Director, Clinical Regulatory Writing
AstraZeneca
Location: Barcelona, Spain (on-site) – 3 days working from the office and 2 days working from home.Job Description
Role holders expertly drive strategic communications excellence to achieve successful submissions and approvals. They develop innovative best practices and improvement initiatives.Typical Accountabilities
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 strategic communication excellence to achieve successful submissions and approvals.
The Clinical Regulatory Writing Director provides expert communications leadership for the most complex and business-critical clinical activities by driving strategic content development in alignment with product strategy and communications excellence.
The Clinical Regulatory Writing Director is encouraged to:
Education, Qualifications, Skills and ExperienceEssential
Desirable
Date Posted 08-nov-2024Closing DateAstraZeneca 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.
Barcelona
Sun, 10 Nov 2024 07:05:05 GMT
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