As a member of Beaufort's global project team, I perform a wide variety of clinical trial site activities that maximize performance while ensuring site compliance with protocols, SOPs, and regulatory guidelines. I work directly with investigators and site staff, along with clients, and generate reports as needed for internal stakeholders and clients.• Plan, implement, and oversee clinical research activities in accordance with timelines, budgets, and project deliverables under the… Show more As a member of Beaufort's global project team, I perform a wide variety of clinical trial site activities that maximize performance while ensuring site compliance with protocols, SOPs, and regulatory guidelines. I work directly with investigators and site staff, along with clients, and generate reports as needed for internal stakeholders and clients.• Plan, implement, and oversee clinical research activities in accordance with timelines, budgets, and project deliverables under the guidance of Clinical Project Manager.• Develop or assist in creation, completion, and electronic filing of key study documents (e.g., Study Protocol, Monitoring Plan, Site Training Manual, CRFs, Statistical Analysis Plan, and Data Management Plan).• Prepare activity reports for internal and external distribution and lead sponsor meetings.• Assist in oversight and collection of all project related data and information across multiple studies and ensure data quality and compliance with protocol, SOPs, and regulations at assigned study sites.• Support Project Managers in identifying, addressing, and resolving study issues in alignment with protocols and SOPs.• Collaborate with other members of the Clinical Research team to conduct phone screens with potential clinical sites and maintain communications with CRAs and sites throughout trial process to ensure efficient study logistics.• Identify investigative sites and complete Site Qualification Visits to assure adequate qualifications, training, and resources.• Complete remote monitoring, initiate data query resolution, and track queries to confirm resolution in a timely manner.• Manage clinical document processing and filing associated and conduct clinical administration internal reviews of documents.• Maintain both electronic and physical Trial Master Files.• Create electronic trackers to follow and record study data.• Collect and maintain study metrics (clinical metrics, financial, timeline). Show less

Reviewed and prepared binders and manuals to send to clinical sites. Reviewed regulatory documents to ensure that fulfill ALCOA requirements for regulatory submission.• Responsible for the clinical document processing and filing associated with a clinical study, as well as preparing/maintaining project files (both electronic and hard-copy), documentation binders, clinical forms and logs, and other administrative tasks.• Regularly collect project-related data and information and… Show more Reviewed and prepared binders and manuals to send to clinical sites. Reviewed regulatory documents to ensure that fulfill ALCOA requirements for regulatory submission.• Responsible for the clinical document processing and filing associated with a clinical study, as well as preparing/maintaining project files (both electronic and hard-copy), documentation binders, clinical forms and logs, and other administrative tasks.• Regularly collect project-related data and information and prepares activity reports for internal and external distribution.• Work with other members of a project team to conduct phone screens with hospitals, doctor's offices and other clinical sites that are interested in participating in the studies that Beaufort manages. Show less

As the project manager and executive assistant for Leadout Systems, I was in charge of coordination, day to day activities and general tasking for this family owned IT company. • Managed the coordination of technical projects for an IT company in four states to include an international non-profit which resulted in execution of over 19 projects totaling $182,000 in sales for FY 2022.• Direct liaison between key executive staff which managed schedules, prioritized projects and… Show more As the project manager and executive assistant for Leadout Systems, I was in charge of coordination, day to day activities and general tasking for this family owned IT company. • Managed the coordination of technical projects for an IT company in four states to include an international non-profit which resulted in execution of over 19 projects totaling $182,000 in sales for FY 2022.• Direct liaison between key executive staff which managed schedules, prioritized projects and reviewed staff needs to ensure smooth operation of company day to day functions.• Managed company’s CRM suite, entering leads and associated data from sales executives creating a dedicated pathway for lead cultivation which led to a 74.5% conversion rate.Leadout System's primary service area revolves around managed services related to SMB business IT consulting, engineering, break-fix helpdesk, network architecture design and customer service experiences. Creation of unique portable commercial networks & seat deployment for austere work environments is a hallmark of our company serving several statewide DOT & heavy industrial clients. Show less

Received and inspected unprocessed tissue for discrepancies; stored tissue in designated areas. Processed Dermis tissue through adipose removal, cutting grafts and final packaging. Lead technician responsible for the preparation of aliquots. Cross-trained in processing, packaging and shipping Chondrofix tissue.

Collected samples of plasma to be tested, put bottles in freezer, properly stored samples, entered donor information into the system and helped prepare samples for shipping. Trained to screen donors, including taking basic vitals, in order to determine their eligibility to donate, enter the information into the donor management system and assist them with any questions.