Find & Apply For Regulatory Affairs Manager Jobs In Wake, North Carolina

Regulatory Affairs Manager jobs in Wake, North Carolina involve ensuring compliance with regulations, preparing documentation, and communicating with authorities. Responsibilities may include developing strategies, conducting research, and staying updated on industry standards. Strong communication, analytical, and organizational skills are essential for success in this role. Below you can find different Regulatory Affairs Manager positions in Wake, North Carolina.

Latest Jobs in Wake

Salary Information & Job Trends In this Region

Regulatory Affairs Managers in Wake, North Carolina oversee compliance with regulations in the pharmaceutical and medical device industries. - Entry-level Regulatory Affairs Specialist salaries range from $60,000 to $75,000 per year - Mid-career Regulatory Affairs Manager salaries range from $80,000 to $100,000 per year - Senior Regulatory Affairs Director salaries range from $110,000 to $150,000 per year The role of Regulatory Affairs Manager has a rich history in Wake, North Carolina, dating back to the establishment of the Research Triangle Park in the 1950s. This area has become a hub for pharmaceutical and biotechnology companies, driving the need for professionals to navigate regulatory requirements. Over the years, the position of Regulatory Affairs Manager has evolved to encompass not only ensuring compliance with FDA regulations but also global regulatory standards. With advancements in technology and changes in the regulatory landscape, Regulatory Affairs Managers play a crucial role in bringing new products to market while ensuring patient safety. Current trends in the field of Regulatory Affairs in Wake, North Carolina include a focus on digital submissions for regulatory approvals, increased collaboration with international regulatory agencies, and the adoption of risk-based approaches to compliance. Regulatory Affairs Managers are also at the forefront of incorporating real-world evidence into regulatory submissions to demonstrate product effectiveness in diverse patient populations.

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