Clinical Trial Data Management Jobs in Livingston, AL
Pharmaceutical Research Associates, Inc - Emelle, Alabama
knowledge of Coding to accomplish tasks May provide formal guidance to less experienced team members Supporting clinical trial data management function in a growing team Fully remote based role working 3pm
Register your RESUMEfrom: resume-library.com - 3 days ago
Pharmaceutical Research Associates, Inc - Emelle, Alabama
, applicable regulations, and SOPs. Manages the investigative site staff to facilitate trial deliverables, e.g., subject enrollment, data deliverables. Verifies proper management and accountability
Register your RESUMEfrom: resume-library.com - 8 days ago
Pharmaceutical Research Associates, Inc - Emelle, Alabama
, applicable regulations, and SOPs. Manages the investigative site staff to facilitate trial deliverables, e.g., subject enrollment, data deliverables. Verifies proper management and accountability
Register your RESUMEfrom: resume-library.com - 11 days ago
Pharmaceutical Research Associates, Inc - Emelle, Alabama
applications, Clinical Trial Management Systems, IVRS/IWRS and Electronic Data Capture platforms Mentors CRAs new to the position or company Serves as an observation visit leader Conducts monitoring evaluation
Register your RESUMEfrom: resume-library.com - 17 days ago
Pharmaceutical Research Associates, Inc - Emelle, Alabama
applications, Clinical Trial Management Systems, IVRS/IWRS and Electronic Data Capture platforms Mentors CRAs new to the position or company Serves as an observation visit leader Conducts monitoring evaluation
Register your RESUMEfrom: resume-library.com - 17 days ago
Pharmaceutical Research Associates, Inc - Emelle, Alabama
/ patients organizations and key contact point for these throughout the study. Interact/train new investigators to work on clinical trials. Attend key therapeutic trainings/meetings and/or industry trainings
Register your RESUMEfrom: resume-library.com - 18 days ago
Pharmaceutical Research Associates, Inc - Emelle, Alabama
, Engineering, Life Science, or related discipline with 8+ (9+) years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry
Register your RESUMEfrom: resume-library.com - 26 days ago
Pharmaceutical Research Associates, Inc - Emelle, Alabama
and Conformance of Clinical Trial data to the NCDS Standards. Manage the Load, Transfer and Conformance of Clinical Trial data to the NCDS Standards. For assigned Clinical trials initiate data load from OC/RDC
Register your RESUMEfrom: resume-library.com - 27 days ago
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