Clinical Regulatory Writing at AstraZeneca. Apply Now
Join AstraZeneca as an Associate Director – Clinical Regulatory Writing and take the lead in shaping drug development. Drive strategic regulatory communications, collaborate with cross-functional teams, and contribute to life-changing medicines. If you’re a solution-oriented leader passionate about regulatory excellence, this is your opportunity to make an impact.
Job Posting: Associate Director- Clinical Regulatory Writing
JOB TITLE: Associate Director- Clinical Regulatory Writing
CAREER LEVEL: E
Lead the way for a new breed of solutions-oriented Regulators. Champion a strategic approach to regulations, support quick decision-making, and work on shaping drug development. Be part of a team where you can follow the science and turn drug development strategies into reality.
About The Team
We are a diverse and open-minded team that accelerates discovery and development through regulatory functions. Combining knowledge from various Therapy Areas helps us deliver rapid and global approvals for introducing new medicines to patients.
About The Role
As an Associate Director, you will provide strategic leadership and communication expertise to clinical drug programs. Your responsibilities include authoring clinical regulatory documents, ensuring high-quality standards, and representing your skills in projects.
Typical Accountabilities
- Handle clinical and regulatory writing activities across a complex portfolio
- Author complex clinical-regulatory documents
- Provide strategic communications leadership to projects
- Lead submission teams and drive communication strategy
- Collaborate with internal and external teams
- Support continuous improvement and operational excellence
Requirements for Clinical Regulatory Writing at AstraZeneca
Essential:
- Life Sciences degree
- Medical writing experience in the pharmaceutical industry or CRO
- Ability to lead communication projects
- Knowledge of drug development and regulatory requirements
Desirable: Advanced degree in a scientific discipline (Ph.D.)
WHY JOIN US?
We believe in finding better ways to impact patients with serious diseases. Our advanced approach to regulation allows us to lead the field, working closely with drug development to influence and make valuable contributions throughout.
SO, WHAT’S NEXT?
If you are eager to join our team, click the following link to apply. We look forward to hearing from you!
WHERE CAN I FIND OUT MORE?
Connect with AstraZeneca on LinkedIn for updates and more information: LinkedIn
Keywords: AstraZeneca, Associate Director, Clinical Regulatory Writing, Pharmaceutical Industry, Drug Development, Communication, Medical Writing, Jobs
