Public affairs • phoenix az
The Regulatory Coordinator is responsible for the coordination, preparation, and maintenance of regulatory documentation and compliance for clinical trials.This role ensures adherence to local, sta... Show more
Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team?.MMS is an award-winning, data-focused clinical research organizat... Show more
Public Area Attendant, Courtyard Happy Valley Phoenix North.Join a 2026 USA Today Top Workplace Winner!.This position comes with a $1,000 SIGN ON BONUS!!****.Must be available to work 5 days a week... Show more
Director, US State Government Affairs.Corning is one of the world's leading innovators in glass, ceramic, and materials science.From the depths of the ocean to the farthest reaches of space, our te... Show more
Tetra Tech is adding experienced Disaster Recovery / Grant Management / Public Assistance Consultants to our Disaster Recovery team to support current and future disaster recovery operations throug... Show more
The Principal Regulatory Affairs Specialist role is responsible for preparing and submitting the appropriate documentation for the submission of pre-market applications, periodic updates and regist... Show more
Disaster Recovery / Grant Management / Public Assistance Consultant.Tetra Tech is adding experienced Disaster Recovery / Grant Management / Public Assistance Consultants to our Disaster Recovery te... Show more
Growing CPA firm in Phoenix, Arizona is looking to add a couple Tax Seniors to their staff.Attains specialized knowledge in at least one area of individual or business taxation.Prepare individual a... Show more
Work on transactional matters in the regulatory space.Draft, review, negotiate complex industry agreements.Support deals involving generators, transmission systems, and large load customers.Handle ... Show more
Our mission's simple: every child deserves a safe, loving home, and we're making that real.The Center for the Rights of Abused Children brings Americans together to do more and change more for abus... Show more
We are seeking a dynamic and experienced Public Relations Specialist to join our team and help shape the public image of our organization.This role is perfect for a creative and detail-oriented pro... Show more
Tax Manager - Public Accounting.Salary: $90,000 - $120,000 per year.Growing CPA firm in North Phoenix is looking to add a Tax Manager to their staff.If you are waiting to become a Partner in a well... Show more
Disaster Recovery / Grant Management / Public Assistance Consultant.Tetra Tech is adding experienced Disaster Recovery / Grant Management / Public Assistance Consultants to our Disaster Recovery te... Show more
Disaster Recovery / Grant Management / Public Assistance Consultant.Tetra Tech is adding experienced Disaster Recovery / Grant Management / Public Assistance Consultants to our Disaster Recovery te... Show more
One Source Housekeeping Solution separates itself from the competition by focusing exclusively on the hospitality sector.Through continual investment in our people, our technology, our processes, a... Show more
Director, Field Medical Affairs Hematologic Malignancies (AML).Join a team advancing innovation in hematologic malignancies.IQVIA is seeking an experienced field medical leader to direct a field-b... Show more
Regulatory Affairs Specialist III.The Regulatory Affairs Specialist III works with a team of regulatory affairs professionals to ensure the establishment of best practices within the assigned area ... Show more
Growing CPA firm with locations in Chandler and Scottsdale, Arizona is looking to add a Senior Auditor to their staff.Build relationships with clients by gathering information, resolving problems, ... Show more
IntroductionWe are seeking a motivated and professional Public Relations Assistant to support outreach, communications, and brand engagement initiatives.This role is ideal for individuals who enjoy... Show more
Sonar Spark is a forward-thinking communications and branding firm dedicated to helping organizations shape meaningful narratives and build lasting connections with their audiences.We combine strat... Show more
The average salary range is between $ 57,843 and $ 123,256 year , with the average salary hovering around $ 72,000 year .
The average salary range is between $ 62,123 and $ 148,063 year , with the average salary hovering around $ 89,089 year .
The Regulatory Coordinator is responsible for the coordination, preparation, and maintenance of regulatory documentation and compliance for clinical trials. This role ensures adherence to local, state, and federal regulations, including but not limited to FDA, ICH, and GCP guidelines, and supports the smooth conduct of clinical research studies at the site. They will support clinical research teams by facilitating the study start-up approval process and maintaining documentation of regulatory compliance throughout the trial's duration for research studies involving human subjects. S/he will be responsible maintaining accurate and up-to-date regulatory files. S/he will serve as a central regulatory resource for staff conducting clinical research. This position reports to the Director of Research Services. Prepare, review, and submit regulatory documents for initial IRB submission, amendments, continuing reviews, and protocol deviations. Reviews informed consents for institutional language and work with legal and sponsors to ensure CTA language is consistent with consent. Maintain accurate and up-to-date regulatory binders, including signed investigator agreements, CVs, and medical licenses. Develop and maintain electronic regulatory files in compliance with institutional and sponsor requirements. Track protocol approvals, renewals, and amendments to ensure study compliance. Monitor study compliance with federal regulations (FDA, OHRP) and guidelines (ICH, GCP). Maintain site readiness for internal and external audits and inspections, including preparing regulatory files and ensuring proper documentation Assist in preparing responses to audit findings and implementing corrective actions. Ensure prompt and accurate reporting of adverse events (AEs), serious adverse events (SAEs), and protocol deviations. Provides study updates, deviations, and SAE reports to Director of Research Services.
Bachelor's degree required Minimum of 2 years of experience in regulatory coordination within clinical research, preferably in oncology. Knowledge of FDA regulations, ICH guidelines, and GCP standards. Experience with IRB submissions, protocol amendments, and regulatory document management. Experience working with multiple central IRBs, understanding their submission process and requirements. Proficiency with electronic systems and Microsoft Office Suite. Strong organizational skills, attention to detail, and ability to manage multiple tasks efficiently.
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