| Resume alert | Resumes 51 - 60 of 83 |
Program Manager
Randolph, NJ
... Functional and process oLifeSciences R&D: Global Clinical Operations, Clinical collaboration, Clinical Data Management, Pharmacovigilance oGxP, CSV, 21CFR Part11 oSales and Marketing: SalesWorkBench, Price Analytics, Marketing Resource Management ... - 2016 Jan 07
... Functional and process oLifeSciences R&D: Global Clinical Operations, Clinical collaboration, Clinical Data Management, Pharmacovigilance oGxP, CSV, 21CFR Part11 oSales and Marketing: SalesWorkBench, Price Analytics, Marketing Resource Management ... - 2016 Jan 07
Manufacturing Six Sigma
Piscataway Township, NJ
... Understanding of Validation Development Lifecycle, Process and Cleaning Validation, Computer system validation, Risk analysis by FMEA, DOE (Design of Experiment), Audit Trail, pharmacovigilance. ACTIVITIES INTERPHEX – 2010-2011 IPC – 60th “Indian ... - 2015 Jul 06
... Understanding of Validation Development Lifecycle, Process and Cleaning Validation, Computer system validation, Risk analysis by FMEA, DOE (Design of Experiment), Audit Trail, pharmacovigilance. ACTIVITIES INTERPHEX – 2010-2011 IPC – 60th “Indian ... - 2015 Jul 06
Management Customer Service
Raritan, NJ
... Manage monthly data updates to Pharmacovigilance System Master File (PSMF) via close interaction with Regulatory, Aggregate and Safety Management team. . Provide Health Authority Request update submitted by Safety Management team on monthly metrics. ... - 2015 Apr 08
... Manage monthly data updates to Pharmacovigilance System Master File (PSMF) via close interaction with Regulatory, Aggregate and Safety Management team. . Provide Health Authority Request update submitted by Safety Management team on monthly metrics. ... - 2015 Apr 08
Project Manager Management
Gillette, NJ, 07933
... BUSINESS SKILLS: Extensive knowledge of Research & Development, Drug Discovery, Drug Safety, Drug Development, Regulatory, Pharmacovigilance, IT SAS Drug Development, Regulatory Submissions (PSURS), Clinical Trials, Quality Assurance, Manufacturing ... - 2015 Feb 27
... BUSINESS SKILLS: Extensive knowledge of Research & Development, Drug Discovery, Drug Safety, Drug Development, Regulatory, Pharmacovigilance, IT SAS Drug Development, Regulatory Submissions (PSURS), Clinical Trials, Quality Assurance, Manufacturing ... - 2015 Feb 27
Medical Manager
Morristown, NJ
... *+ years of Medical Affairs experience in the Pharmaceutical Industry, including 6+ years of Medical Information and 3 years in Pharmacovigilance. . Excellent writing skills with expertise in writing medical narratives, narratives for periodic ... - 2014 Oct 24
... *+ years of Medical Affairs experience in the Pharmaceutical Industry, including 6+ years of Medical Information and 3 years in Pharmacovigilance. . Excellent writing skills with expertise in writing medical narratives, narratives for periodic ... - 2014 Oct 24
Customer Service Data Entry
Union, NJ
... 04/11 – 12/12 M erck, Springfield, NJ (contract assignment) Documentation Clerk • Handled Clinical Tr ial documents through management lifecycle from scanning, indexing and batching Global Pharmacovigilance (GPV). • Familiar with high level ... - 2014 Sep 23
... 04/11 – 12/12 M erck, Springfield, NJ (contract assignment) Documentation Clerk • Handled Clinical Tr ial documents through management lifecycle from scanning, indexing and batching Global Pharmacovigilance (GPV). • Familiar with high level ... - 2014 Sep 23
Administrative Assistant Customer Service
Edison, NJ
... Pharmacovigilance; Good Manufacturing/ Distribution practices Other Interests --Life Coaching: http://savina-cavallo.blogspot.com/ --Volunteering: youth mentor, women's counselor --Reading: self-development, professional growth - 2014 Aug 14
... Pharmacovigilance; Good Manufacturing/ Distribution practices Other Interests --Life Coaching: http://savina-cavallo.blogspot.com/ --Volunteering: youth mentor, women's counselor --Reading: self-development, professional growth - 2014 Aug 14
Medical Manager
Flanders, NJ
... • Expedited reporting of Serious Adverse Events (SAEs) from the investigator site, CRO and/or affiliates which were also submitted to pharmacovigilance department in accordance with ICH guidelines on Clinical Safety Data. • Contacted the SAE ... - 2014 Jul 21
... • Expedited reporting of Serious Adverse Events (SAEs) from the investigator site, CRO and/or affiliates which were also submitted to pharmacovigilance department in accordance with ICH guidelines on Clinical Safety Data. • Contacted the SAE ... - 2014 Jul 21
Customer Service High School
Piscataway Township, NJ
... Maintain an Excel database of Active Investigators for Post marketing Studies Reconcile Serious Adverse Events captured in the Global Clinical database with those captured in the Global Pharmacovigilance database. Submission of IND and NDA expedited ... - 2014 Jun 05
... Maintain an Excel database of Active Investigators for Post marketing Studies Reconcile Serious Adverse Events captured in the Global Clinical database with those captured in the Global Pharmacovigilance database. Submission of IND and NDA expedited ... - 2014 Jun 05
Pharmacist, drug safety / pharmacovigilance, medical information
Middlesex, NJ, 08859
... Ibrahim * ****** ****** Parlin, New Jersey 08859 917-***-**** acdxjv@r.postjobfree.com pharmacovigilance/drug safety Specialist I am a licensed pharmacist (Doctor of Pharmacy) with 2 years of industry experience in US and Global Pharmacovigilance. I ... - 2014 Apr 30
... Ibrahim * ****** ****** Parlin, New Jersey 08859 917-***-**** acdxjv@r.postjobfree.com pharmacovigilance/drug safety Specialist I am a licensed pharmacist (Doctor of Pharmacy) with 2 years of industry experience in US and Global Pharmacovigilance. I ... - 2014 Apr 30