Quality and Regulatory Specialist - Irving, TX

This role is unique as it serves as the primary onsite expert for all US-based quality and regulatory activities. · We are looking for a seasoned quality professional with a background in science or engineering to become the high-visibility subject matter expert for an entire reg ...

· Regulatory Operations Specialist (PECOS, Vendors & Credentialing) · Position Summary · The Regulatory Operations Specialist supports day-to-day PECOS filings, vendor regulatory documentation, and provider credentialing activities. This role is execution-focused and detail-driv ...

· Description · Regulatory Operations Specialist (PECOS, Vendors & Credentialing) · Position Summary · The Regulatory Operations Specialist supports day-to-day PECOS filings, vendor regulatory documentation, and provider credentialing activities. This role is execution-focused a ...

· Join Life Care Home Health Family  · Serving Texas, Florida, Nevada, and Georgia, we provide skilled nursing, therapy, homecare, hospice, palliative care, and private duty services. · Why Work With Us? · Nestmed AI Scribe: Less charting, more caring · Competitive pay, 401k, he ...

+iRely is seeking an experienced and detail-oriented Regulatory Contract Specialist to support our growing US and International operations. · +Review and monitor regulatory requirements in countries where the company operates (U.S., India, Philippines, and others as applicable). ...

The Regulatory Maintenance Specialist ensures research compliance protocols, · federal regulations, industry guidelines and company Standard Operating Procedures. · ...

+Job summary · iRely is seeking an experienced Regulatory Contract Specialist to support its growing US and International operations.++Bachelor's degree in business, Finance, Legal Studies, or related field (J.D. preferred but not required). · 5+ years of experience in contract r ...

+The Regulatory Maintenance Specialist ensures research compliance protocols, federal regulations, industry guidelines, and company Standard Operating Procedures. · ...

The Regulatory Operations Specialist supports day-to-day PECOS filings, vendor regulatory documentation, · and provider credentialing activities. · Maintain regulatory trackers, calendars, · and filing logs. · ...

Regulatory Operations Specialist (PECOS, Vendors & Credentialing) · Position Summary · The Regulatory Operations Specialist supports day-to-day PECOS filings, vendor regulatory documentation, and provider credentialing activities. This role is execution-focused and detail-driven, ...

+The Regulatory Operations Specialist supports day-to-day PECOS filings, vendor regulatory documentation, and provider credentialing activities. · +Prepare and submit PECOS enrollments, revalidations, and updates under supervision. · Collect, organize, and maintain required owner ...

This position will provide full regulatory support to the Department of Urology which has approximately 36 faculty. · Prepares, submits, and revises all IRB or IACUC applications. · Responsible for the review and initial start-up of budgets · ...

We are seeking a Regulatory Affairs Associate Specialist to support McKesson's Controlled Substances Monitoring Program (CSMP). The role will provide administrative support to the Regulatory Affairs Department, conduct initial customer due diligence, and use tools, reports, and d ...

We are seeking a Regulatory Affairs Associate Specialist. This role is a work-from-home position in the Dallas-Fort Worth Metropolitan area. If the applicant is located outside of the area, they must be willing to relocate. · Responsibilities:Organize and coordinate incoming regu ...

This position will provide full regulatory support to the Department of Urology which has approximately 36 faculty.This position will work closely with investigators and research personnel on the development and refinement of proposals for the performance of human clinical trials ...

The Sr.Regulatory Affairs Specialist plays a critical role in ensuring McKesson's compliance with Controlled Substances Monitoring Program (CSMP) policies and procedures... · Design and support processes to monitor ongoing compliance with CSMP policies and procedures. · ...

Position Purpose: · The position of Regulatory Compliance Specialist is centered on ensuring adherence to pertinent local, state, and federal regulations by collaborating closely with the Regulatory Compliance Managers. This role demands a proactive approach in submitting and pro ...

We are seeking a Regulatory Affairs Specialist II to support the European Union In Vitro Diagnostic Regulation (IVDR) transition efforts impacting Bio-Rad products currently CE-marked under the IVD Directive.This role will focus on technical file remediation labeling conversions ...

Join our client's Regulatory Affairs team to support the transition to the EU's In Vitro Diagnostic Regulation (IVDR). This role plays a critical part in ensuring regulatory compliance by revising technical documentation, updating labeling, and coordinating regional notifications ...

+The Clinical Regulatory Specialist provides documentation coordination for Medicare and Non-Medicare Payors, as well as medical records requests from outside entities. · ++Demonstrate in-depth knowledge of EMR privacy and confidentiality rules and regulations and adheres to HIPP ...