Regulatory Affairs Associate

Parexel

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profile Job Location:

Bengaluru - India

profile Monthly Salary: Not Disclosed
Posted on: Yesterday
Vacancies: 1 Vacancy

Job Summary

When our values align theres no limit to what we can achieve.

At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us no matter what we do at Parexel contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally we do it with empathy and were committed to making a difference.

Regulatory Affairs Associate

2 to 5 years of experience in Regulatory Affairs-CMC should be willing to work in EU Shifts.

To understand the regulatory framework including regional trends for various types of applications and procedures for small and large molecules across all regions.

To provide regulatory input on procedural and CMC documentation requirements specific to as defined by Health Authorities for assigned deliverable(s) including:

o Submission delivery strategy

o Review of documents

o Analysis of regulatory procedures and special designations used during development authorizations and extension of the product.

Liaise closely with cross-functional members with aligned product responsibilities.

Develop execute and maintain submission delivery plans submission content plans and proactively provide status updates to designated stakeholders.

Authoring the dossier sections based on the changes to approved MAA

Knowledge of change evaluation according to country guidelines

Experience in managing lifecycle activities in the EU markets would be preferrable

Knowledge of CTD guidelines.

Review dossier submit dossier negotiate with HA on approval.

Work with local Regulatory medical marketing and market access to support impact of changes


Required Experience:

IC

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...
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Key Skills

  • Proofreading
  • Adobe Acrobat
  • FDA Regulations
  • Manufacturing & Controls
  • Biotechnology
  • Clinical Trials
  • Research & Development
  • GLP
  • cGMP
  • Product Development
  • Chemistry
  • Writing Skills

About Company

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Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our the ... View more

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