Jessica Osunde
Dallas,TX
Summary
Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities. Knowledgeable CRC adept at recognizing clinical values and abstract data from source documents. Uses analytical skills to identify data or patient safety issues.
Overview
12
12
years of professional experience
1
1
Certification
Work History
Clinical Research Coordinator
Ut Southwestern Medical Center
04.2023 - Current
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Collected data and followed research protocols, operations manuals, and case report form requirements.
- Followed informed consent processes and maintained records.
- Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Gathered, processed, and shipped lab specimens.
Clinical Research Coordinator
Zenos Clinical Research, Medical City
05.2022 - 02.2023
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Collected data and followed research protocols for seven major trials on. site, operations manuals
- Followed informed consent processes and maintained records for over 100 subjects.
- Collected, evaluated, and modeled collected data.
- Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Gathered, processed, and shipped lab specimens following IATA guidelines.
- Maintained compliance with protocols covering patient care and clinical trial operations
Epidemiologist(Public Health Consultant)
Department Of Health And Human Services
02.2021 - 04.2022
- Collaborated with local organizations to expand health services and resources.
- Participated in health promotion campaigns to raise awareness of health issues.
- Engaged clients in health-related activities to enhance overall well-being.
- Contacted clients in person, by phone or in writing to ascertain compliance with required or recommended actions.
- Provided crisis intervention and supportive counseling services to assist clients facing issues and problems.
- Targeted specific community groups with wellness and disease management information.
- Developed and implemented training classes to educate team members and community residents.
- Wrote and distributed informational materials on chronic diseases, infant mortality, substance abuse, and other community health concerns.
Clinical Research Specialist
Pfizer Pharmaceuticals
01.2017 - 01.2020
- Assisted with analysis of research data in collaboration with research department.
- Prepared scholarly manuscripts and final study reports to communicate results of research to broader scientific community.
- Supervised data collection by core research staff.
- Attended and gave seminars under direction of scientific director.
- Performed data analysis and interpretation of results from clinical trials and epidemiological studies.
Clinical Research Consultant
Medicine And Healthcare Regulatory Agency
01.2012 - 12.2016
- Conducted literature reviews and synthesized research findings.
- Optimized performance, quality, coverage and health outcomes.
- Improved policy and expanded knowledge of health care and human service systems.
- Created strategies for institutions, communities, associations, foundations, governments and people to improve health care and human services systems.
- Designed, constructed and implemented research proposals, protocols and procedures.
- Attended and gave seminars under direction of scientific director.
- Prepared scholarly manuscripts and final study reports to communicate results of research to broader scientific community.
- Assisted with analysis of research data in collaboration with research department.
Education
Master of Science - MPH
University of Aberdeen
UKBachelor of Science - Pharmacy
University of Benin
Benin CityICH-GCP
Clinical Research Fast Track Academy
Arizona07.2023
Skills
- Informed Consenting & Good Clinical Practice
- Case Report Management & Data Analysis
- Study Coordination & Monitoring
- Research Sops Understanding
- Investigator Coordination $ Creative Thinking
- Study Protocols & Adverse Event Documentation
- Planning and Coordination
Certification
ICH-GCP
IATA
CPR
Timeline
Clinical Research Coordinator
Ut Southwestern Medical Center
04.2023 - Current
Clinical Research Coordinator
Zenos Clinical Research, Medical City
05.2022 - 02.2023
Epidemiologist(Public Health Consultant)
Department Of Health And Human Services
02.2021 - 04.2022
Clinical Research Specialist
Pfizer Pharmaceuticals
01.2017 - 01.2020
Clinical Research Consultant
Medicine And Healthcare Regulatory Agency
01.2012 - 12.2016
Master of Science - MPH
University of Aberdeen
Bachelor of Science - Pharmacy
University of Benin
ICH-GCP
Clinical Research Fast Track Academy
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