| Resume alert | Resumes 1 - 10 of 530 |
R D Clinical Operations
Basking Ridge, NJ
... making and accelerate clinical trial recruitment by 25% Associate Director, Global R&D, Antibiotic Support, Doribax, 2013 – 2014 ●Appointed to rotational position to oversee the global divestiture of Doribax, an antibiotic for serious infections; ... - Jun 20
... making and accelerate clinical trial recruitment by 25% Associate Director, Global R&D, Antibiotic Support, Doribax, 2013 – 2014 ●Appointed to rotational position to oversee the global divestiture of Doribax, an antibiotic for serious infections; ... - Jun 20
Financial Services Risk Management
South River, NJ
... Reduced complex, large query 30TB+ scientific and clinical trial data sets for complex Real World Evidence queries from structured and unstructured data on Cloudera data lakes. Integrated clinical data using EPIC EHR/EMR with payer and provider ... - Jun 19
... Reduced complex, large query 30TB+ scientific and clinical trial data sets for complex Real World Evidence queries from structured and unstructured data on Cloudera data lakes. Integrated clinical data using EPIC EHR/EMR with payer and provider ... - Jun 19
Executive Assistant Legal
Morristown, NJ
Tracy Valerio Rockaway, New Jersey ***** Phone:973-***-**** Email:ad6ilk@r.postjobfree.com WORK EXPERIENCE Tango, Dickinson, Lorenzo, McDermott and McGee, LP Legal Assistant, Premise Liability Defense November 2015-Present Trial calendar management ... - Jun 17
Tracy Valerio Rockaway, New Jersey ***** Phone:973-***-**** Email:ad6ilk@r.postjobfree.com WORK EXPERIENCE Tango, Dickinson, Lorenzo, McDermott and McGee, LP Legal Assistant, Premise Liability Defense November 2015-Present Trial calendar management ... - Jun 17
Service Representative Customer
Edison, NJ
... Expertise in aforementioned areas of more than 10 years, for both clinical trial products and post marketed vaccines, drugs/Medical Devices. In depth knowledge of US FDA, GxP areas including (cGMP, GCLP, and GCP), ICH, GvP, and EU PV regulations to ... - Jun 11
... Expertise in aforementioned areas of more than 10 years, for both clinical trial products and post marketed vaccines, drugs/Medical Devices. In depth knowledge of US FDA, GxP areas including (cGMP, GCLP, and GCP), ICH, GvP, and EU PV regulations to ... - Jun 11
Clinical Operations Management
North Brunswick, NJ
... P&L, project planning and resource management, regulatory services, training, business process and clinical development improvement, device and drug clinical trial management, medical device approvals, and quality assurance including SOP management. ... - Jun 02
... P&L, project planning and resource management, regulatory services, training, business process and clinical development improvement, device and drug clinical trial management, medical device approvals, and quality assurance including SOP management. ... - Jun 02
Data Quality Business Analyst
West Orange, NJ, 07052
... EXPERIENCE Vertex Pharmaceuticals/ Business Analyst/System Validation Management 7/22 - present Working with business users and vendors to gather requirements and develop BRD for clinical trial data CRF and reporting. Defined testing criteria and ... - May 26
... EXPERIENCE Vertex Pharmaceuticals/ Business Analyst/System Validation Management 7/22 - present Working with business users and vendors to gather requirements and develop BRD for clinical trial data CRF and reporting. Defined testing criteria and ... - May 26
Risk Management Case
Washington, NJ
... Reviews (Ten Years Experience) oCase/Disease Management oCare Coordination • Regulatory: oTrained by civil trial attorneys on medical malpractice Laws and medical chart review for causation in National and State (NY & NJ) Malpractice law. ... - May 26
... Reviews (Ten Years Experience) oCase/Disease Management oCare Coordination • Regulatory: oTrained by civil trial attorneys on medical malpractice Laws and medical chart review for causation in National and State (NY & NJ) Malpractice law. ... - May 26
Clinical Research Trial
Ringoes, NJ, 08551
... Competencies including: ●ICH GCP E6 R (2) ●FDA Regulations 21CFR 11, 50, 54, 56 and the Common Rule 45CFR46 ●Data Management ●Informed Consent Process ●Clinical Trial Operations from feasibility through close-out ●GDP following ALCOA-C principles. ... - May 21
... Competencies including: ●ICH GCP E6 R (2) ●FDA Regulations 21CFR 11, 50, 54, 56 and the Common Rule 45CFR46 ●Data Management ●Informed Consent Process ●Clinical Trial Operations from feasibility through close-out ●GDP following ALCOA-C principles. ... - May 21
Executive Director United States
Morristown, NJ
... Law Association for Crimes Across History (LACAH), June 2020 - June 2022 Organized and managed monthly mock trial tournaments online with students from both the U.S. Teams and International Teams such as China, Coached the U.S. Team in mock trial ... - May 21
... Law Association for Crimes Across History (LACAH), June 2020 - June 2022 Organized and managed monthly mock trial tournaments online with students from both the U.S. Teams and International Teams such as China, Coached the U.S. Team in mock trial ... - May 21
Software Development Management Process
Edison, NJ
... Supporting Clinical and Regulatory users managing regulatory binders, submissions, and electronic Trial Master Files (eTMFs). • Website Deployment– Spearheaded LifebankUSA website and integration projects that required website hosting with an ... - May 13
... Supporting Clinical and Regulatory users managing regulatory binders, submissions, and electronic Trial Master Files (eTMFs). • Website Deployment– Spearheaded LifebankUSA website and integration projects that required website hosting with an ... - May 13