Modis / Astra Zeneca

Regulatory Project Manager

About Modis We are constantly striving to support our customers and consultants to become successful. As a consultant, you are our top priority and when you need us, we will be there for you. We will include you in our business and to our customers. You are our most important asset and for us to stay ahead you will take an active part in our business development and our offers to the market. By becoming our colleague, your daily life as a consultant will be shifting with different assignments and projects in a variety of industries, systems and environments. Your experience will increase as well as your social and professional network. As a consultant, you are covered by collective agreements, insurance, occupational healthcare, healthcare and discounts on training cards. We believe in connecting people so having regularly social activities is key for us. Modis delivers a wide range of services and competencies within IT, Engineering and Life Science. Our services are characterized by speed, simplicity and quality. Modis is represented in the United States, Canada, Europe with over 100 offices and with more than 35,000 colleagues on assignments each day.
den 29 juli 2018
Förväntad start.
den 1 september 2018
Antal timmar
Sverige > Göteborgs stad > Västra Götalands län

Modis Life Science is looking for a regulatory Project Manager to AstraZeneca, Gothenburg!
The consultant assignment will start 2018-09-18 and proceed for one year.

Welcome with your application no later than August 14th.

AstraZeneca is a science-led, global biopharmaceutical company, with a focused portfolio in core therapies. We are committed to improving the health and lives of people across the globe, through our broad research and development platform, and a growing late-stage pipeline. Working in over 100 countries, we have strength in most global markets. Our medicines are used by millions of patients and clinicians worldwide.

The arena

The Regulatory Project Management (RPM) is a group within the AZ Global Regulatory Affairs, Patient Safety and QA (GRAPSQA) organization. RPM is accountable for end to end regulatory submission delivery, providing regulatory expertise, efficient project management and strong leadership in line with business priorities. The RPM is allocated to project teams with the responsibility to plan, prepare and deliver various types of regulatory submissions.

We now have a temporary position in our team for one year.


  • Project manage (plan, prepare, coordinate and deliver) submission in accordance with agreed plans.
  • Develop, execute and maintain submission plans and proactively provide status updates to designated stakeholders. 
  • Identify potential regulatory risks to the operational plans and propose options to mitigate these. If required, lead sub-teams to deliver regulatory submissions.
  • Provide operational regulatory input and guidance with respect to regulatory submissions.
  • Ensure that appropriate, up-to-date records are maintained for compliance.
  • Use and share best practices, when handling various applications and procedures.

Preferred skill/experience:

  • University Degree in Science or related discipline
  • Project Management experience
  • Relevant regulatory experience or experience elsewhere in Pharmaceutical Industry
  • Knowledge of the drug development process
  • Excellent written and verbal communication skills
  • Global team experience

Arbetstid / Varaktighet

The consultant assignment will start 2018-09-18 and proceed for one year.

Skicka din ansökan

If you have questions regarding the position, please contact:

Nalin Yilmaz

Anneli Bermbeck

Anders Olsson

Welcome with your application no later than August 14th.

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Modis / Astra Zeneca

Modis / Astra Zeneca

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