drjobs Director Reg Drug Proj Del العربية

Director Reg Drug Proj Del

Employer Active

The job posting is outdated and position may be filled
drjobs

Job Alert

You will be updated with latest job alerts via email
Valid email field required
Send jobs
Send me jobs like this
drjobs

Job Alert

You will be updated with latest job alerts via email

Valid email field required
Send jobs
Job Location drjobs

Gaithersburg - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Job Description

Job Title: Director Regulatory Affairs

Location: Gaithersburg MD (Hybrid)

Duration: 06 Months

Please Acknowledge.

What Youll do

  • As a Regulatory Affairs professional within AstraZeneca you will play a key role in channeling our scientific capabilities to make a positive impact on changing patients lives. In Regulatory Affairs our teams influence the development of our innovative pipeline define the regulatory strategy for our therapeutic assets and engage with Health Authorities to effectively inform our development programs. In this way our Regulatory
  • Affairs teams are transforming exciting science into valued new medicines for patients around the world.
  • Strategic thinking is key within our function. The more experienced you are the more accountability you will have for strategic leadership including responsibility for development and implementation of the global regulatory strategy for a product/group of products of increasing complexity.
  • Essential for the role
  • In combination with your regulatory expertise successful candidates will demonstrate competencies of strategic thinking strategic influencing innovation initiative leadership and excellent oral and written communication skills. It is important that you embrace the concepts of novel regulatory tools and technology as well as a culture of sharing experiences with others so that the medicines that we develop will benefit from latest approaches in regulatory science. You are comfortable speaking the regulatory voice at all levels of the organization.
  • Academic degree in a science related field or equivalent
  • Extensive knowledge of regulatory affairs within one or more therapeutic areas in early and late development
  • Proven track record of regulatory drug development including product approval/launch.
  • Experience in leading Major Health Authority interactions
  • Ability to think strategically and critically and evaluate risks to regulatory activities.
  • Ability to work strategically within a complex business critical and highprofile development program.

Employment Type

Full Time

Company Industry

About Company

Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.