Working knowledge of FDA regulations and ICH guidelines to ensure compliance with both during clinical trial conduct. Ensure studies are carried out according to the study protocol, SOPs, and ICH/GCP ...
These activities include supporting the Clinical Trial Manager (CTM) with the creation of the TMF ... Associate or bachelor's degree or relevant experience in a health-related field, five or more years ...
REGIONAL CLINICAL RESEARCH ASSOCIATE The requirements listed below under the job title are ... Proficiency with electronic data capture and electronic Trial Master File. Proven ability to ...
We are about to start a Phase 2 trial in patients with amyotrophic lateral sclerosis ("ALS"). In ... The Senior Regional Clinical Research Associate (SRCRA) will report directly to the Senior Regional ...
Clinical Trial Manager, Clinical Pharmacology (Contract) Function: Clinical Operations Location: Remote Position Summary: Work with a sponsor biotech who conducts discovery research, clinical ...
Under direct supervision, the Clinical Research Associate will serve as a clinical trial site manager, junior project manager, and will provide the clinical research department with support for ...
... Trial Master File (TMF) documents are compliant with Good Documentation Practices, Edwards internal SOPs, and US and OUS regulations (15%) * Assess current processes, identify opportunities, and ...
Senior Clinical Trial Manager Contractor- CNS (6 Month Contract Position / Eligible for renewal/possible conversion) The biotech dedicated to developing breakthrough therapies for neurodegenerative ...