Clinical Scientist, you will work with the clinicalresearch team in aiding in the development of clinical... clinicalresearch team in the development of clinical..
Clinical Scientist with Hepatology experience. The Contract Clinical Scientist will work with the clinicalresearch team, aiding in the development of clinical..
Investigator Meetings
- Working with clinical scientists and Clinical Data Management to set-up database... years in pharma clinicalresearch
- Experience with..
clinical development knowledge, regulatory compliance knowledge, Hepatolgy knowledge, and protocol design and execution abilities
-3+ years ClinicalResearch..
Participating as lead clinical representative on... training and board certification
-3+ years ClinicalResearch Industry experience in CNS, preferably in..
pipeline of ongoing research and a number of mission-critical projects.
Current critical projects include:
- Submission of clinical trials data to FDA..
in clinicalresearch and are seeking experienced research professionals for upcoming ClinicalResearch... from ClinicalResearch Physician and senior clinical..
At Kforce ClinicalResearch, we don't just offer jobs... is currently seeking a Clinical Data Manager in Bridgewater, NJ. The Clinical Data Manager will contribute..
& Outcomes Research
Morris County, NJ
Job Summary:
Director, Health Economics & Outcomes Research is... & outcomes research, including specific clinical..
At Kforce ClinicalResearch, we don't just offer jobs... Oracle Clinical studies in conjunction with the Oracle Clinical developers, clinical data coordinators..
Job Description Scientific leader serving as mentor, overseeing training of Novo Nordisk CPR clinicians involved in early development projects including Princeton IMOs and clinical pharmacologists. Interface with NNA/S clinical development to facilit
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Description Liaison with drug discovery and clinicalresearch colleagues for compound selection and immunology drug development decision making. Analysis and interpretation of clinical study data, including safety and pharmacological endpoints. Devel
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Summary: The incumbent will be responsible for the overall management and implementation of global clinicalresearch studies for the investigation of new drugs. Drug product candidates under investigation may belong to any therapeutic area. The incum
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