Odiesky Compte Rodriguez
Miami,FL
Overview
6
6
years of professional experience
Work History
Clinical Research Coordinator
Exellence Medical & Research
04.2024 - Current
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- 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.
- Facilitated clear communication between principal investigators, sponsors, and study participants for seamless trial execution.
- 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.
- 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.
- 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.
- Contributed to the successful completion of clinical trials by proactively resolving issues, mitigating risks, and meeting deadlines in a fast-paced environment.
- Prepared detailed informed consent documents to clearly communicate risks, benefits, expectations, rights and responsibilities related to participation in clinical trials.
- Maintained compliance with regulatory guidelines through rigorous documentation and protocol adherence.
- Streamlined data collection processes for increased efficiency and accuracy in study results.
- Streamlined patient visit schedules, reducing wait times and increasing patient satisfaction.
- Improved data integrity and accuracy with meticulous oversight of data collection processes.
- Conducted comprehensive reviews of clinical trial protocols to identify and rectify potential issues before study initiation.
- Facilitated communication between research team and study sponsors, ensuring clear and consistent updates on trial progress.
- Collected, evaluated, and modeled collected data.
Medico Ecografista
Ministerio De Salud Publica, Cuba
11.2018 - 10.2022
- Self-motivated, with a strong sense of personal responsibility.
- Worked effectively in fast-paced environments.
- Skilled at working independently and collaboratively in a team environment.
- Proven ability to learn quickly and adapt to new situations.
- Excellent communication skills, both verbal and written.
- Demonstrated respect, friendliness and willingness to help wherever needed.
- Passionate about learning and committed to continual improvement.
- Worked flexible hours across night, weekend, and holiday shifts.
- Developed and maintained courteous and effective working relationships.
Education
Medical Assistant - Medicina
South Florida Institute of Technology
Miami, FL02-2025
Diplomado En Ecografia Diagnostica - Medicina
Universidad De Ciencias Medicas De Villa Clara
Santa Clara, Cuba07-2018
Especialista En Medicina General - Medicina
Universidad De Ciencias Medicas De Villa Clara
Santa Clara, Cuba07-2016
Doctor of Medicine - Medicina
Universidad De Ciencias Medicas De Villa Clara
Santa Clara, Cuba07-2013
Tecnico En Contabilidad Y Finanzas - Contabilidad
Instituto De Economia
Remedios, Villa Clara, Cuba07-2005
High School Diploma -
Escuela Secundaria
Remedios, Villa Clara, Cuba07-2001
No Degree -
Escuela Primaria
Remedios, Villa Clara, Cuba07-1998
Skills
- Informed consent
- Adverse event reporting
- Study protocols
- Patient recruitment
- Data collection techniques
- Participant screening
- Phlebotomy
- Specimen collections
- Specimen handling
- Good clinical practice
Timeline
Clinical Research Coordinator
Exellence Medical & Research
04.2024 - Current
Medico Ecografista
Ministerio De Salud Publica, Cuba
11.2018 - 10.2022
Medical Assistant - Medicina
South Florida Institute of Technology
Diplomado En Ecografia Diagnostica - Medicina
Universidad De Ciencias Medicas De Villa Clara
Especialista En Medicina General - Medicina
Universidad De Ciencias Medicas De Villa Clara
Doctor of Medicine - Medicina
Universidad De Ciencias Medicas De Villa Clara
Tecnico En Contabilidad Y Finanzas - Contabilidad
Instituto De Economia
High School Diploma -
Escuela Secundaria
No Degree -
Escuela Primaria
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