KUNLE OLABODE-GEORGE
Bowie,MD
Summary
Industrious Junior Leader proficiency and willing to learn any job. Highly effective at training and supporting new members with a compassionate and open approach.
Overview
14
14
years of professional experience
Work History
Clinical Research Training
Medstar Southern Maryland Hospital
Clinton, MD
10.2018 - Current
- Conducted quality assurance audits at research sites to ensure adherence to protocols, SOPs, regulations, guidelines.
- Assisted in preparing periodic reports summarizing progress of clinical studies.
- Developed and maintained accurate and timely study databases.
- Performed patient assessments, collected and analyzed data, and prepared reports.
- Reviewed CRFs for completeness and accuracy before database entry.
- Monitored patient safety during clinical trials according to established guidelines.
- Provided guidance on Good Clinical Practice regulations and other applicable regulatory standards.
- Provided training to study staff on protocol requirements and GCP regulations.
- Communicated effectively with investigators, study staff, sponsors, vendors, IRB personnel, and other stakeholders throughout the life cycle of the trial.
- Collaborated with internal departments such as Regulatory Affairs and Data Management to ensure that all studies were conducted in accordance with ICH-GCP guidelines.
- 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 .
- Kept patient care protocols and clinical trial operations in compliance.
- Monitored subject enrollment and tracked dropout details.
Clinical Research Coordinator
Care Access Research, LLC.
Alexandria, VA
03.2023 - 04.2024
- Reviewed medical records for accuracy of source documentation prior to database lock.
- Provided guidance on Good Clinical Practice regulations and other applicable regulatory standards.
- Compiled trial related documents into a master file as required by sponsor or regulatory agency.
- Reviewed CRFs for completeness and accuracy before database entry.
- Communicated effectively with investigators, study staff, sponsors, vendors, IRB personnel, and other stakeholders throughout the life cycle of the trial.
- Provided training to study staff on protocol requirements and GCP regulations.
- Assisted in preparing periodic reports summarizing progress of clinical studies.
- 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 .
- Collaborated with internal departments such as Regulatory Affairs and Data Management to ensure that all studies were conducted in accordance with ICH-GCP guidelines.
- Developed and maintained accurate and timely study databases.
Dialysis Technician
DaVita
SEAT PLEASANT, MD
03.2010 - 08.2019
- Implemented quality improvement initiatives within the facility's dialysis unit.
- Maintained accurate records of patients' medical history and treatment plans in accordance with HIPAA regulations.
- Restocked supplies needed for dialysis procedures in an organized manner.
- Identified and reported any adverse reactions or changes in patient condition to the supervising nurse.
- Collaborated with interdisciplinary team members to ensure best possible outcomes for all patients.
- Performed patient assessments prior to dialysis treatments, including vital signs and weight checks.
- Ensured all safety protocols were followed while performing duties in the dialysis unit.
- Participated in performance improvement activities as required by facility policy.
- Adhered to all applicable laws, regulations, standards, policies and procedures governing healthcare delivery services.
- Evaluated access sites for infection or other complications prior to initiating treatment.
- Calibrated dialysate solution according to prescribed formula for each individual patient's needs.
- Performed daily maintenance on dialysis machines, such as cleaning and sterilization.
- Initiated and terminated reverse osmosis water system and performed water quality monitoring tests prior to dialysis initiation.
- Trained new dialysis technicians on machine operation and patient care procedures.
- Followed infection control measures when cleaning and attaching hemodialysis machine to access sites like fistulas, catheters, and grafts.
- Took and documented patient temperature, blood pressure, pulse and respiration rates before and after dialysis treatment.
Education
Master of Science - Social Work
Grand Canyon University
Phoenix, AZ07-2026
Bachelor of Science - Health Sciences
Grand Canyon University
Phoenix, AZ05-2024
Skills
- Specimen handling
- Medication Dispensing
- Protocol development
- Research experience
- Documentation requirements
- Documentation Management
- Report Preparation
- Database organization
- Scheduling proficiency
Timeline
Clinical Research Coordinator
Care Access Research, LLC.
03.2023 - 04.2024
Clinical Research Training
Medstar Southern Maryland Hospital
10.2018 - Current
Dialysis Technician
DaVita
03.2010 - 08.2019
Master of Science - Social Work
Grand Canyon University
Bachelor of Science - Health Sciences
Grand Canyon University
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