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Senior Manager, Regulatory Affairs

  1. Raleigh, Blue Bell
JR101356
  1. ICON Full Service & Corporate Support
  2. Drug / Device Regulatory Affairs
  3. Remote

About the role

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Raleigh/Durham or Remote role

At ICON, it’s our people that set us apart.

As a global provider of drug development solutions, our work is serious business. But that doesn’t mean you can’t have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. Are you one of them?

We are looking for passionate, resilient, and inspiring individuals to join our team. As the Sr Regulatory Affairs Manager, you will represent the Regulatory Affairs function on project teams and client meetings to provide regulatory guidance and strategy.

The role


Job Description Summary

  • Participate in provision of Regulatory expertise in strategic drug development across multiple areas.
  • Take part in preparation of strategic development and submission plans.
  • Be involved in the regulatory affairs activities across the ICON portfolio and be an expert and advisor to ICON clients (externally and Internally)
  • Be a trusted partner - represent the Regulatory Affairs Department in business development activities and generate new business opportunities
  • Contribute to at least two of the following areas: Interactions with Regulatory agencies, early phase consulting, Development Planning (PDP/RDP/CDP), Scientific/Agency advise, orphan drugs/pediatric development, medical devices, Reg Intelligence, due diligence, strategic CT support/GCP compliance, biologlcal/blotech/biosimilars, small company support (incl. SOPs development etc.)
  • As Regulatory Expert, build effective teams and Involve junior members of the team into more complex regulatory issues. Mentor and train across function to support the wider Regulatory Department.

What you need

  • Minimum of a Bachelor’s degree in Regulatory/Life Sciences
  • Minimum of 8-10 years of Regulatory experience in Pharma, Biotech, or related industry
  • Knowledge of IND/NDA/BLA requirements
  • Sound knowledge of the life cycle of a drug development program

Why join us?

Ongoing development is vital to us, and as the Sr Regulatory Affairs Manager, you will have the opportunity to progress your career, with the potential to move into other related areas to enhance your skill set. Our benefits package is competitive, our scope is international and we genuinely care about our people and their success.

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Day in the life

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Reference

JR129102

Expiry date

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Caroline Lock

Author

Caroline Lock
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