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Sara M. is listed as Senior Clinical Trial Lead at Fortrea, based in Salt Lake City, Utah, United States. AeroLeads shows a work email signal at covance.com and a matched LinkedIn profile for Sara M..
Sara M. previously worked as Clinical Trial Lead at Labcorp Drug Development and Senior Clinical Reseach Associate II at Labcorp Drug Development. Sara M. holds Bachelor Of Science, Psychology- Behavioral from Weber State University.
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AeroLeads found 1 current-domain work email signal for Sara M.. Compare company email patterns before reaching out.
I am passionate about the clinical research industry. Starting in college with Pediatrics and the Emergency Department as a Clinical Assistant, I have 20+ years in this industry including Regulatory Affairs, Project Management, Clinical Monitoring and Clinical Operations. I utilize my vast knowledge and leadership skills to bring teams together and deliver projects to client specifications.
Listed skills include Clinical Research, Edc, Gcp, Research, and 46 others.
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Durham, North Carolina, Us
Management of clinical project team across client portfolio of studies including project metrics, timelines, conduct, resourcing, and training to achieve successful delivery of clinical activities by meeting internal and external client requirements.
Burlington, North Carolina, Us
Managed clinical project team across client portfolio of studies including project metrics, timelines, conduct, resourcing, and training to achieve successful delivery of clinical activities by meeting internal and external client requirements.
Burlington, North Carolina, Us
Managed, led, motivated, and supported as defined group of direct report CRAs as well as the CRA project teams for assigned projects.
Burlington, North Carolina, Us
Coordinated and performed comprehensive site management for Phase II-IV clinical trials.
Burlington, North Carolina, Us
Coordinated and performed comprehensive site management for Phase II-IV clinical trials.
Salt Lake City, Us
Coordinated and performed comprehensive site management for Phase II-IV clinical trials.
Salt Lake City, Us
Responsible for ensuring that all requirements for collecting, filing, and storing study-related documents and records are fulfilled according to good clinical practice (GCP) and applicable regulations. Maintain complete, current, and accurate study and site files. Perform accurate audits of sites, project files, and data collection, as well as reparation. Prepare and submit study submissions to the IRB as well as ensure completion of interim and other reports. Maintain primary contact with appropriate IRB members in relation to the study. Handle any other IRB related issue. Provide project support to the project manager.
Salt Lake City, Us
Managed projects and personnel that serve in support of projects by providing direct oversight on the following: draft protocols, assist with the design of necessary documents for the studies, instruct and train necessary site personnel, collect, analyze, and record clinical data, prepare necessary reports, coordinate clinical trial activities with internal and external personnel, conduct trial initiation, interim and close-out visits, monitor site performance and compliance and provide management with necessary reports, updates and recommendations, interact with all internal and external personnel involved with study and travel to sites as required. Served as primary contact person with the sponsor regarding the study.
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Sara M. works for Fortrea.
Sara M. is listed as Senior Clinical Trial Lead at Fortrea.
AeroLeads has found 1 work email signal at @covance.com for Sara M. at Fortrea.
Sara M. is based in Salt Lake City, Utah, United States while working with Fortrea.
Sara M. has worked for Fortrea, Labcorp Drug Development, and Pegus Research.
You can use AeroLeads to view verified contact signals for Sara M. at Fortrea, including work email, phone, and LinkedIn data when available.
Sara M. holds Bachelor Of Science, Psychology- Behavioral from Weber State University.
Sara M. is listed with skills including Clinical Research, Edc, Gcp, Research, Irb, Clinical Trials, Cro, and Regulatory Affairs.
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