Associate Director II, CReW

The role holders provide strategic leadership and communications expertise to clinical drug programs. They author clinical-regulatory documents and provide critical review to achieve high-quality standards. They represent the skill on drug and non-drug projects. The Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors strategically important clinical-regulatory documents that are label focused and align with project strategies, regulatory requirements, and communications best-practices. We support the Company’s core therapeutic areas in all phases of clinical development. Our vision is to be an industry leading organization driving critical communication excellence to achieve successful submissions and approvals.

About AstraZeneca

Associate Director II, CReW Global Career Level: E3 Role Type: Individual Contributor Work Location: Embassy Manyata Business Park About AstraZeneca AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines targeting some of the planet’s most serious diseases.

But we’re more than one of the world’s leading pharmaceutical companies.

At AstraZeneca, we 're dedicated to being a Great Place to Work.

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines.

In-person working gives us the platform we need to connect, work at pace and challenge perceptions.

We balance the expectation of being in the office while respecting individual flexibility.

Join us in our unique and ambitious world.

At AstraZeneca's Biopharmaceuticals R&D, we are part of the solution, turning our drug development strategies into reality.

We work at all stages of development to translate our life-changing science into medicines to get the best results for AstraZeneca, patients in need and healthcare professionals.

We are a diverse and open-minded team harnessing our different skills and experiences.

Our differences enable us to explore new ideas and ways of doing things.

It keeps us on our toes and excited for what's next.

Where Can I Find Out More?

Our Social Media, Follow AstraZeneca on LinkedIn https://www.linkedin.com/company/1603/ Call to Action: Step into the role that turns evidence into approvals—shape the submissions that change labels and lives, and lead the next chapter of clinical communication excellence!

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 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.

Responsibilities

• Portfolio Leadership: Independently manage clinical regulatory writing across a complex portfolio, prioritizing impact and ensuring delivery to time and quality.
• Serve as lead author for the most complex clinical-regulatory documents in a program, meeting all technical, regulatory, and quality standards while applying best practice and continuous improvement.
• When acting as submission lead, drive the clinical Submission Communication Strategy (cSCS), aligning cross-functional teams around clear positions and messages that anticipate regulator needs.
• As part of clinical delivery and submission teams, provide strategic communications leadership, set communication standards, and champion quality, efficiency, and consistency across programs.
• Partner closely with clinical, biostatistics, regulatory, safety, and operations teams to interpret complex data and craft concise, accurate messages that answer customer and regulator questions.
• Lead internal and external authoring teams, including vendor medical writers, to scale delivery while upholding scientific integrity and message discipline.
• Operate proactively at the program level, shaping clinical narratives across studies and indications and ensuring coherence from protocol to label.
• Support the development of Clinical Regulatory Writing Managers, sharing frameworks, feedback, and coaching to set the standard across the skill.
• Drive continuous improvement in our authoring model, tools, and ways of working, representing the writing skill in drug and non-drug projects for broader organizational benefit.

Requirements

• Life Sciences degree in an appropriate subject area.
• Minimum 10+ years of significant medical writing experience in the pharmaceutical industry or CRO.
• Ability to advise and lead communication projects.
• Understand drug development and communication process from development, launch through life cycle management.
• In depth knowledge of the technical and regulatory requirements related to the role.

Preferred

• Advanced degree in a scientific field (Ph.D.).

Benefits

• But that doesn't mean we're not flexible.

Desirable Skills/Experience

That's why we work, on average, a minimum of three days per week from the office.

Why AstraZeneca

We align with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements. Date Posted 26-Oct-2026 Closing Date 31-Oct-2026 AstraZeneca embraces diversity and equality of opportunity.

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.