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 Associate -3 month assignment IC Preferred- Central Region
A growing and exciting biotech company specializing in central nervous system (CNS) diseases are hiring for a Senior Clinical Research Associate (SCRA). ...
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A company is looking for a Clinical Research Associate - Oncology. ...
Specialized Tax Services - Research & Development - Senior Associate
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...
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As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Contribute to the identification of new sites for clinical trials; analyse capability and support CRMA and CSM in making recommendation for trial inclusion. Abili...
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Excellent written and oral communication skills and a demonstrated ability to interact with junior and senior team members, senior management and other stakeholders or professionals;. Position at Berkeley Research Group, LLC The BRG Transaction Advisory practice is seeking to add professionals due t...
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Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. ...
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Manages clinical research studies and adheres to Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), study protocols, clinical trial agreements, and regulations governing clinical research. Coordinate research participant visits and study-related procedures according to study proto...