Clinical Regulatory Specialist (Bilingual) - 250726 - Doral

The Regulatory Specialist will work as an integral member of the research staff by maintaining day-to-day regulatory tasks within the site network, assisting with the execution of clinical studies in accordance with the protocol, contract scope of work, ICH/GCP, sponsor, CRO, Rov ...

The Regulatory Affairs Specialist is responsible for routine clinical research operations duties in support of clinical trials. · ...

A Tech-savvy Regulatory Specialist with hands-on experience supporting clinical research operations through comprehensive regulatory compliance and document management. · ...

Position Summary: · The Regulatory Specialist will work as an integral member of the research staff by maintaining day-to-day regulatory tasks within the site network, assisting with the execution of clinical studies in accordance with the protocol, contract scope of work, ICH/GC ...

Position Summary: · The Regulatory Specialist will work as an integral member of the research staff by maintaining day-to-day regulatory tasks within the site network, assisting with the execution of clinical studies in accordance with the protocol, contract scope of work, ICH/GC ...

Requisition No: · Agency: Business and Professional Regulations · Working Title: REGULATORY SPECIALIST III · Pay Plan: Career Service · Position Number: · Salary:  Hiring Salary: $1,396.82 to $1,531.54 Biweekly  · Posting Closing Date: 03/08/2026  · Total Compensation Estimato ...

The Regulatory Specialist will work as an integral member of the research staff by maintaining day-to-day regulatory tasks within the site network... · ...

Requisition No: · Agency: Business and Professional Regulations · Working Title: OPS REGULATORY SPECIALIST III · Pay Plan: Temp · Position Number: · Salary:  $21.00 per hour  · Posting Closing Date: 03/17/2026  · Total Compensation Estimator Tool · DIVISION OF ALCOHOLIC BEVERA ...

We are seeking a detail-oriented ,knowledgeable and experience Regulatory Specialist to join our team. · ...

The Regulatory Affairs Specialist is responsible for clinical research operations duties of a routine and technical nature in support of clinical trials.This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG's objectives. ...

This is a contract to hire position for a Regulatory Affairs Specialist responsible for maintaining regulatory compliance. · Maintain regulatory policies and procedures to meet country requirements. · Develop collaborative relationships with functional partners. · ...

We are seeking an enthusiastic hard-working and detail-oriented Regulatory Affairs Specialist responsible for maintaining regulatory compliance. · Direct and coordinate preparation of document packages for regulatory submissions from all areas of the company including internal au ...

· About Company: · Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I–IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience c ...

Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. · The State Personnel System is an E-Verify employer. · This role requires coordinating administrative tasks and/or assignments which are complex in nature. Work involve ...

This is a REGULATORY SPECIALIST II position that assists in coordinating administrative tasks and assignments. · ...

Overview · To maintain control to monitor bureau of customs and border protection (customs), customer and company regulatory activity. Minimize potential liabilities to our customers and FedEx Trade Networks by ensuring that all regulatory activities are performed within time con ...

This position requires experience with technical documentation creation, formatting and coordination. The role involves creating labeling documents and reagent instructions for use documents. · ...

Create labeling documents and reagent instructions for use documents ensure compliance with company standards ISO and GMP. · ...

The Regulatory Specialist will maintain day-to-day regulatory tasks within the site network and assist with clinical studies in accordance with protocol. · ResponsibilitiesPerforms startup activities including IRB submissions. · Assists with management of eRegulatory platform Com ...

This is an Open Competitive Opportunity REGULATORY SPECIALIST II position at the Department of Health in Florida. The incumbent will assist in coordinating administrative tasks, perform indexing, scanning and quality control of investigative documents and case files. · The respon ...