Senior Manager, Regulatory Affairs
- Raleigh, Blue Bell
- ICON Full Service & Corporate Support
- Drug / Device Regulatory Affairs
- 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.
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Learn more about Our Culture at ICON
Day in the life
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Location
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Remote Working
Hybrid: Office/Remote
Business Area
ICON Full Service & Corporate Support
Job Categories
Drug / Device Regulatory Affairs
Job Type
Permanent
Description
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Reference
JR129102
Expiry date
01/01/0001
Author
Caroline LockAuthor
Caroline Lock