Shilburg Research
Shilburg Research
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Clinical Trial & Regulatory Affairs Services

Clinical Trial & Regulatory Affairs ServicesClinical Trial & Regulatory Affairs ServicesClinical Trial & Regulatory Affairs Services
Contact Us

Clinical Trial & Regulatory Affairs Services

Clinical Trial & Regulatory Affairs ServicesClinical Trial & Regulatory Affairs ServicesClinical Trial & Regulatory Affairs Services
Contact Us

Welcome

For nearly two decades, Shondolyn Richburg has been a results oriented clinical research professional with experience in academia, private practice, pharmaceutical, and device industries.  Shondolyn is an active member of the Academy of Clinical Research Professionals (ACRP). She became a certified coordinator in 2008.

Services Offered

Staff training & education

Staff training & education

Staff training & education

Audit prep

Staff training & education

Staff training & education

.

SOP development

Staff training & education

Clinical trial monitoring

Clinical trial monitoring

Creation of clinical trial assistive documents

Clinical trial monitoring

Data capture templates development

Creation of clinical trial assistive documents

Creation of clinical trial assistive documents

.

Creation of clinical trial assistive documents

Creation of clinical trial assistive documents

Creation of clinical trial assistive documents

Site prep for clinical trials initiation

Clinical trials contract and budget development

Site prep for clinical trials initiation

Local and central regulatory support

Clinical trials contract and budget development

Site prep for clinical trials initiation

Clinical trials contract and budget development

Clinical trials contract and budget development

Clinical trials contract and budget development

Shondolyn's passions are providing patients with seamless transitions from standard of care to clinical trials, mentoring less experienced personnel, and building multidisciplinary relationships. These motivations propelled her to start Shilburg Research LLC.


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