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Gigg från: Astrazeneca AB

Are you our next Medical Writer colleague?

  • Vård & assistans


Diverse Minds. Bold Disruptors. Meaningful Impact. Are you a passionate Medical Writer with Clinical and Regulatory authoring experience? Can you envision using your expertise to impact patients' lives? Join our Medical Communications department to make a purposeful difference! Astra Zeneca is a global, innovation-driven Bio Pharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious disease. But we're more than one of the world's leading pharmaceutical companies. Embrace an environment built on lifelong learning. Never complacent, we seek opportunities to expand our knowledge. The place to build a long-term meaningful career. We have a range of Medical Writing opportunities available across the early and late portfolio including Director, Principal and Senior Medical Writing roles. As a team, we author clinical and regulatory documents that align with project strategies, regulatory requirements and communications best-practices. We support Astra Zeneca's core therapeutic areas in all phases of clinical development, playing a key part in delivering medicines to patients most in need as swiftly as we can. Whichever role you're successful in, you'll be joining an extraordinary team who has an outstanding record of achieving successful submissions and approvals. Each role will afford you flexibility in ways of working. Essential for the role We believe that you hold a Bachelor's degree in life sciences at a minimum, and if you have a MSc or Ph D, this will be an advantage. Your education is further complemented by regulatory writing experience from the pharmaceutical industry. Collaboration is key and you have a track record of running fruitful and effective partnerships, both internally and externally. We also believe that you share our passion for applying Medical Writing expertise to reach our goal to change lives. * Solid understanding of the clinical drug development process with experience in integrating information from all phases of clinical development into clinical and regulatory documents and submissions * Extensive knowledge of current regulatory guidelines relating to regulatory communications * Consistent display of ability in project management, thinking (conceptual, analytical and integrative), influencing and team working * Flexibility in adapting to changing circumstances or new information The recruitment process will follow the below steps: Application and CV review 30 minute screening call with a senior member of the team Completion of a medical writing exercise Informal meeting of various team members Final interview Pioneer a new future to meet global healthcare challenges At Astra Zeneca, we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There's no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development. We strongly believe that everyone contributes with a unique set of competence. Your curiosity and passion for personal development combined with support from colleagues, mentors and leaders, will ensure you maximise your skills, abilities and contribution. So, what's next? Are you already imagining yourself joining our team? Good, because we can't wait to hear from you. This role is open from March 24, 2021 and we welcome your application no later than April 15, 2021. Where can I find out more? Our Gothenburg site: https://www.astrazeneca.com/our-science/gothenburg.html Life in Gothenburg: https://www.movetogothenburg.com/ About Bio Pharmaceuticals R&D: https://www.astrazeneca.com/r-d.html

Astrazeneca AB


  • Antal platser: 1
  • Timmar per vecka: 32 - 40 timmar
Sista ansökningsdag: 2021-04-14
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