| Distance: | Resume alert | Resumes 111 - 120 of 25498 |
Healthcare Outreach & Support Specialist
Phoenix, AZ
... ●Ensured compliance with FDA and ICH guidelines through meticulous administrative support. Enrichment Assistant The Ridges at Peoria — Jun 2021 – Jan 2022 ●Led community-based enrichment programs for residents, focusing on meaningful engagement. ... - Mar 31
... ●Ensured compliance with FDA and ICH guidelines through meticulous administrative support. Enrichment Assistant The Ridges at Peoria — Jun 2021 – Jan 2022 ●Led community-based enrichment programs for residents, focusing on meaningful engagement. ... - Mar 31
Seasoned Technical Writer, Project Coordinator & Business Analyst
Skokie, IL
... This included CER documentation structure for EPA disposal regulations, a scientific term glossary, and FDA / EU MDR regulated procedural manuals. June 2017 - December 2018 Technical Writer/Business Analyst Solution Partners - Pfizer, Lake Forest, ... - Mar 31
... This included CER documentation structure for EPA disposal regulations, a scientific term glossary, and FDA / EU MDR regulated procedural manuals. June 2017 - December 2018 Technical Writer/Business Analyst Solution Partners - Pfizer, Lake Forest, ... - Mar 31
Regulatory & Clinical Trial Startup Expert
Elgin, SC, 29045
... Expertise in IRB submissions, regulatory documentation, and safety reporting ensures adherence to FDA and ICH-GCP standards. Proven track record in managing trial startup activities and maintaining audit-ready files, enhancing operational efficiency ... - Mar 31
... Expertise in IRB submissions, regulatory documentation, and safety reporting ensures adherence to FDA and ICH-GCP standards. Proven track record in managing trial startup activities and maintaining audit-ready files, enhancing operational efficiency ... - Mar 31
Enterprise Architect - Digital Transformation & Cloud Strategy
Morris Plains, NJ
... Instrumented BI systems clinical trial apps with FDA 1572 compliance rules at Organon/Schering-Plough. Re-architected one of most complex solutions, TechAccess at ITS, that reduced OpEx and demonstrated the true value of SOA when done right. ... - Mar 31
... Instrumented BI systems clinical trial apps with FDA 1572 compliance rules at Organon/Schering-Plough. Re-architected one of most complex solutions, TechAccess at ITS, that reduced OpEx and demonstrated the true value of SOA when done right. ... - Mar 31
Strategic Panning, Supply Chain & Materials Leader
Tucson, AZ
... Implemented, changed, and documented procedures in line with all FDA and GMP requirements for a medical device manufacturing site. Reorganized the warehouse to improve material flow and maximize space utilization. Held head count with minimum ... - Mar 31
... Implemented, changed, and documented procedures in line with all FDA and GMP requirements for a medical device manufacturing site. Reorganized the warehouse to improve material flow and maximize space utilization. Held head count with minimum ... - Mar 31
Confidential Background Screening Analyst
Wilmington, NC
... L3 (4745) FACISL-L3 : The FACIS Level 3 sanctions and exclusions search typically includes OIG LEIE, GSA/SAM EPLS, DEA, FDA, TRICARE, OFAC SDN, Medicare Opt-Out, state board and state agency issued sanctions and disciplinary actions from all 56 U.S. ... - Mar 31
... L3 (4745) FACISL-L3 : The FACIS Level 3 sanctions and exclusions search typically includes OIG LEIE, GSA/SAM EPLS, DEA, FDA, TRICARE, OFAC SDN, Medicare Opt-Out, state board and state agency issued sanctions and disciplinary actions from all 56 U.S. ... - Mar 31
Seasoned Administrative Assistant with 40 Years' Experience
Springfield, PA
... Compiled presentations for executive meetings, including updates related to Consent Decree and FDA inspections. Managed spreadsheets, prepared and submitted expense reports, and organized appointments and travel for Worldwide Regulatory Affairs. ... - Mar 30
... Compiled presentations for executive meetings, including updates related to Consent Decree and FDA inspections. Managed spreadsheets, prepared and submitted expense reports, and organized appointments and travel for Worldwide Regulatory Affairs. ... - Mar 30
Clinical Research Coordinator - 20+ Years in Pharma/CRO
Detroit, MI
... Proven expertise in coordinating studies from site initiation through close-out, ensuring full compliance with ICH-GCP, FDA, and IRB guidelines. Skilled in maintaining regulatory documentation, monitoring visit preparation, and managing electronic ... - Mar 30
... Proven expertise in coordinating studies from site initiation through close-out, ensuring full compliance with ICH-GCP, FDA, and IRB guidelines. Skilled in maintaining regulatory documentation, monitoring visit preparation, and managing electronic ... - Mar 30
Strategic Plant Leader in Global Supply Chain
Elkhorn, NE
... Developed compliance quality systems and operations systems remediated Warning Letter FDA Optimization of Warehouse and Distribution processes for prescription drugs and record keeping processes Strategic pricing and portfolio distribution for east ... - Mar 30
... Developed compliance quality systems and operations systems remediated Warning Letter FDA Optimization of Warehouse and Distribution processes for prescription drugs and record keeping processes Strategic pricing and portfolio distribution for east ... - Mar 30
Inside sales, operations manager and vendor relations
Elk Grove Village, IL
... Crystal Reporting • Oversaw operations of purchasing • Primary contact with shipping vendors • Executed overseas tariff and FDA forms • Customer service relating to order attainment, tracking and follow-up Global MRO Products, Rolling Meadows, Il, ... - Mar 30
... Crystal Reporting • Oversaw operations of purchasing • Primary contact with shipping vendors • Executed overseas tariff and FDA forms • Customer service relating to order attainment, tracking and follow-up Global MRO Products, Rolling Meadows, Il, ... - Mar 30