Kristen Sherrill

• Oversaw daily operations and ensured compliance with regulatory standards.
• Managed team performance through effective training and mentoring programs.
• Developed and implemented strategic initiatives to enhance patient engagement.
• Analyzed operational data to identify areas for process improvement and innovation.
• Ensured compliance with safety regulations and standards in the workplace.
• Maintained productive communication between relevant parties.
• Oversaw inventory management activities such as tracking stock levels and ordering supplies.
• Conducted regular meetings with staff to review performance metrics and identify areas for improvement.
• Scheduled maintenance services to keep equipment functioning properly at all times.
• Collaborated with team members to develop innovative solutions for operational challenges.
• Monitored daily activities of site personnel to ensure quality assurance standards were met.
• Managed relationships with vendors, contractors, and other external stakeholders.
• Reviewed employee performance evaluations regularly to ensure equitable treatment among staff members.
• Supervised projects to uphold schedule requirements and quality demands.
• Established and maintained close working relationships with staff, clients and vendors.
• Facilitated staff meetings to convey policy changes and hear employee input.

• Collected vital signs and laboratory specimens to facilitate testing.
• Observed patients after administration of designated medication for adverse events.
• Screened research study candidates for eligibility and obtained consent documentation.
• Documented case report forms and collected data for study research logs.
• Relayed information such as requirements and instructions from clinical team to study participants.
• Recruited, interviewed and enrolled patients to increase number of participants.
• Prepared for upcoming studies by collaborating with program leaders to determine facility and staff needs.
• Obtained informed consent from research subjects and guardians to explain possible side-effects and potential outcomes of research.
• Helped patients and families feel comfortable during challenging and stressful situations, promoting recovery and reducing compliance issues.
• Assessed patient conditions, monitored behaviors and updated supervising physicians with observations and concerns.
• Maintained strict patient data procedures to comply with HIPAA laws and prevent information breaches.
• Advocated for patient needs with interdisciplinary team and implemented outlined treatment plans.
• Observed strict safety measures, including checking medication dosages before administration to patients.
• Administered oral, IV and intra-muscular medications and monitored patient reactions.

• Spearheaded entire onboarding and orientation process for new employees, providing education and information to facilitate learning and improve employee job satisfaction.
• Participated in brainstorming sessions and team meetings to identify deficiencies and recommend changes to policies and procedures.
• Developed effective approaches to tap employees' potential and build competencies to achieve employer’s goals.
• Mentored team members to succeed and advance within department and company.
• Planned and led training programs on staff development to enhance employee knowledge, engagement, satisfaction and performance.
• Analyzed employees' skill levels and implemented new techniques to boost staff knowledge.

-Responible for the coordination of various clinical trials

-Perform Visit procedures including venipuncture, vitals, injections, EKGs, bladder scans

-assist physician with other necessary procedures, report health and safety information for clinical trial participants.

-Responsible for start up packages for new trials

-Point of contact for sponsors and PIs

-Obtain signatures for all required documentation for trials

-Responsible for maintaining office supplies

• Collaborated with sponsors and investigators to carry out efficient and fully compliant research trials.
• Conducted informed consent presentations and maintained documentation.
• Reviewed site regulatory binder to check collection procedures and completeness of paperwork.
• Adhered to standards in all areas, including data collection, research protocols and regulatory reporting.
• Obtained informed consent of research subjects or guardians
• Evaluated proof of eligibility and consent for participants.
• Participated in regulatory activities and submission by adhering to independent ethics committee and regulatory board.

-Responsible for medications for a unit of patients

-Provided wound treatment for patients

-Perform various charting and documenting of various patient care

-Responsible for supervision of shift CNAs

-Clinical Rotation in telemetry, OB/GYN, medical/surgical, pediatric, geriatric.

-Performed data collection, utilized time management skills and organized priority of care

-Medicaiton administration, measured vital signs , utilized computer charting

-Provided patient education

-Performed wound care

-Peformed venipuncture and collected other carious lab samples

-Issued both personal and mortgage loans as a licensed mortgage officer

-Responsible for collection of past due accounts

-Accounts receivable for payments of customer loans

-Provided excellent customer service to clients