Denishia Dyle
Birmingham,AL
Summary
Results-driven research professional prepared for challenges of overseeing clinical studies. Proven track record of managing complex projects and ensuring compliance with research protocols. Known for fostering team collaboration and adapting to evolving project needs, while excelling in data management and regulatory adherence.
Overview
1
1
year of professional experience
Work History
Clinical Research Coordinator
UAB Medicine
03.2025 - Current
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Gathered, processed, and shipped lab specimens.
- Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
- Followed informed consent processes and maintained records.
- Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
- Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Managed patient recruitment, informed consent process and data entry to support trial objectives.
- Increased participant retention rates through proactive follow-up efforts and regular engagement activities.
- Collected data and followed research protocols, operations manuals, and case report form requirements.
- Reduced data entry errors by implementing stringent quality control measures throughout the study lifecycle.
- Developed strong relationships with trial sponsors, ensuring ongoing collaboration and future project opportunities.
- Monitored patient safety throughout clinical trials and reported any adverse events.
- Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
- Coordinated with cross-functional teams to ensure timely completion of clinical trial milestones.
- Maintained compliance with regulatory guidelines through rigorous documentation and protocol adherence.
- Streamlined data collection processes for increased efficiency and accuracy in study results.
- Coordinated with multiple departments to ensure compliance with regulatory standards, leading to successful trial audits.
- Streamlined patient visit schedules, reducing wait times and increasing patient satisfaction.
- Monitored adverse events and ensured timely reporting to regulatory bodies, maintaining high safety standards.
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
Palliative Care Coordinator
Contessa Health
10.2024 - 03.2025
- Facilitated end-of-life discussions with patients and families, ensuring their wishes were respected in the development of individualized care plans.
- Assessed patient symptoms regularly to inform intervention adjustments as needed while maintaining open lines of communication with the multidisciplinary team.
- Increased access to palliative care services by identifying eligible patients and providing prompt referrals for appropriate care interventions.
- Navigated complex insurance systems effectively to secure coverage for essential palliative services when needed.
- Improved patient comfort by addressing individual needs, coordinating with care teams, and developing personalized care plans.
- Ordered all pharmacy supplies and kept check on inventory levels.
- Discussed medical histories with patients in effort to provide most effective medical advice.
- Scheduled surgeries, managed pre-certifications and verified insurance coverage.
- Coordinated bereavement support services for families following the loss of a loved one, connecting them with appropriate resources as needed.
- Developed strong relationships with community partners for seamless referral processes and enhanced continuity of care across settings.
Patient Recruiter/ Research Assistant
Alcanza
01.2024 - 07.2024
- Increased patient recruitment by developing targeted marketing materials and strategies.
- Completed necessary reports and documentation on time and to specifications.
- Monitored patient progress and reported changes to healthcare professionals.
- Took and recorded patients' vital signs, documenting in medical charts.
- Answered patient inquiries and provided information about healthcare services.
- Cleaned and set up rooms in preparation for patient appointments.
- Scheduled patients for appointments and maintained master calendar.
- Provided family members with general health education and tips for patient care.
- Performed basic laboratory tests and collected specimens for further testing.
- Obtained patient or family member authorizations for tests and procedures.
- Administered medications and injections as directed by healthcare professionals.
- Analyzed complex data sets to uncover critical insights, driving direction of research projects.
- Translated research findings into actionable recommendations, influencing policy and practice.
- Streamlined project workflow, optimizing team efficiency through development of detailed scheduling and tracking systems.
- Recorded and analyzed data to produce reports of results.
- Participated in research projects by designing and executing experiments.
- Participated in lab meetings and project presentations.
- Analyzed results using analytical software and created reports.
- Conducted thorough pre-screening interviews to identify eligible candidates for specific clinical trials or studies.
- Streamlined communication channels between patients, healthcare providers, and research teams for improved coordination.
Education
High School Diploma -
Tarrant High School
Tarrant 05.1995
Bachelor of Arts - HealthCare Administration
Troy University
Troy, AL05.2028
Skills
- Good clinical practices
- Electronic data capture
- Documentation management
- Data analysis
- Informed consent process
- Patient recruitment
- Research experience
- Participant screening
- Records maintenance
- Clinical research ethics
- Meeting coordination
- Report preparation
- Good clinical practice
- Investigator coordination
- Time management
- Problem-solving
- Teamwork and collaboration
- Conflict resolution
- Organizational skills
- Protocol review
- Records management
- Decision-making
Timeline
Clinical Research Coordinator
UAB Medicine
03.2025 - Current
Palliative Care Coordinator
Contessa Health
10.2024 - 03.2025
Patient Recruiter/ Research Assistant
Alcanza
01.2024 - 07.2024
High School Diploma -
Tarrant High School
Bachelor of Arts - HealthCare Administration
Troy University
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