(Senior) Clinical Quality Associate Director - 12 month secondment/fixed term contract

The Clinical Quality Associate Director (CQAD) is primarily responsible for maintaining, developing, and communicating high-quality standards in the delivery of clinical studies. This includes playing a central role in coordinating and meeting the training needs of the local Site Management & Monitoring (SMM) team through close collaboration with local SMM leadership and reporting to Director, Country Head.

This role acts as the primary advisor on compliance and process matters within the local SMM team, proactively identifying and pursuing opportunities to drive quality and process improvements at local, regional, and global levels. A key aspect of the role is the development, implementation, and continuous oversight of local procedural documents, as well as ensuring up-to-date knowledge of local regulations and industry practices pertaining to clinical trials. The CQAD supports audit and inspection activities, serving as the primary point of contact for auditors and inspectors in their local SMM organization.Working collaboratively with the local SMM leadership team, the CQAD assists in planning and executing all quality control activities and applies robust risk management principles to assess compliance issues and implement effective solutions. The CQAD stays informed about business compliance matters, working closely with the Regional Director, Clinical Quality (RDCQ), and actively engaging with key regional and global networks.This Job description applies to both senior and non-senior role levels with additional responsibilities and expectations applicable for the senior role, defined in document ‘Site Management and Monitoring (SM&M) Biopharmaceuticals Senior Role Definition’

Responsibilities

Accountabilities for this role include:

Advise Local Study Teams on AstraZeneca procedural frameworks, international guidelines such as ICHGCP, industry standards, and relevant local regulations.

Provide accurate and timely updates on local clinical trial regulations, ensuring teams are aware of any changes affecting compliance.

Support local management in planning and executing Quality Control (QC) activities as outlined in the local QC plan.

Offer expert guidance and support to local management in addressing and resolving quality-specific concerns at the local level.

Assist local teams with audit and regulatory inspection preparation, execution, and response activities, ensuring readiness and effective follow-up.

Advise Local Study Teams on resolving audit and inspection findings and assists with implementing corrective actions.

Facilitate knowledge sharing by communicating audit and inspection learnings to local staff and the regional CQAD network, as well as cascading global/regional insights on the local level.

Oversee country-level risk management, identifying and supporting mitigation actions to address compliance risks.

Serve as a key contact in the evaluation and management of fraud or misconduct cases, liaising with Quality Assurance, the Regional Director Clinical Quality (RDCQ), and local management as needed.

Identify ongoing and ad hoc training needs for local staff and coordinate or deliver training in collaboration with local SMM leadership.

Support the local implementation of global procedures and systems by providing feedback on procedural documents, delivering local training as required, and collecting and escalating user questions and issues, liaising with local subject matter expert, if applicable.

Lead or contribute to the implementation of systems and tools for delivering clinical operational tasks, SOPs, and ICH-GCP requirements at the local level.

Oversee development, maintenance, training, and archiving of Local Procedural Documents, ensuring alignment with global processes, ICH-GCP, and local regulations.

Act as the primary local interface for Quality Assurance.

Actively participate in the Clinical Quality Associate Directors’ Network at the regional level, contributing to shared goals and best practices.

Represent the organization in local regulatory or operational expert groups, as required.

Provide expert opinions on local regulations related to clinical trials when requested by other departments.

Deliver training to investigational site staff on ICH-GCP and local regulations when additional support is needed.

Requirements

Education and experience:

Bachelor’s degree in related discipline, preferably in life science, or equivalent qualification aligned to the knowledge and skills of the role and ensures successful conduct of responsibilities and appropriate interactions with internal and or external stakeholders.

Previous experience in the pharmaceutical industry, preferably in Clinical Operations/Quality Assurance.

Relevant knowledge and ability to fulfil key responsibilities, including but not limited to:

Drug development process and related GxP processes, International guidelines ICH-GCP, relevant country regulations, medical knowledge and ability to learn relevant AZ Therapeutic Areas, Clinical Study Management including monitoring, study drug handling and data management.

Personal Effectiveness & Drives Accountability in Others

Learning Agility

Financial, Technology & Process Competency

Active Listening, Fluency in written & spoken business-level English

Act with Integrity & high ethical standards

Effectively lead a team across in-person and virtual settings to deliver shared goals, demonstrates cultural awareness

Identify and champion more efficient delivery of quality clinical trials with optimised cost and time

Ability to travel nationally/internationally as required

Valid driving license, if country employment requirement

Communication & Teamwork – Influencing, Training & workshop facilitation

Effective, risk-based thinking – Problem Solving, Critical Thinking, Decision Making, Strategic Thinking,

Effective Issue Management

Clinical Study Operations (GCP) & Quality Management - Audit & Inspection Readiness, Process

Management & Improvement

Leadership – Enable Change, Feedforward & Coaching.

Date Posted

05-sie-2026

Closing Date

12-sie-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 will be.  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.