Regulatory Affairs Manager (EAP/Managed Access) - Global Clinical Trial Services - Hybrid Opportunity
Are you ready to advance your career and join a business who are a leader in Clinical Services? Providing the opportunity to specialise in a niche area of a business who have 3 key divisions, providing exposure to an area of the pharmaceutical industry being directly involved in saving the lives of some of the most vulnerable patients in the world.
As part of our close-knit regulatory team of three, you'll dive into developing intelligence materials, creating regulatory plans, and offering project-based support. You'll need a solid grasp of EU directives, US CFR, and GMP/GDP regulations.
Why this role?
- You can delve into a classic RA position, with a fantastic team of specialists
- Opportunities to progress, learn new things in a fast paced environment!
- This businesses passion trumps any other, truly matching your work ethic and in an extremely patient focussed space
- One of the biggest service provider of this specialist area
- Giving someone the freedom to shape key parts of the reg team and function
Alternate Job Titles:
RA Manager / RA Specialist / Regulatory Affairs Specialist / Reg Affairs Specialist / QA Manager / Quality Assurance
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Regulatory Affairs Manager employer: Verbatim Pharma
Verbatim Pharma is an exceptional employer that prioritises a supportive and collaborative work culture, allowing Senior Recruitment Consultants to thrive in a fully remote environment. With a focus on personal development through tailored training opportunities and an industry-leading commission structure, employees can enjoy a fulfilling career while achieving a healthy work-life balance, including the unique benefit of unlimited holiday. Join a family-oriented team that values relationships and encourages you to excel without the pressure of unrealistic KPIs.
