Associate Principal Medical Communications Scientist

AstraZeneca / Apotekarjobb / Göteborg
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At AstraZeneca we work together across global boundaries to make an impact and find answers to challenges. We do this with the upmost integrity even in the most difficult situations because we are committed to doing the right thing. We continuously forge partnerships that help pursue world-class medicines in new ways, combining our people's exceptional skills with those of people from all over the globe.

As an Associate Principal Medical Communications Scientist (Strategic Regulatory Writer) in Gothenburg you'll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients' lives. GMD (Global Medicines Development) drives late-stage development of our innovative pipeline, transforming exciting science into valued new medicines and ensuring patients around the world can access them.



Main Duties and Responsibilities

As an Associate Principal Medical Communications Scientist (Strategic Regulatory Writer), you will provide expert communications leadership to late stage drug projects and drive strategic medical writing, advocating communications excellence in your team. He/She ensures that NDA/BLA/MAA/JNDA/CN/ROW clinical documents align with project strategies, meet regulatory requirements and adopt best communications practices.

To be a Strategic Regulatory Writer, you should want to move on from writing study-level documents to authoring more complex documents and submissions, taking on more strategic responsibilities and leading global authoring teams.

• Lead development of the clinical submission communication strategy for a new product, liaising with senior project staff

• Prospectively develop a storyboard for the submission and identify how the proposed prescribing information will be supported

• Lead the authoring of clinical documents for the NDA and MAA

• Author the most complex and important documents (eg, Clinical Overviews, Briefing documents for regulatory authorities and Advisory Committees)

• Lead a team of medical writers (internal and external) to deliver

• Ensure alignment of clinical submission documents with the proposed prescribing information

• Represent medical writing on the high-level, cross-functional submission team



Minimum Requirements

• Bachelor's degree in the life sciences preferably with an MS or PhD.

• Willingness to undertake domestic and international travel as required by the project.



Two years' experience within the pharmaceutical/medical industry/CRO is desirable.



Next Steps - Apply today!



We encourage you to send your application as soon as possible, since interviews will be held continuously.

Welcome with your application no later than October 28th, 2018.

To be considered for this exciting opportunity, please complete the full application on our website at your earliest convenience - it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity. If you know someone who would be a great fit, please share this posting with them.



AstraZeneca is a global, science-driven biopharmaceutical company. We turn ideas into life changing medicines. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. Here, we see the impact of our collective ideas and expertise, and the power of science to deliver them. AstraZeneca is proud to provide a unique workplace culture that inspires innovation and cross-boundary collaboration. Within this environment employees are empowered to express diverse perspectives, and are made to feel valued, energized and rewarded for their ideas and creativity.

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, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law.

Varaktighet, arbetstid
Heltid Permanent

Publiceringsdatum
2018-09-14

Ersättning
Not Specified

Så ansöker du
Sista dag att ansöka är 2018-10-03
Ange följande referens när du ansöker: R-035808
Klicka på denna länk för att göra din ansökan

Kontakt
AstraZeneca jessica.tangefjord@astrazeneca.com

Företag
AstraZeneca

Adress
AstraZeneca
43183
43183 1480

Kontorsadress
Pepparredsleden 1

Jobbnummer
4348950

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