Regulatory Affairs Coordinator Salary in Maryland

Regulatory Coordinator I Sewickley, PA 15143 6 Months Contract Job Description Candidate will review internal and external products and raw materials to evaluate hazards and assign transportation classifications and maintain regulatory compliance in this entry-level scientific, non-laboratory position. We are looking for a team player who is self-motivated, able to maintain high quality while handling repetitive tasks, and manage multiple projects. RESPONSIBILITIES - Work as part of team that provides support to all SW business units - Apply GHS and Transportation regulations to assess product hazards - Use outside vendor SDS to assess transport hazards - Use in-house computer systems to assign transport classifications - Assist with overflow regulatory compliance projects as requested QUALIFICATIONS - Bachelor’s degree in Chemistry, Biochemistry, Biology, or related science - Familiarity with regulatory programs - DOT/Transport preferred - Working knowledge of Safety Data Sheets (SDS)

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

General Summary: The Regulatory Affairs Coordinator (RAC) will work with investigators, study staff, Institutional Review Boards (IRB), clinical trial sponsors and federal regulatory agencies to ensure that regulatory requirements are met for clinical trials. This role reports to the Regulatory Affairs Project/Program Manager and works closely with research teams across the Cancer Center to ensure regulatory compliance for multiple cancer trials. Detailed Responsibilities include managing the following for multiple studies: * Preparation and submission of clinical trials to the local and central IRB(s). * Creation and extensive revisions of informed consent documents * Tracking and facilitating the progress of new trials through the review process * Correspondence with the IRB of record, investigators, and sponsors throughout the review process * Collection, completion, and submission of regulatory documents to various regulatory entities. This includes collecting signatures and inform

General Summary: The Regulatory Affairs Coordinator (RAC) will work with investigators, study staff, Institutional Review Boards (IRB), clinical trial sponsors and federal regulatory agencies to ensure that regulatory requirements are met for clinical trials. This role reports to the Regulatory Affairs Project/Program Manager and works closely with research teams across the Cancer Center to ensure regulatory compliance for multiple cancer trials. Detailed Responsibilities include managing the following for multiple studies: * Preparation and submission of clinical trials to the local and central IRB(s). * Creation and extensive revisions of informed consent documents * Tracking and facilitating the progress of new trials through the review process * Correspondence with the IRB of record, investigators, and sponsors throughout the review process * Collection, completion, and submission of regulatory documents to various regulatory entities. This includes collecting signatures and inform

Regulatory Coordinator I Sewickley, PA 15143 6 Months Contract Job Description Candidate will review internal and external products and raw materials to evaluate hazards and assign transportation classifications and maintain regulatory compliance in this entry-level scientific, non-laboratory position. We are looking for a team player who is self-motivated, able to maintain high quality while handling repetitive tasks, and manage multiple projects. RESPONSIBILITIES Work as part of team that provides support to all SW business units Apply GHS and Transportation regulations to assess product hazards Use outside vendor SDS to assess transport hazards Use in-house computer systems to assign transport classifications Assist with overflow regulatory compliance projects as requested QUALIFICATIONS Bachelors degree in Chemistry, Biochemistry, Biology, or related science Familiarity with regulatory programs - DOT/Transport preferred Working knowledge of Safety Data Sheets (SDS) preferred Experi