Rescha Mullings
Knoxville
Summary
Clinical research coordinator with extensive experience in adhering to study protocols and good clinical practices. Proven problem-solver with exceptional attention to detail. Ready to leverage years of expertise in a dynamic, fast-paced environment.
Overview
15
15
years of professional experience
Work History
Medical Chaparone
Winbigler Medical
Maryville
05.2022 - 04.2025
- Assisted healthcare providers with patient examinations and procedures.
- Managed patient records using electronic health record systems.
- Prepared examination rooms, ensuring cleanliness and readiness for patients.
- Scheduled patient appointments and coordinated follow-up visits effectively.
- Collected patient information, including medical history, and vital signs, accurately.
- Educated patients on treatments, medications, and preventive care practices.
- Assisted physicians with patient care by taking vital signs, patient histories and preparing patients for examinations.
- Administered injections, medications and treatments as directed by the physician.
- Adhered to HIPAA regulations regarding safeguarding confidential patient information at all times.
- Documented notes during patient visits.
- Relayed messages from patients to physicians about concerns, condition updates or refill requests to facilitate treatment.
Clinical Research Coordinator
AMR
Knoxville
12.2015 - 02.2022
- Coordinated clinical trial activities to ensure compliance with protocols and regulations.
- Managed participant recruitment and screening processes for various studies.
- Organized and maintained study documentation, including consent forms and regulatory files.
- Collaborated with investigators to facilitate effective communication during trials.
- Trained and supervised research staff on protocol adherence and best practices.
- Scheduled and conducted monitoring visits with sponsors to review study progress.
- Oversaw data collection processes to ensure accuracy and reliability of research findings.
- Assisted in the development of study materials, including case report forms and questionnaires.
- Communicated effectively with investigators, study staff, sponsors, vendors, IRB personnel, and other stakeholders throughout the life cycle of the trial.
- Maintained accurate up-to-date tracking logs for all aspects of clinical research activities including but not limited to adverse events, serious adverse events, concomitant medications, lab results .
- Monitored patient safety during clinical trials according to established guidelines.
- Collaborated with sponsors and investigators to carry out efficient and fully compliant research trials.
- Reviewed CRFs for completeness and accuracy before database entry.
- Adhered to standards in areas involving data collection, research protocols, and regulatory reporting.
- Kept patient care protocols and clinical trial operations in compliance.
- Conducted routine visits to research sites to ensure compliance with protocol requirements.
- Reviewed medical records for accuracy of source documentation prior to database lock.
- Collected, processed and delivered specimens from trial participants.
- Developed and maintained accurate and timely study databases.
- Compiled trial related documents into a master file as required by sponsor or regulatory agency.
CNA
St. Mary's General Hospital
Knoxville
07.2010 - 01.2017
- Assisted patients with daily living activities and personal hygiene.
- Monitored vital signs and reported changes to nursing staff.
- Maintained a clean and safe environment for patients and staff.
- Documented patient care activities in electronic health records accurately.
- Trained new nursing assistants on hospital policies and procedures.
- Provided assistance with activities of daily living, including bathing, dressing and grooming.
- Documented patient care services by charting in designated areas.
Education
Associate of Science - Nursing
Pellissippi State Community College
Knoxville, TN12-2010
Skills
- Electronic health records
- Patient record management
- Regulatory compliance
- Clinical trial coordination
- Specimen processing
- Patient care coordination
Affiliations
- Coordinated a Covid vaccine study with Pfizer
- Collaborated and Coordinated a study for esketamine, inhalation medication for depression
Timeline
Medical Chaparone
Winbigler Medical
05.2022 - 04.2025
Clinical Research Coordinator
AMR
12.2015 - 02.2022
CNA
St. Mary's General Hospital
07.2010 - 01.2017
Associate of Science - Nursing
Pellissippi State Community College
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