Regional Clinical Quality Associate Director - São Paulo/Brazil

AstraZeneca plc; Cotia; Sur place; BRL 300 000 - 550 000; Plein temps

Résumé du poste

AstraZeneca in Brazil is seeking a Regional Clinical Quality Associate Director to guide quality and compliance for Oncology trials across countries supported by FSPs. You will ensure GCP adherence, lead quality oversight, and enable site management and CRO partners to deliver reliable evidence in trials.

You will build regional and country quality plans, monitor metrics, and drive proactive risk management while collaborating with global and local teams to sustain inspection readiness and

Qualifications

• Undergraduate degree in life sciences or related discipline.
• Fluent in English and Portuguese; Spanish is desirable.

Responsabilités

• Serve as primary quality and compliance contact for FSP-supported sites and CROs in Oncology.
• Develop regional and country quality plans and oversee the regional quality control plan.
• Track quality metrics, detect trends, and drive corrective actions.
• Provide regulatory and SOP expertise to regional and country teams.
• Maintain ongoing stakeholder communication to surface risks and coordinate mitigations.
• Assess training gaps and support onboarding and process updates.
• Foster a culture of quality and continuous improvement.
• Support inspection readiness and participate in audits.
• Lead governance meetings and manage risk registers and mitigations.
• Collaborate with regional quality leadership to harmonize processes.
• Participate in leadership forums and promote knowledge sharing.
• Embed lessons learned to lift regional standards.

Connaissances

Life sciences

English

Portuguese

GxP knowledge

GCP knowledge

Regulatory understanding

Risk management

Cross-functional collaboration

Study management

Analytical thinking

Communication skills

Formation

Bachelor's in life sciences

Advanced degree preferred

Description du poste

Are you ready to raise the bar on clinical quality across a high-impact Oncology portfolio and see your decisions translate into reliable studies and better outcomes for patients? Do you thrive at the intersection of regional strategy, country-level execution, and hands-on collaboration with FSP partners?

As Regional Clinical Quality Associate Director, you will be the first line of guidance on quality and compliance for countries supported by our functional service providers. You will connect regional insight with country action—building metrics-driven oversight, sharpening risk intelligence, and ensuring our studies are inspection-ready. Your work will empower site management and monitoring teams and our CRO partners to apply GCP principles confidently and consistently, so that every trial delivers dependable evidence when it matters most.

Accountabilities

• First-line Quality Leadership: Serve as the primary point of contact on quality and compliance for FSP-supported Site Management and Monitoring in Oncology and our CRO partners; provide clear direction on applying GCP and AstraZeneca standards so trials are robust and inspection-ready.
• Regional Quality Strategy: Develop regional and country quality plans and manage the annual regional quality control plan, embedding a proactive, risk-based focus on quality across assigned countries. Included is ensuring change management principles and documentation is completed as required for all SMM operational activities that qualify.
• Metrics and Risk Intelligence: Develop, track, and analyze quality metrics at regional and country level; identify trends early, anticipate deviations, and drive timely corrective and preventive actions.
• Regulatory and SOP Expertise: Investigate and consult on local regulatory guidance; apply expert knowledge of global standards and SOPs to deliver actionable compliance advice to regional and country teams.
• Stakeholder Partnership: Maintain continuous exchange with regional SMM, and country study teams to surface risks, calibrate oversight, and coordinate mitigations.
• Training and Capability Building: Assess training gaps, facilitate and support onboarding and targeted learning; collaborate on communication of global process updates promptly to secure adoption and consistency.
• Culture and Continuous Improvement: Foster an engaging quality culture; recommend and implement practical compliance improvements; amplify cross-learning from audits, inspections, and quality reviews.
• Inspection and Audit Readiness: Consult during RIST activities, inspections, and audits; coordinate internal audits where appropriate.
• Governance and Risk Management: Lead or support quality review meetings; facilitate regional and country risk registers; manage risk plans, elevate issues appropriately, and ensure mitigations are executed and tracked.
• Cross-Functional Quality Network: Collaborate closely with the regional Quality directors and broader quality community to synchronize trends, issues, and solutions across countries and processes.
• Leadership Engagement: Participate in SMM leadership meetings; enable consistent, high-quality oversight across the portfolio and drive shared accountability.
• Knowledge Sharing: Seek feedback from leadership and clinical operations, promote knowledge exchange, and embed lessons learned to lift standards across regions.

Essential Skills/Experience

• Undergraduate degree in life sciences or an equivalent related discipline.
• Fluent in English and Portuguese.
• Advance in Spanish is desirable.
• In-depth knowledge and broad experience within the pharmaceutical (biopharma) industry in a GxP regulated environment.
• Excellent communication skills with a proven ability to effectively network cross functionally and globally.
• Critical thinking, influencing and communication skills.
• Ability to collaborate, network and interact widely and effectively at all levels.
• Strong risk-based decision-making skills.
• Excellent understanding of the drug development process and related GXP activities
• Excellent understanding of the skills and knowledge required for the successful delivery of a clinical study, e.g., ICH-GCP, study management.
• Excellent knowledge of international regulations and guidelines, as well as AZ Procedural Framework
• Good analytical, problem solving, negotiation and conflict resolution skills. Ability to multi-task.
• Demonstrated ability to set and manage priorities, performance targets and project initiatives in a global environment.
• Ability to collaborate proactively, deal with ambiguity, ability to build strong customer relationships and strategic working partnerships to operate across multiple domains enabling process and system harmonization and standardization.

Desirable Skills/Experience

• Advanced degree in life sciences or an equivalent related discipline.
• Experience working with global and remote cross functional teams.
• Ability to work in an environment of remote collaborators.
• Training experience for site management and monitoring staff, or related disciplines.
• Expert reputation within the business and industry.
• Good cultural awareness.

This is where science leads and curiosity has room to move. You will work within a bold Oncology pipeline backed by significant investment, with the freedom to question, explore, and turn insights into better ways of running trials. Picture unexpected teams in the same room—clinicians, data experts, technologists, and quality leaders—sparking ideas that speed promising medicines to people who need them. We unite academic collaborators and industry partners to solve some of the toughest cancer challenges, and we value kindness alongside ambition so that smart risk‑taking is paired with real support. Your quality leadership will help transform cutting‑edge research into treatments that change lives.

Date Posted

20-ago.-2026

Closing Date

30-ago.-2026

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry‑leading skills. We believe that the more inclusive we are, the better our work. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non‑discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.