IDA GONZALEZ
NEW PORT RICHEY
Summary
Professional with experience in clinical research coordination, equipped to make significant impact in this field. Demonstrated ability to manage clinical trials, ensure compliance with protocols, and maintain accurate documentation. Strong emphasis on team collaboration, reliability, and adaptability to evolving project requirements. Proficient in patient recruitment, data collection, and regulatory submissions, with results-driven approach that ensures successful study outcomes.
Overview
31
31
years of professional experience
Work History
Clinical Research Coordinator
Suncoast Clinical Research
06.2023 - 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.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Oversaw the management of investigational product supplies, ensuring appropriate storage conditions were maintained at all times for optimal efficacy during trials.
Senior Clinical Research Coordinator
Radiant Research
01.2012 - 06.2023
- Conduct all clinical duties associated with performing clinical trials
- Evaluate patients for eligibility and conduct patient visits per protocol requirements
- Perform venipuncture, clinical lab procedures, ECG’s, Holter monitors, ambulatory blood pressure monitors
- Assure completion of all clinical record keeping in accordance with protocol requirements, medical practice requirements and good clinical practices
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Contributed to the successful completion of clinical trials by proactively resolving issues, mitigating risks, and meeting deadlines in a fast-paced environment.
Clinical Research Coordinator/Dept. Supervisor
Florida Medical Clinic
01.2007 - 01.2011
- Contact CRO and sponsors for new clinical trials
- Conduct all aspects of starting a new research dept
- Contract other facilities for procedures not done in our facility
- Complete all regulatory documents for each trial
- Conduct all site visits and budget requirements for each of the trials
- Conduct all clinical research coordinator duties associated with clinical trials
- Administration of informed consent in compliance with requirements defined in 21 CRF and ICH guidance relating to GCP’s
- Evaluate patients for eligibility and conduct patient visits per protocol requirements
- Perform venipuncture, clinical lab procedures, ECG’s, Holter monitors and other procedures as required by protocol
Clinical Research Coordinator
Arthritis Center Research Dept.
01.2005 - 01.2007
- Administration of informed consent in compliance with requirements defined in 21 CRF and ICH guidance relating to GCP’s
- Conduct all clinical duties associated with performing clinical trials
- Evaluate patients for eligibility and conduct patient visits per protocol requirements
- Perform venipuncture, clinical lab procedures, ECG’s, Holter monitors, ambulatory blood pressure monitors and other procedures as required by protocol
Clinical Research Coordinator
Suncoast Clinical Research
01.1999 - 01.2004
- Conduct all clinical duties associated with performing clinical trials
- Assure completion of all clinical record keeping in accordance with protocol requirements, medical practice requirements and good clinical practices
Clinical Research Coordinator/Medical Assistant
Urology Health Center
01.1994 - 01.1999
- Conduct all clinical duties associated with performing clinical trials
- Assist doctors with patient care including chemo treatments for bladder and prostate cancer
- Ordering medical supplies for clinic area
Education
No Degree - Psychology
Purdue University
Hammond, INSkills
- Good clinical practices
- Electronic data capture
- Documentation management
- Adverse event reporting
Languages
Spanish
Native or Bilingual
Timeline
Clinical Research Coordinator
Suncoast Clinical Research
06.2023 - Current
Senior Clinical Research Coordinator
Radiant Research
01.2012 - 06.2023
Clinical Research Coordinator/Dept. Supervisor
Florida Medical Clinic
01.2007 - 01.2011
Clinical Research Coordinator
Arthritis Center Research Dept.
01.2005 - 01.2007
Clinical Research Coordinator
Suncoast Clinical Research
01.1999 - 01.2004
Clinical Research Coordinator/Medical Assistant
Urology Health Center
01.1994 - 01.1999
No Degree - Psychology
Purdue University
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