Regulatory Affairs Coordinator Salary in Alabama

Regulatory Affairs Expert-Medical Devices 1 Year (Temp to perm) St Louis, MO (Hybrid 2-3 days onsite) Pay: $33.00/hr Your Role: With minimal supervision, the Regulatory Affairs Expert-Medical Devices manages assigned regulatory tasks related to health authority notifications, submissions, and registrations regarding renewals and new products, and changes to products or sale of products ensuring continual compliance to all applicable regulations and ensuring that site regulatory strategy aligns with overall corporate regulatory strategy, goals, and objectives. Responsibilities Independently assemble and maintain technical files and other regulatory documentation to ensure timely registrations and renewals Maintain library/database of technical documentation Monitor the status of standards and regulations. Conduct a review and analysis in case if requested. Assist and advise in activities related to regulatory registrations, listing, and regulatory compliance, with particular focus on In

Overview Join the HJF Team! HJF is seeking a Regulatory Affairs Coordinator to be responsible for assisting in the compliance of HJF research programs with applicable local, state and federal regulations for human subjects research, animal use research, recombinant DNA, and Health Insurance Portability and Accountability Act (HIPAA). This is the first level in the Regulatory Affairs series. This position will be in support of the Office of Regulatory Affairs & Research Compliance at the Home Office in Bethesda, MD. The Henry M. Jackson Foundation for the Advancement of Military Medicine (HJF) is a nonprofit organization dedicated to advancing military medicine. We serve military, medical, academic and government clients by administering, managing, and supporting preeminent scientific programs that benefit members of the armed forces and civilians alike. Since its founding in 1983, HJF has served as a vital link between the military medical community and its federal and private partners

Recent Pharma/ CRO experience required Regulatory Operations Contractor Regulatory Affairs Location(Boston) Contract Term: Contract through EOY with possible extension Should have strong Word, PDF, Adobe skills – going through documentation, cleaning it up, getting approvals, submissions, sending out to Reg Document publishing is key, submission publishing with document publishing is even better Supported preparation of NDA and created project plans for NDA modules Extensive bookmarking and hyperlinking, taking all the submission documents and hyperlinking all the supporting study data and reports. Position Summary: Reporting to the Senior Director, Regulatory Operations, the Regulatory Operations Contractor will assist with the development and implementation of systems and procedures used to support regulatory submission activities including eCTD production, document publishing, and document management. This position will also be responsible for participating in day-to-day Regulatory

Company Description At BilliMD, we specialize in simplifying medical billing and revenue cycle management. Our end-to-end solutions integrate seamlessly with EHR/EMR systems, freeing your staff from manual tasks and allowing them to focus on patient care. We have a team of certified coders, seasoned professionals, and healthcare experts who are dedicated to ensuring efficiency and precision in revenue cycle management, medical coding, and credentialing. Our commitment to operational excellence includes diligent claim monitoring, error minimization, and transparent financial performance analysis to help maximize your revenue. Role Description This is a full-time on-site role as a Credentialing Specialist located in Miami, FL. As a Credentialing Specialist at BilliMD, you will be responsible for managing credentials, renewals, and providing maintenance and support. The Credentialing Specialist is responsible for coordinating, monitoring, and maintaining the credentialing and re-credentia

Massey Comprehensive Cancer Center The Massey Comprehensive Cancer Center has an exciting opportunity for an Regulatory Affairs Coordinator to join our team! Our employees and applicants come from diverse backgrounds. We hire great people from a wide variety of backgrounds, not just because it's the right thing to do, but because it makes VCU stronger. "To improve the lives of all Virginians by delivering cutting-edge cancer care through patient-centered prevention and treatment; high-impact, innovative research; community input and engagement; and education and training of the next generation of researchers and healthcare professionals." Virginia Commonwealth University (VCU) Massey Comprehensive Cancer Center is a nationally ranked cancer center located in the heart of Downtown Richmond. All full-time staff is eligible for our generous benefits package that includes choices for health, vision, and dental coverage, life insurance, short and long-term disability coverage, retirement pl

JOSIE MARAN REGULATORY AFFAIRS COORDINATOR WHO WE ARE Josie Maran is the pioneer of clean, Argan oil-powered beauty. The first to champion the natural potency of pure oils, we are now the leading innovator in clean beauty. Sourced from a UNESCO-protected region in Morocco, 100% Pure Argan Oil is the center of everything we do—from our skin-transforming products to our collaboration with women’s co-ops and Earth-first sustainability platform. Our cruelty-free formulations honor inclusivity from soil to seed to bottle and are safe and effective for every skin type and lifestyle. We believe in the vibrational energy of conscious skincare. It is a community-centered effort, with a responsibility to support the environment, nurture the self, and cultivate joyful human connection. We celebrate the radical courage behind bare skin, and the reverberating effects of nourishing yourself from the inside out. We are an equal opportunity employer. We value diversity and prohibit discrimination and