Regulatory Affairs Associate

Posted:
4/28/2026, 4:42:31 PM

Location(s):
Karnataka, India ⋅ Bengaluru, Karnataka, India

Experience Level(s):
Junior ⋅ Mid Level

Field(s):
Legal & Compliance

Workplace Type:
Remote

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's 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 we're committed to making a difference.

  • 2-4 yrs yrs in-depth knowledge of Indian regulatory guidelines for clinical trials, including NDCT Rules.
  • Hands-on experience with SUGAM portal for Initial Clinical Trial Application (CTA/iCTA) submissions and amendments.
  • Ability to liaise effectively with global sponsors and cross-functional teams.
  • Prepare necessary documentation, presentations, and briefing materials for SEC meetings
  • Strong understanding of global regulatory expectations and harmonization with Indian requirements.
  • Acquired hands-on expertise in managing and completing clinical trial registrations on the Clinical Trials Registry-India (CTRI) portal.
  • Updated with current Guidelines and Gazette Notifications to give suggestions/comments to respective Regulatory authorities and Govt. regulatory bodies.
  • Working knowledge of India regulatory procedures including adaptability to strict Health Authority and Sponsor timelines for completing submissions
  • Manage timelines for query responses and ensure on-time submission through SUGAM portal or other regulatory platforms.
  • Clear oral and written communication skills
  • Acceptability towards varied cultural mindsets to collaborate efficiently with client counterparts and other internal stakeholders as well
  • Execute and maintain submission delivery plans, submission content plans, and proactively provide status updates to designated stakeholders.
  • Strong communications skills and ability to guide and mentor team members.
  • Ability to work in different time zones
  • Ability to work independently

Parexel

Website: https://www.parexel.com/

Headquarter Location: Waltham, Massachusetts, United States

Employee Count: 10001+

Year Founded: 1982

IPO Status: Delisted

Last Funding Type: Venture - Series Unknown

Industries: Biopharma ⋅ Biotechnology ⋅ Consulting ⋅ Industrial ⋅ Medical Device ⋅ Web Development