Brianne Peters Email & Phone Number

St Louis, Missouri, United States

Cross functionally supporting sales, client services and lab operations to create an enhanced and customized operational solution around sample logistics, phlebotomy and connectivity for our Customers.

Wisconsin, United States

Support business development to articulate how EmVenio’s global DCT site, home and virtual visit capabilities can help improve trial patient experiences, diversity, recruitment, and retention. Provide operational leadership and DCT subject matter expertise during protocol development or interpretation of existing protocols to define the trial DCT site, recruitment, and follow-up strategy. Identify innovations to improve patient DCT trial access and experience while reducing the burden of trial participation. Define the department and build the DCT strategy team in line with the business demand and growth.

Los Angeles, California, United States

Responsible for the global development, operations oversight and daily management of all nursing activities within Science 37.

Chicago, Illinois, United States

As the director of customer strategy, I collaborate across functional areas of the business to create, develop and implement strategies to enhance customer acquisition, service and satisfaction.

Chicago, Illinois

Firma is a boutique contract research organization that believes a patient-centric approach is the key to unlocking positive outcomes in the drug and medical device development process. Using an integrated suite of specialized solutions, Firma makes the clinical trials process easier and more valuable for patients, and produces higher-quality data for sites and sponsors.In my role, I’m responsible for oversight and management of clinical research studies and projects. Establishes corporate objectives with VP. Identifies new opportunities with Business Development team. Develops and completes RFIs and RFPs as well as attends and presents as Client meetings. Complies with quality management system and good clinical practices through training, processes and early issue identification and training. Develops and tracks KPIs relating to clinical research studies. Contributes to management review meetings as well as overseeing clinical operations metrics. Oversees departmental activities and personnel allocating internal and external resources across projects. Provides guidance, mentorship, training and supervision to departmental personnel.

Greater Chicago Area

Firma is a boutique contract research organization that believes a patient-centric approach is the key to unlocking positive outcomes in the drug and medical device development process. Using an integrated suite of specialized solutions, Firma makes the clinical trials process easier and more valuable for patients, and produces higher-quality data for sites and sponsors. In my role, I'm responsible for oversight and management of in-home study visits.

Greater Chicago Area

West Bend Wi

Record and assess volunteer adverse events with further escalation to medical personnel for evaluation & treatment as warranted.Contributes and is accountable for a secure and appropriate storage of all drug supplies. Ensures effective verbal and written communications inter and intra departmentally in the planning and implementation of volunteer clinical research regimens.Develops and implements innovative nursing research interventions that reflect an ability to make discriminating assessments for complex research projects.Participates in quality assurance of clinical research projects and initiates the need for same as it impacts on clinical practice.Readily accepts responsibility and is accountable for own and delegated activities.

West Bend, Wi

Responsible for study unit activities related to the conduct of clinical trials with emphasis on the safety and welfare of study participants. This may involve some project related responsibilities by coordinating activities for routine studies in compliance with protocol, Standard Operating Procedures (SOPs) and regulatory guidelines from the inception of the protocol throughout the completion of the database lock process.

West Bend, Wi

Under supervision of a Clinical Research Coordinator: Performs set-up, execution, and closeout for study activities related to the conduct of clinical trials with emphasis on the safety and welfare of study participants. Perform project/study management related responsibilities by coordinating activities for Clinical Pharmacology Studies in compliance with protocol, Standard Operating Procedures (SOPs) and regulatory guidelines from the inception of the protocol throughout completion of the database lock process. This involves working closely with all functional areas as well as external providers to ensure consistent high quality study outcomes.

West Bend, Wi

St. Joes

Medical-Surgical

Nuclear Medicine Technologist (CNMT)

Master Of Business Administration (M.B.A.), Dual Degree Msn/Mba

Bachelor'S Degree, Nursing Science, Deans List & High Honors

Associate'S Degree, Registered Nursing/Registered Nurse

Associates, Nuclear Medicine

Associates, Surgical Technology