| Resume alert | Resumes 11 - 20 of 417 |
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
Food Safety Quality Assurance
Raleigh, NC
... Skills • Proficient in Microsoft Word, PowerPoint, Outlook, and Excel • SAP Super User • Auditing (Internal/External)-BRC, FDA, SQF, FSSC 22000, ISO 9001, AIB, Organic, Halal, Gluten Free, Non-GMO • Lean Six Sigma Methodologies • Total Quality ... - Feb 04
... Skills • Proficient in Microsoft Word, PowerPoint, Outlook, and Excel • SAP Super User • Auditing (Internal/External)-BRC, FDA, SQF, FSSC 22000, ISO 9001, AIB, Organic, Halal, Gluten Free, Non-GMO • Lean Six Sigma Methodologies • Total Quality ... - Feb 04
Technology Director
Raleigh, NC, 27608
... Led the design, implementation, and service of a global SAP data center in a Food and Drug Administration (FDA) regulated environment. The team included project managers, planners, business analysts, technical writers, and system administrators, and ... - Jan 30
... Led the design, implementation, and service of a global SAP data center in a Food and Drug Administration (FDA) regulated environment. The team included project managers, planners, business analysts, technical writers, and system administrators, and ... - Jan 30
Maintenance Manager Team
Morrisville, NC
... Generated and maintained work orders in accordance with FDA regulations. Led daily meetings with the production department to minimize down time and increase production yields, and with the maintenance team to measure performance against KPI. ... - Jan 19
... Generated and maintained work orders in accordance with FDA regulations. Led daily meetings with the production department to minimize down time and increase production yields, and with the maintenance team to measure performance against KPI. ... - Jan 19
Clinical Research Operations
Raleigh, NC
... Attendance of Weekly meetings to guide team for FDA approval. Medtronic, Minneapolis, MN November 2022–July 2023 Senior Clinical Research Associate – Medical Devices (Contract) Served as lead clinical research associate, managing 9+ sites across the ... - Jan 19
... Attendance of Weekly meetings to guide team for FDA approval. Medtronic, Minneapolis, MN November 2022–July 2023 Senior Clinical Research Associate – Medical Devices (Contract) Served as lead clinical research associate, managing 9+ sites across the ... - Jan 19
Clinical Research Hr Manager
Chapel Hill, NC
... Submission of CIOMS (EU) and MedWatch (FDA) reports for specific clients. Rewriting OG’s, DEG’s and SOP as it pertains to the project. Review product labeling for inclusion of applicable data in MedWatch reports for Medical device studies. Identify ... - Jan 15
... Submission of CIOMS (EU) and MedWatch (FDA) reports for specific clients. Rewriting OG’s, DEG’s and SOP as it pertains to the project. Review product labeling for inclusion of applicable data in MedWatch reports for Medical device studies. Identify ... - Jan 15
Quality Assurance Supply Chain
Durham, NC
... consumer products company • Conducted interviews with stakeholders to understand internal processes and to propose relevant FDA compliant solutions • Strategize market access insights for the novel medical device by interpreting market access ... - Jan 11
... consumer products company • Conducted interviews with stakeholders to understand internal processes and to propose relevant FDA compliant solutions • Strategize market access insights for the novel medical device by interpreting market access ... - Jan 11
Prior Authorization Patient Care
Cary, NC
... Monitors FDA and manufacturer updates for material changes to drug inventory, including but not limited to, recalls, black box warnings, new drugs to the market and brand to generic change. Process pharmacy appeals, interpreting member and provider ... - 2023 Dec 15
... Monitors FDA and manufacturer updates for material changes to drug inventory, including but not limited to, recalls, black box warnings, new drugs to the market and brand to generic change. Process pharmacy appeals, interpreting member and provider ... - 2023 Dec 15