Brandy Bryant Email & Phone Number

United States

Denver, Colorado, Us

Oversaw and supervised a multitude of clinical research trials ranging from Phase 2 to Phase 4 in a wide variety of therapeutic areas. Well-versed in all aspects of a clinical trial from start-up to close-out. Collaborated on SOP development and AAHRP certification.

Managed daily operations, studies and study teams responsible for clinical research activities. Provided support and direction for clinical research personnel. Involved in hiring selection and training of staff. Ensured adherence of Good Clinical Practice and accurate data collection and reporting.

Albuquerque, New Mexico, Us

Principal Duties:• Facilitate and coordinate daily clinical trial activities from start up through the end of the trial• Schedule and conduct study participant appointments and serve as the patient liaison to the PI and other participating physicians• Implement protocol including study procedures and timelines, inclusion and exclusion criteria, confidentiality and privacy protections• Collaborate with the Principal Investigator, perform Informed consent process by communicating clearly and appropriately with potential study subjects• Develop clinical study budgets based on proposed study protocols. Track study budget, invoices and payments• Coordinate approval of new study agreements and contracts• Coordinate and attend sponsor prequalification visits, monitor visits, and close out visits• Maintain trial source documents; design and revision• Complete case report forms per written guidelines. Respond to sponsor queries and perform query resolution. Report and document all AE’s and SAE’s with follow up• Coordinate with PI and department to help ensure that clinical research and related activities are performed in accordance with Federal regulations and sponsoring agency policies and procedures• Prepares and review documents submitted to IRB• Assist the PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of studies. Help to design and implement SOP’s. Maintains records and other documentation of training• Screening and recruitment of subjects along with subject retention• Ensures that all materials for each clinical trial are readily available• Performs specimen collection, processing and shipping of biological substances• Maintains Investigational product accountability and ensures IP is maintained in secure, climate controlled conditions

Albuquerque, New Mexico, Us

I took pride in my work as a Certified Medical Assistant and always strived to provide the best support for my patient's and provider's. Patient's were always roomed in a timely manner with all information up to date and ready for the provider. I am proficient in Prior Authorizations, Phlebotomy, Lab Processing, Referrals, and all the basic medical assistant duties. I was a leader amongst my peers and was always there to help other's.

Associate'S Degree, Health Services/Allied Health/Health Sciences, General

Medical Assistant, Medical/Clinical Assistant