Medical Scientist, Late Oncology
AstraZeneca

Gaithersburg, Maryland

Posted in Pharmaceuticals
about 1 month ago



This job has expired.

Job Description

At AstraZeneca when we see an opportunity for change, we seize it and commit real resources to make it happen, because an opportunity no matter how small can be the start of something big. Delivering life-changing medicine is about being entrepreneurial - finding those moments and recognizing their potential. Big success can come from seeing potential in something small. We empower our people to seek these out, and we support them to pursue the opportunities they find.

Late Stage Oncology is the science engine room for our late stage development. Our strategy and ability to transform our portfolio means we have a late stage pipeline that presents incredible opportunities to push the boundaries of science to deliver life-changing medicines. We transform clinical concepts into medicines that deliver patient health benefits.

In Late Stage Oncology development, we have a crucial role to play. Faced with complex disease challenges, we're focused on exceptional performance to transform innovative molecules into medicines that change lives. We are responsible for enabling the business to make critical pipeline and investment decisions, to ensure they select the right molecules to progress and to seize the right lifecycle management opportunities - generating the data required to drive regulatory submissions for new medicines and expanded indications and generating the evidence that shows their true value.

This is an exciting period for us, as well as for those poised to join us. We are looking for established scientists who wish to broaden their roles. As a Medical Scientist you will have a role in developing new registration-focused trials. You will be working independently with guidance in only the most complex situations and be a close partner to the physician on the team.

Main Duties and Responsibilities

  • You will have key relationships internally with clinical project teams, and externally with regulatory bodies and external service providers.
  • You will ensure there is adequate input into the drug development process from experts in each of the various areas of drug development, or provide input into one or more of these areas as a technical expert.
  • You will develop and design studies to determine the scientific and clinical viability of a particular drug or portfolio of drugs and interpret the results of these studies, either as the head of a team, or by providing expert input.
  • You will participate in protocol design, writing and Implementation to meet GCP, ICH and all AZ quality standards.
  • You will manage cross functional projects to ensure the successful passage of drugs through all phases of the drug development process, or contribute to one or more elements of such a project as a technical expert.
  • You will review and interpret medical data and clinical trial data and come up with conclusions
  • You will also have responsibility for delivery of pieces of the trials and may lead submissions from a process standpoint.


Essential Requirements
  • PhD in a scientific field, PharmD or MD is strongly preferred, candidates with significant relevant drug development experience will be considered
  • Oncology clinical trials experience
  • Experience managing and interpreting the results of clinical trials as well as exposure to writing protocols
  • Strong analytical skills
  • Experience of authoring scientific documents
  • Well-developed communication skills
  • Sufficient technical and disease area knowledge to be able to interact with confidence with internal and external partners


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