| Resume alert | Resumes 1 - 10 of 391 |
Data Entry Front Desk
Raleigh, NC
... duties of a clinical and developmental nature in support of multi-center clinical trials to ensure adherence to protocol, FDA, and international guidelines, and to ensure the quality of data received during the start up and maintenance phases of ... - Apr 11
... duties of a clinical and developmental nature in support of multi-center clinical trials to ensure adherence to protocol, FDA, and international guidelines, and to ensure the quality of data received during the start up and maintenance phases of ... - Apr 11
Creative Project Manager
Central Park, NC, 27701
... 2019 Whole Foods Market, Chapel Hill, NC — Signage Auditor - Produce Department ● Organic audits & adherence according to FDA standards, receiving, new hire & cross-team training 2019 - Present TG Floristry, Raleigh, NC — Consultant + Contractor ● ... - Apr 11
... 2019 Whole Foods Market, Chapel Hill, NC — Signage Auditor - Produce Department ● Organic audits & adherence according to FDA standards, receiving, new hire & cross-team training 2019 - Present TG Floristry, Raleigh, NC — Consultant + Contractor ● ... - Apr 11
Clinical Operations Project Manager
Garner, NC
... ·Obtained project information, analyzed data, and prepared documents for FDA regulatory submissions. ·Reviewed protocol documentation according to regulatory compliance in preparation for audit review. ·Created work instructions guide and trained ... - Apr 04
... ·Obtained project information, analyzed data, and prepared documents for FDA regulatory submissions. ·Reviewed protocol documentation according to regulatory compliance in preparation for audit review. ·Created work instructions guide and trained ... - Apr 04
Clinical Research Project Manager
Research Triangle Park, NC, 27709
... Sponsors and Institutional Review Board (IRB) • Prepared and processed all regulatory documentation through the IRB, CTSRMC, FDA for Abbvie pre-start up study and study delivery timelines SOPs • Prepared and processed all required regulatory ... - Mar 24
... Sponsors and Institutional Review Board (IRB) • Prepared and processed all regulatory documentation through the IRB, CTSRMC, FDA for Abbvie pre-start up study and study delivery timelines SOPs • Prepared and processed all required regulatory ... - Mar 24
Us Citizen Process Engineering
Cary, NC
... Regulatory Experience GLP, GMP, USP, FDA Natural products Purifying of any ingredients by the means of various techniques, such as extractions, filtrations, centrifugations, chromatographic and so on. Structure identification and characterization. ... - Mar 23
... Regulatory Experience GLP, GMP, USP, FDA Natural products Purifying of any ingredients by the means of various techniques, such as extractions, filtrations, centrifugations, chromatographic and so on. Structure identification and characterization. ... - Mar 23
Risk Management Operational
Raleigh, NC
... Drug Safety Alliance, Raleigh, NC 11/2014 – 06/2015 Contract HR Specialist (Contract Completed) Conducted extensive internal record audits to analyze FDA compliance metrics, aligning organizational goals with strategic plan. Assured that vendor ... - Mar 18
... Drug Safety Alliance, Raleigh, NC 11/2014 – 06/2015 Contract HR Specialist (Contract Completed) Conducted extensive internal record audits to analyze FDA compliance metrics, aligning organizational goals with strategic plan. Assured that vendor ... - Mar 18
Forklift Operator Supply Chain
Henderson, NC
... Plant Service Attendant Debbies' Staffing @Santa Fe Tobacco - Oxford, NC May 2012 to August 2017 Meets the fda, osha, regulation's. clean and blend tobacco. Make sure proper weight and samples are taken. Driver CDL B Presidental Tree service LLC - ... - Feb 27
... Plant Service Attendant Debbies' Staffing @Santa Fe Tobacco - Oxford, NC May 2012 to August 2017 Meets the fda, osha, regulation's. clean and blend tobacco. Make sure proper weight and samples are taken. Driver CDL B Presidental Tree service LLC - ... - Feb 27
Customer Service, Clinical Research, Trial Master File Specialist
Durham, NC
... of essential study and program documents Direct communication with CRO teams and third-party vendors Review new and revised FDA 1572s ICF review Records and compiles minutes from study team meetings Updates and maintains tracking logs FHI 360 Durham ... - Feb 22
... of essential study and program documents Direct communication with CRO teams and third-party vendors Review new and revised FDA 1572s ICF review Records and compiles minutes from study team meetings Updates and maintains tracking logs FHI 360 Durham ... - Feb 22
Social Media Customer Service
Raleigh, NC
... units Duke Clinical Research Institute (DCRI), Durham, NC March 2017 – July 2017 Contracted Clinical Trials Associate II // Duke Box Committee Member Managed the closing of long-term paper studies, including final QC before FDA and client ... - Feb 21
... units Duke Clinical Research Institute (DCRI), Durham, NC March 2017 – July 2017 Contracted Clinical Trials Associate II // Duke Box Committee Member Managed the closing of long-term paper studies, including final QC before FDA and client ... - Feb 21
Behavioral Health Medical Claims
Durham, NC
... • CME Editor & Accreditation • Dynamic Leadership • Pharmaceutical Sales • Behavioral Health • Research • Publications • FDA Regulations • HIPAA • People Operations • Training & Mentoring KEY ACCOMPLISHMENTS • Successful Clinical Project Outcomes ... - Feb 06
... • CME Editor & Accreditation • Dynamic Leadership • Pharmaceutical Sales • Behavioral Health • Research • Publications • FDA Regulations • HIPAA • People Operations • Training & Mentoring KEY ACCOMPLISHMENTS • Successful Clinical Project Outcomes ... - Feb 06