About Company
AstraZeneca is a global, science-led biopharmaceutical company that focuses on the discovery, development, and commercialisation of prescription medicines, primarily for the treatment of diseases in oncology, rare diseases, and bio-pharmaceuticals, including cardiovascular, renal & metabolism, and respiratory & immunology. Based in the heart of the renowned Cambridge Biomedical Campus, our state-of-the-art facilities foster an environment of groundbreaking innovation, collaboration, and a relentless pursuit of scientific excellence. We are driven by a singular purpose: to push the boundaries of science to deliver life-changing medicines to patients worldwide. Joining AstraZeneca means becoming part of a diverse and inclusive team that is committed to making a tangible difference to global health. Your work here will directly contribute to advancements that could impact millions of lives, offering not just a job, but a profound sense of purpose within a world-leading scientific community.
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Job Description
Are you a skilled communicator with a passion for transforming complex scientific data into clear, compelling, and compliant medical narratives? AstraZeneca is actively seeking a talented and dedicated Medical Writer to augment our expert team in Cambridge, Cambridgeshire. In this crucial role, you will be at the forefront of crafting high-quality scientific and medical documents that are essential for the development, regulatory approval, and successful commercialisation of our innovative pharmaceutical products. You will engage in close, dynamic collaboration with an array of multidisciplinary teams, including clinical development specialists, regulatory affairs experts, biostatisticians, and medical affairs professionals, ensuring that all written materials are meticulously accurate, fully compliant with international guidelines, and strategically aligned with our overarching scientific objectives. This position provides an unparalleled opportunity to contribute significantly to the communication strategy for a diverse portfolio of groundbreaking medicines, spanning from their nascent stages in clinical trials through to critical post-marketing support activities. You will be entrusted with the development of a wide spectrum of deliverables, from clinical study reports and regulatory submissions to scientific publications and presentations, each demanding precision and clarity. If you thrive in a fast-paced, intellectually stimulating environment, possess an unwavering eye for detail, and are deeply committed to upholding scientific rigor and integrity, we strongly encourage you to apply. This role is perfectly suited for an individual eager to make a tangible and lasting impact on patient lives through expert scientific communication within a globally recognised biopharmaceutical powerhouse. At AstraZeneca, we champion a culture of continuous learning, professional development, and mutual support, providing you with the necessary tools and mentorship to advance your career alongside some of the brightest minds in the pharmaceutical industry. Your aptitude for distilling intricate scientific information into accessible and impactful content for diverse target audiences will be a cornerstone of our collective success.
Key Responsibilities
- Develop, write, edit, and review a comprehensive range of scientific and medical documents, including but not limited to clinical study reports, protocols, investigator brochures, regulatory submission documents, abstracts, manuscripts for peer-reviewed journals, and scientific presentations.
- Ensure all documentation strictly adheres to relevant regulatory guidelines (e.g., ICH-GCP, EMA, FDA), internal company Standard Operating Procedures (SOPs), and industry best practices for medical writing.
- Collaborate effectively and proactively with global study teams, therapeutic area experts, biostatisticians, and other internal and external stakeholders to gather essential information and incorporate feedback efficiently.
- Maintain an up-to-date and in-depth knowledge of assigned therapeutic areas, relevant scientific literature, and evolving regulatory requirements.
- Manage multiple concurrent projects with varying deadlines, ensuring timely delivery of high-quality, scientifically accurate, and grammatically impeccable output.
- Actively participate in scientific and strategic team meetings, providing expert input on document content, communication strategies, and scientific messaging.
Required Skills
- Exceptional written and verbal communication skills in English, with a proven ability to convey complex scientific information clearly and concisely.
- Strong understanding of medical terminology, clinical research methodologies, and the end-to-end drug development process.
- Demonstrated proficiency in critically interpreting, analysing, and presenting complex scientific and clinical data from various sources.
- Outstanding attention to detail, accuracy, and consistency in all written work.
- Ability to work both independently and as a highly collaborative team member in a dynamic, deadline-driven environment.
- Advanced proficiency with Microsoft Office Suite, particularly Word, Excel, and PowerPoint.
Preferred Qualifications
- PhD or Master's degree in a life science, medical, pharmaceutical, or related scientific discipline.
- A minimum of 3 years of progressive experience as a Medical Writer within the pharmaceutical, biotechnology, or Contract Research Organization (CRO) industry.
- Prior experience with regulatory submission documents (e.g., New Drug Applications/Biologics License Applications (NDA/BLA), Marketing Authorisation Applications (MAA)).
- Familiarity with medical writing software, publication planning tools, and content management systems.
Perks & Benefits
- Highly competitive salary package and attractive performance-based bonuses.
- Comprehensive private health, dental, and vision insurance for you and your family.
- Generous employer-contributed pension scheme and robust life assurance coverage.
- Flexible working arrangements and hybrid work options where roles permit, supporting work-life balance.
- Extensive opportunities for continuous professional development, training, and accelerated career growth within a global organisation.
- Access to state-of-the-art on-site facilities including a fitness centre, diverse restaurants, and childcare support options.
- Employee stock purchase program and other financial wellness benefits.
- Relocation assistance may be available for eligible candidates.
How to Apply
Interested candidates are invited to apply directly through AstraZeneca’s official careers portal. To begin your application, please click on the secure application link provided below. On our careers site, please search for ‘Medical Writer’ positions in Cambridge, Cambridgeshire, and submit your comprehensive CV along with a compelling cover letter. Your cover letter should articulate your relevant experience, highlight your key achievements in medical writing, and explain why you believe you are the ideal candidate to contribute to AstraZeneca’s mission. We eagerly anticipate reviewing your application and learning how your expertise can enhance our team.
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