A company is looking for a Senior Clinical Research Associate responsible for monitoring clinical trials and ensuring compliance with regulatory standards.
Key ResponsibilitiesConduct site monitoring visits and ensure adherence to Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesManage the progress of assigned studies, including tracking regulatory submissions, recruitment, and data managementMentor clinical staff and collaborate with study team members for project execution supportRequired QualificationsBachelor's Degree in a scientific discipline or health care preferredAt least 4 years of on-site monitoring experienceIn-depth knowledge of clinical research regulatory requirements, including GCP and ICH guidelinesProficiency in Microsoft Word, Excel, and PowerPointStrong therapeutic and protocol knowledge as provided in company training
Senior Clinical Research Associate
A company is looking for a Senior Clinical Research Associate responsible for monitoring clinical trials and ensuring compliance with regulatory standards. ...
Senior Clinical Research Coordinator
The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as doc. ...
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A company is looking for a Senior Clinical Data Associate - Risk-Based Quality Monitoring (RBQM). ...
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Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
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As a Senior Associate, you'll work as part of a team of problem solvers, helping to solve complex business issues from strategy to execution. Working knowledge of the tax issues associated with Research and Development. Proficient technical skills with research credit regulations from the IRS, resea...
Senior Clinical Research Coordinator
EKG, blood collection)Processing all samples and shipping to Central LabMaintaining study sourceEntering data into sponsor EDC and query resolution as the sole Senior Clinical Research Coordinator (SCRC) on-site, the chosen candidate must be adept at protocol comprehension and be capable of working ...
Senior Project Manager / Associate Director, Project Management - Metabolic Disease (Obesity/T2 Diabetes/CV) - US or Canada Remote Based
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Associate Director, Project Management. Senior P...
Senior Clinical Research Coordinator
The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials. CRC applies critical thinking and crea...