FOR SUPPORT +1.4802664862
services
Clinical strategy and protocol development • Operational planning & project management • Investigator and coordinator training • Registry deployment • Specimen procurement solutions • Clinical data capture strategy • Research network development & site identification • Site qualification & selection, initiation, training and management • Proprietary specimen & data tracking tools linking consent status • Clinical monitoring plans and management • CRO services • Data management • Research administration • Contract development & negotiation • Risk anticipation and barrier mitigation • FDA audit assessment, preparation, conduct, and follow-up documentation • IRB document submissions & oversight • Policy and procedural drafting and implementation • Report writing • Presentations • Workflow efficiencies • Solution based data capture systems • Medical writing solutions • Gap analysis
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About us
Project Manager(s)
Average years of experience: 25
Regulatory Expert(s)
Average years of experience: 20
Clinical Research Associate (CRA)
Average years of experience: 20
Coverage Analysis Expert(s)
Average years of experience: 10
research attorney(s)
Average years of experience: 22
clinical operations manager(s)
Average years of experience: 15
publication coordinator
Average years of experience: 12
specimen logistics specialist
Average years of experience: 10
biostatistician
Average years of experience: 20
technology analyst
Average years of experience: 8
mobile health application specialist
Average years of experience: 2
rates
Initial consultation free of charge
Hourly rates available
Fee for project flat rates
Modular rates
We provide all clients an accurate budget for which they can plan accordingly
We offer rate flexibility based upon both client & project needs
Our goal is to minimize your consultation budget to ensure your investment is focused on outcomes
references available upon request
sheri sanders, mba, bsn, rn
Years of experience: 25
Position: President & CEO
Ms. Sanders established Sanders Biomedical Consulting Firm, LLC to provide research consulting services tailored to biotech entities (both small and large) and diagnostic companies. Her many years of clinical and research experience identified a unique and unmet need to service these industries while continuing her support to develop compliant research operations within private practices and large healthcare organizations and academic research institutes. She has developed robust pathways to solve requirements of both research scientists and healthcare providers; all while ensuring seamless workflows are in place to advance translational research, obtain product approvals and increase market share.
OUR MISSION
TO IMPROVE CLINICAL UTILIZATION OF GENOMIC BASED DIAGNOSTIC SERVICES AND PROVIDE A SUCCESSFUL RESEARCH STRATEGY.
In the genomic era, scientific development is rapidly outpacing the clinical knowledge at the bedside. We strive to help large and small diagnostic companies bridge this gap to develop a solid foundation of research compliance, operational procedures and transactional strategies so they can be successful. We work collaboratively to identify your needs, assess your research compliance program, outline organizational gaps and maximize value in your genomic data to promote product expansion.