Entry-level Regulatory Affairs professionals that have deep industry knowledge and soft skills that complement your team can be difficult to find. As longtime pharmaceutical industry professionals, we’ve seen this issue time after time.

Through the recent acquisition by Network Partners, FlexPro has launched the Regulatory Affairs Apprentice Leadership Program for pharmaceuticals, providing RA associates who are mentored by colleagues with the level of talent it takes to support pharmaceutical companies. The Apprentice Leadership Program involves rigorous training in unique disciplines by some of life sciences top Subject Matter Experts.

The Importance of Compliance In Regulatory Affairs

Regulatory Affairs Associates help pharmaceutical companies support and address the challenges of meeting strict manufacturing regulations. The Food and Drug Administration (FDA) carefully monitors regulatory submissions to ensure they meet challenging cGxP regulations and guidance.

Regulatory Affairs teams, regardless of size, may struggle with compliance – which is why the Apprentice Leadership Program was created, to provide entry-level talent that is trained within the chosen discipline to help support life sciences projects. Our Regulatory Affairs Associates within the program gain industry knowledge needed to support these projects. On top of our decades of project management expertise, we now offer top-notch Regulatory Affairs Associates to support your team.

How Regulatory Affairs Associates Can Help

Not every entry-level professional in the talent pool is ready on day one, but our Regulatory Affairs Associates are. Their extensive training includes:

• 350+ hours of hands-on classroom training
• Up to 2 years of functional real-world experience gained through the Apprentice Leadership Program
• A focus on leadership and communication skills
• Cross-functional training that deepens their understanding of the profession including working knowledge of the following: project management, packaging and labeling, clinical evaluations, pharmacovigilance, compliance, and medical writing

Projects come up all the time and can cause your team unnecessary stress. Our Associates can support your projects at any level. We’ve found that our clients often ask for Regulatory Affairs Associate’s help with CMC modules and technical writing, which are time-intensive tasks that must be handled with absolute professionalism and attention to detail.

Could your Regulatory Affairs team benefit from some extra help in areas like these? Contact a FlexPro Partner today.

Schedule a 15-minute call with Raquel today to discuss your needs and let’s move those time-consuming Regulatory Affairs projects off your plate and into the finished pile.