| Resume alert | Resumes 41 - 50 of 1579 |
Sql Server Database Administrator
Ashburn, VA
... Working as a Principal DBA for BITS on CEDR applications (CDP-Corporate Database Portal, CI-Clinical Investigator Site Selection, PVC-Pharmacovigilance Compliance Site Selection and IRB SST - Institutional Review Board Site Selection Tool). The ... - Mar 14
... Working as a Principal DBA for BITS on CEDR applications (CDP-Corporate Database Portal, CI-Clinical Investigator Site Selection, PVC-Pharmacovigilance Compliance Site Selection and IRB SST - Institutional Review Board Site Selection Tool). The ... - Mar 14
Medical Records/HIPAA/Data visualization/Tableau/Power BI/SQL
Bridgeport, CT
... Monitoring Adverse-drug events & reporting to institutional database and Pharmacovigilance. Consulted on dosages, medication substances etc. Advised on the correct administration of drugs. Assessed the results of pharmaceutical treatments. ... - Mar 13
... Monitoring Adverse-drug events & reporting to institutional database and Pharmacovigilance. Consulted on dosages, medication substances etc. Advised on the correct administration of drugs. Assessed the results of pharmaceutical treatments. ... - Mar 13
Pharmacy Technician Medical Equipment
Queens, NY
... - Expires Aug 2024 Skills Medication Therapy Management (MTM) • Pharmacy Practice • Pharmaceutical Sales • Teamwork • Leadership • New Business Development • Compounding • Pharmaceutical Industry • Marketing • Pharmacovigilance Dabeer Hasan - page 2 - Mar 12
... - Expires Aug 2024 Skills Medication Therapy Management (MTM) • Pharmacy Practice • Pharmaceutical Sales • Teamwork • Leadership • New Business Development • Compounding • Pharmaceutical Industry • Marketing • Pharmacovigilance Dabeer Hasan - page 2 - Mar 12
United States Clinical Research
San Diego, CA
... Assessed factors that might affect subject’s safety and clinical data integrity at an investigator site such as protocol deviation/violations and pharmacovigilance issues. • Assured all study staff who will conduct the study have received proper ... - Mar 10
... Assessed factors that might affect subject’s safety and clinical data integrity at an investigator site such as protocol deviation/violations and pharmacovigilance issues. • Assured all study staff who will conduct the study have received proper ... - Mar 10
Pharmacy Technician Prior Authorization
Warren, NJ
... Pharmacology, Pharmacovigilance (Drug Safety), PMQA, MDR, 21 CFR Part 11. 21 CFR Part 210, 211 & 820. MeDRA, Medwatch, 510(k) & PMA, WHODD, CAPA, GxP, cGMP, Medical Billing and Coding. Medical Records Review, Claims Analyst. Experience 10/2023 - ... - Mar 10
... Pharmacology, Pharmacovigilance (Drug Safety), PMQA, MDR, 21 CFR Part 11. 21 CFR Part 210, 211 & 820. MeDRA, Medwatch, 510(k) & PMA, WHODD, CAPA, GxP, cGMP, Medical Billing and Coding. Medical Records Review, Claims Analyst. Experience 10/2023 - ... - Mar 10
Pharmaceutical SME RE: PV., Clinical research, Medical monitoring
Schwenksville, PA
... PROPHARMA GROUP, Fort Washington, PA Nov-2020-Dec-2021 Senior Clinical Pharmacovigilance Specialist ·Manages individual case safety reports (serious adverse events, adverse events of interest and reports of pregnancy) through intake, documentation ... - Mar 09
... PROPHARMA GROUP, Fort Washington, PA Nov-2020-Dec-2021 Senior Clinical Pharmacovigilance Specialist ·Manages individual case safety reports (serious adverse events, adverse events of interest and reports of pregnancy) through intake, documentation ... - Mar 09
Organizational Development Project Management
Sandyston, NJ, 07826
... Proposed and implemented a Drug Safety (Pharmacovigilance) compliance training program to reduce the redundancies and the number of trainings from 40 into one program resulting in the training reduction time from 65 hours to 1 hour. Design, ... - Mar 07
... Proposed and implemented a Drug Safety (Pharmacovigilance) compliance training program to reduce the redundancies and the number of trainings from 40 into one program resulting in the training reduction time from 65 hours to 1 hour. Design, ... - Mar 07
Data Entry Patient Care
Dallas, TX
... Operating Procedures (SOPs), and training materials Expertise in medical coding using MedDRA and handling dechallenge and rechallenge scenarios Comprehensive knowledge on clinical trials (Phase I-IV), pharmacovigilance principles and regulations. ... - Mar 06
... Operating Procedures (SOPs), and training materials Expertise in medical coding using MedDRA and handling dechallenge and rechallenge scenarios Comprehensive knowledge on clinical trials (Phase I-IV), pharmacovigilance principles and regulations. ... - Mar 06
Clinical drug trials, pharmacovigilance, certified in human research
Edison, NJ, 08817
... ad35zc@r.postjobfree.com LinkedIn: www.linkedin.com/in/lisa-latham-b4479478 732-***-**** Morganville, NJ Pharmacovigilance Summary Resilient, self-motivated drug safety professional dedicated for over sixteen years to pharmaceutical safety and ... - Mar 06
... ad35zc@r.postjobfree.com LinkedIn: www.linkedin.com/in/lisa-latham-b4479478 732-***-**** Morganville, NJ Pharmacovigilance Summary Resilient, self-motivated drug safety professional dedicated for over sixteen years to pharmaceutical safety and ... - Mar 06
Medical Director Tampa Fl
Wesley Chapel, FL
... the merger of both organizations(Bayer and Shering AG) (medical advisors for each of the divisions and product groups, Pharmacovigilance Country Head, Clinical Trial Manager, Training manager and Field Trainers) CV evaluation, interviews, selection, ... - Feb 29
... the merger of both organizations(Bayer and Shering AG) (medical advisors for each of the divisions and product groups, Pharmacovigilance Country Head, Clinical Trial Manager, Training manager and Field Trainers) CV evaluation, interviews, selection, ... - Feb 29