. This role will work closely with colleagues on the CQA (Study Compliance) team to support ongoing quality/compliance oversight and guidance for study management teams. This role may mentor junior members of the CQA organization as they gain auditing experience, develop their auditing skills, and work toward becoming fully qualified GCP auditors.

The AD/Director of Clinical Quality Assurance will actively contribute to the development, maintenance, and implementation of GCP-related Policies and SOPs. This role will participate in the management of systems relevant to the administration of the Clinical QMS in support of regulatory requirements for application in drug development and clinical trial execution within the Arcus Clinical Organization. This role supports investigations of quality events and provides oversight of corrective actions. This position reports to the Senior Director of Clinical Quality Assurance (Audits & Inspections).

Responsibilities:

Identify and escalate significant compliance issues to Clinical QA and other relevant leadership.
Maintain high level of expertise in global GCP regulations and internal policies and procedures that impact clinical study conduct.
Lead external GCP/GCLP/GPvP audits of clinical vendors.
Lead investigator site audits for clinical studies.
Perform internal GCP audits of clinical functions.
Manage annual audit programs to ensure compliance with Arcus auditing SOPs and Clinical Study Audit Plans.
Oversee and support GCP-related CAPAs and process deviations.
Establish relationship with CRO and development partner quality team members for the ongoing review of quality and compliance issues.
Identify and anticipate trends in quality issues and collaborate with department management to ensure risk-managed solutions are implemented in a timely fashion
Support Inspection Readiness activities and make recommendations for its continuous improvement
Support health authority inspections of Arcus, clinical vendors, and investigator sites.
Participate in quality and compliance initiatives, as assigned

Requirements:

A minimum of 8 to 10 years of experience in a GCP related discipline. Prior experience as a CRA, Study Coordinator, or in clinical study management is strongly preferred.
Expert knowledge of global GCP requirements and applicable drug development regulations, including USA (FDA), European (EMA, MHRA), and ICH Guidelines.
Knowledge of Good Pharmacovigilance Practices, or experience working in a Safety/PV role.
Knowledge of Good Clinical Laboratory Practices.
Experience leading audits of GCP/GCLP/GPvP vendors, investigator sites, and internal audits of clinical functional areas.
Experience managing inspection readiness activities and supporting FDA, EMA, and other health authority inspections.
A strong team player with great interpersonal and written communication skills
Demonstrated strength in analytical and strategic assessment of regulatory compliance risks and the ability to articulate potential business impact.
Must be flexible and comfortable with a risk-based approach to quality and ownership of quality across functional lines.
Highly self-motivated, well-organized, and confident, with a solution-oriented mindset. Able to develop innovative solutions to problems.
Ability to influence people at different levels and negotiate cross-functionally in a matrix organization to resolve conflicts.
Ability to build and sustain meaningful relationships with business stakeholders and partners.
Strong computer literacy in MS Word, Excel, Project, Visio, PowerPoint and Veeva Vault platform applications
Bachelor’s degree or higher in a medical or health sciences related field (advanced degree preferred).
Ability to travel up to approximately 30% domestic and international, as needed.

Physical Requirements: Must possess mobility to work in a standard office setting and use standard office equipment, including a computer; vision to read printed materials and a computer screen; and hearing and speech to communicate in person, before groups, and over the telephone. This is primarily a sedentary office classification although standing in work areas and walking between work areas may be required. Finger dexterity is needed to access, enter, and retrieve data using a computer keyboard, mouse, or calculator, and to operate standard office equipment. Positions in this classification occasionally bend, stoop, kneel, reach, push, and pull drawers open and closed to retrieve and file information. Employees must possess the ability to lift, carry, push, and pull materials and objects weighing up to 25 pounds.

This role can be based at our Hayward or Brisbane, CA locations or can be remote based. The anticipated salary range for fully qualified candidates applying for this position is $185,000 - $195,000 USD annually. This salary range is an estimate of what we reasonably expect to pay for this posted position. The actual salary may vary based on various factors including, without limitation, individual education, experience, tenure, skills and abilities, internal equity and alignment with market data. In addition to a competitive market-based salary, Arcus offers the opportunity to participate in stock programs, a performance-based bonus, and a comprehensive benefits package. Additional information about our total rewards program can be found here: https://arcusbio.com/careers.

Arcus Biosciences is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. Arcus is committed to the principle of equal employment opportunity for all employees and does not discriminate based on race, religion, color, sex, gender identify, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other legally protected status. EOE/AA/Vets

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AD, Clinical Quality Assurance (Audits & Inspections) (Office OR Remote)

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