Location: Barcelona Spain (Hybrid Model)
This role requires working from the office 03 days per week.
This position is responsible for the timely preparation of high-quality regulatory-compliant nonclinical and clinical documents in support of the clinical development portfolio at the Alexion Rare Disease Unit (Alexion). The role supports medical writing activities across multiple therapeutic areas modalities and disease indications for early-stage clinical programs and contributes to late-stage programs through the authoring of nonclinical and clinical pharmacology regulatory documents. The position operates with moderate supervision.
In support of Alexions mission to improve the lives of people affected by rare diseases the Medical Writing & Clinical Trial Transparency (MW&CTT) team leads the development of strategic high-quality and compliant documents to enable clinical research and regulatory approval of new therapies while ensuring ongoing compliance with applicable laws policies regulations and public commitments related to transparency and disclosure.
The Alexion Medical Writing team provides expert leadership and strategic authorship of clinical and nonclinical regulatory documents and supports Alexions core therapeutic areas across all phases of clinical development.
Responsabilities:
Support clinical program teams by authoring and managing the development and completion of high-quality clinical regulatory documents including but not limited to early-stage clinical study protocols and amendments clinical study reports Investigators Brochures and other IND/CTA or global regulatory submission documents.
Author documents ensuring that relevant regulatory technical and quality standards are achieved and that relevant processes and best practices are applied.
Balance multiple tasks in parallel potentially across several drug projects and deliver on priorities.
Ensure strategic organization clarity accuracy format and consistency of scientific content.
Proactively collaborate with other functions including as needed with external service providers/contractors.
Develop effective collaborations with other functional lines within Alexion and keep abreast of regulatory industry and MW knowledge and best practice.
Strive for continuous improvement and operational excellence from a communications leadership perspective including representing Alexion MW.
Work independently but with the guidance and support of more senior members of the group.
This is an individual contributor position with no direct reports.
Essential Skills/Requeriments:
Education or experience in science preferably pharmacology (PhD not required but preferred)
Academic foundation in science preferably pharmacology
Strong understanding of pharmacology data sets able to quickly analyze and summarize for submission documents.
Experience in regulatory documentation and/or medical communications.
Medical Writing experience in the pharmaceutical industry.
Excellent oral written and presentation skills.
Knowledge of the technical and regulatory requirements related to the role.
When we put unexpected teams in the same room we unleash bold thinking with the power to inspire life-changing -person working gives us the platform we need to connect work at pace and challenge perceptions. Thats why we work on average a minimum of three days per week from the office. But that doesnt mean were not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
At AstraZenecas Alexion division youll find a place where innovation meets purpose. Our commitment to rare diseases means your work directly impacts lives. With a rapidly expanding portfolio and an entrepreneurial spirit akin to a leading biotech youll thrive in a culture that values connection and exploration. Supported by exceptional leaders and peers youll be empowered to grow your career while making a difference where it truly counts.
Ready to make an impact Apply now to join our team!
Date Posted
22-dic-2025Closing Date
25-ene-2026Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness. The Company will not make decisions about employment training compensation promotion and other terms and conditions of employment based on race color religion creed or lackthereof sex sexualorientation age ancestry national origin ethnicity citizenship status marital statuspregnancy (including childbirth breastfeeding or related medical conditions) parental status (including adoption or surrogacy) military status protected veteran status disability medical condition gender identity or expression genetic information mental illness or other characteristics protected by law. Alexion provides reasonable accommodations to meet the needs of candidates and employees. To begin aninteractive dialogue with Alexion regarding an accommodation please contact . Alexion participates in E-Verify.
Required Experience:
Senior Manager
AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, ... View more