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Regulatory Affairs Associate

Bengaluru, Karnataka, India Date posted 05/22/2021 Job ID 69865BR

As part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter – and keeping them there –your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical device companies large and small.

In return, you will be provided with interesting opportunities for growth and development and exposed to a variety of challenging assignments, product types, geographic regions, and therapeutic areas. Plus, as member of Parexel Consulting, you will enjoy all the advantages of working remotely, combined with access to the mentorship from a team of highly experienced regulatory professionals at the height of their careers. Join our team, and you will design solutions for the complexities of an ever-changing global marketplace.

Success Profile

Check out the top traits we're looking for and see if you have the right mix.

  • Detail-Oriented
  • Proactive
  • Problem-Solver
  • Results-Driven
  • Organized
  • Multi-Tasker
  • "When submitting major market applications, it’s key to ensure that the technical integrity of all data meets regulated requirement standards. Parexel makes this possible with a diverse team of seasoned professionals who care about getting important medicines to patients. This is Regulatory Operations at its best."

    Chris – Associate Director, Regulatory & Access
  • "In this role, I have had the unique opportunity to work with regulatory experts who are not only some of the most distinguished in their field, but are also some of the most compassionate people I know. I’ve been able to grow so much professionally by standing on the shoulders of giants!"

    Riley – Regulatory Affairs Consultant


  • Global Impact

    We are one truly global team working together to propel each client´s journey ahead faster.

  • Balance

    We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.

  • Collaboration

    Work with industry leaders and subject matter experts.

  • Freedom

    The ability to innovate, ask “what if” and try new solutions without fear of failure.

  • Variety

    Opportunities to work on multiple accounts – never boring!

  • Management

    Strong management with depth of experience working for global health authorities.


Supports SME team or acts as the SME to provide content to client proposals and scoping. • Mentors and trains junior team members/new joiners.• Assures proactive collaboration with internal team; elevates agenda items for meetings, or emails, or conversation; and works with cross SBU counterparts or line manager to solve issues and eliminate barriers for project deliverables.• Prepares and/or delivers a presentation internally with Project Team and externally with client (e.g., Kick off Meetings with client, or Bid Defense Meeting).• Provides technical consulting services or expertise within specialist area (e.g., CMC, Nonclinical, Clinical, Labeling). Works with the sponsor/client to draft master label of IMP and provides instruction to each country label reviewer for completing IMP label review. • Proactively assesses and discusses with his/her PL and/or client concerns associated with regulatory compliance, and provides associated guidance, that results in clients expressing satisfaction with service provided.• Independently prioritizes work load to effectively deliver all assigned work on time.• Reaches out to the appropriate team member to discuss and address issues associated with deliverables, and shares perspective and seeks the perspective of others to come up with the best solution.• Serves as a Project Lead for small-scale projects, as a Regulatory Lead or a Subject Matter Expert on larger projects, or as a Portfolio/Workstream Lead on larger projects.


Masters in Pharmacy or Life sciences

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