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The Central Monitor (CM) will perform centralized and prompt monitoring activities for Phase I-IV clinical research and/or non-interventional studies (NIS) in accordance with project plans, the protocol, ICH-GCP, and/or all applicable local and federal regulatory requirements as well as ensure patient safety and data integrity using a variety of statistical and analytical tools. The CM will analyze site and study level data in the applicable data analytics tool(s) and may identify risks and trends at the site and study level, as well as operational performance issues. The CM shall summarize the analysis, provide recommendations, and share with the project team as appropriate for operational considerations/actions. The CM performs all tasks routinely and independently with minimal oversight per Alimentiv policies, SOPs, Work Instructions, and guidance documents, and in line with the study monitoring plans. May provide support to other CMs including training and mentoring.
\nProject Support
*Accommodations for job applicants with disabilities are available upon request
#LI-Remote
Full Time
Scientific Services
$65k-90k (estimate)
02/03/2024
04/03/2024
alimentiv.com
SAN DIEGO, CA
<25
1986
DENISE STARK
<$5M
Scientific Services
From 1986 to 2020 we operated as Robarts Clinical Trials and built a strong foundation in the medical research community. In 2020, we became Alimentiv but retained our commitment to clinical trials, medical imaging, and precision medicine for GI-related ailments.