Makro Scientific:

Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations.

Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent.

• This individual will be part of the Global Regulatory Affairs team and assists with planning, writing, compilation, and editing of periodic regulatory reports (i.e. DSURs, orphan annual updates, NDA annual reports, PBRERs). 
• With oversight and guidance, contributes to the generation of product regulatory strategy documents (for products in phase 1-3 clinical development), labeling updates for marketed products, generation of FDA meeting requests and corresponding briefing materials, and other tasks as needed.

• Working knowledge of FDA and ICH requirements for standard regulatory documents and their maintenance.
• Excellent written and verbal communication skills, with ability to organize and manage multiple priorities.
• Proficiency in MS Word, Excel, and PowerPoint.
• Self-starter with the ability to work independently but seeking out guidance as needed.
• Technical aptitude to work across multiple information systems and databases with ability to troubleshoot.
• Sense of urgency and perseverance to achieve results.

• Bachelor's degree and at least 5 years in Regulatory Affairs or relevant industry experience, or
• Master's, PharmD, PhD degree and 3 years in Regulatory Affairs or relevant industry experience.