Senior Regulatory Affairs Consultant - Clinical Writing

AMAZING OPPORTUNITY TO PARTNER WITH AN INNOVATIVE, LARGE GLOBAL PHARMACEUTICAL COMPANY AND GROW PROFESSIONALLY.

If you love clinical regulatory writing, have past experience with Oncology, Rare Disease, or Infectious Disease products, and are looking for an opportunity that will allow you to continue to have the flexibility of working from home while gaining tremendous professional experience and working with some of the Industry’s BEST, then Parexel's Regulatory Consulting team has an amazing opportunity for you!

As a Regulatory Affairs Senior Consultant, you will:

Be responsible for Regulatory technical writing (clinically focused) to support development of clinical documents in accordance with ICH/E6/GCP guidelines to support US/EMA submissions, clinical trial applications, and clinical consultation responses.

Qualifications:

• RA professional with 7+ yrs experience in clinical development that includes writing of clinical technical documents and a strong understanding of ICH/E6/GCP guidelines.

  • Primarily seeking an experienced Clinical author to support FDA submissions:

    • New INDs

    • Pediatric Plans, Fast Track Applications, Breakthrough Therapy Applications, Orphan Drug Applications, responses to FDA requests, Meeting Request and Packages

    • NDA/BLA submissions

• Ability to interpret data and advice from regulatory authorities objectively, often in the face of strongly held competing views.

• Extensive experience of all phases of the drug development process in regulatory affairs, including projects with little or no precedence.

• Extensive knowledge of being able to develop product/therapeutic knowledge in a new area.

• Previous experience independently authoring clinical modules for FDA submissions is required. EU submissions experience is a plus.

• Bachelor’s, Master’s or PhD in science/biological or healthcare.

This role may require

East coast candidates in the US or Canada are strongly preferred based upon the needs of the Client.

Employment is contingent on disclosure of your COVID-19 vaccination status and, if relevant, proof of vaccination.

EEO Disclaimer

Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the United States includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.