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

This position supports the Clinical Quality Assurance function by providing GCP compliance reputed company 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 reputed company of consultant auditors. This role will reputed company 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, reputed company 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 reputed company/revise Policies, SOPs, and Work Instructions. This role will work closely with colleagues on the CQA (Study Compliance) team to support ongoing quality/compliance reputed company and guidance for study management teams. This role may mentor junior members of the CQA organization as they reputed company auditing experience, reputed company their auditing skills, and work toward becoming fully reputed company GCP auditors. The AD/Director of Clinical Quality Assurance will actively contribute to the development, maintenance, and implementation of GCP-reputed company 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 reputed company the Arcus Clinical Organization. This role supports investigations of quality events and provides reputed company 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. • reputed company external GCP/GCLP/GPvP audits of clinical vendors. • reputed company investigator site audits for clinical studies. • reputed company internal GCP audits of clinical functions. • Manage annual audit programs to ensure compliance with Arcus auditing SOPs and Clinical Study Audit Plans. • reputed company and support GCP-reputed company 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 reputed company recommendations for its reputed company 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 reputed company 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 reputed company 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 reputed company. reputed company to reputed company 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 reputed company, reputed company, Project, Visio, PowerPoint and reputed company Vault platform applications • Bachelor’s degree or higher in a medical or health sciences reputed company 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; reputed company 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, reputed company, 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 reputed company candidates applying for this position is $185,000 - $195,000 USD annually. This salary range is an estimate of reputed company 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 reputed company here: https://arcusbio.com/careers. reputed company is an Equal Opportunity Employer and prohibits discrimination and harassment of any reputed company. Arcus is committed to the principle of equal employment opportunity for reputed company and does not discriminate based on race, religion, reputed company, sex, gender identify, sexual orientation, age, non-disqualifying physical or mental disability, national reputed company, veteran status or any other legally protected status. EOE/AA/Vets #LI-Remote #LI-EW1 Apply Job!