Israel Eyi
Liberty Towship,OHIO
Summary
Detail-oriented Clinical Research Associate well-versed in coordinating operations, managing sites and drafting detailed clinical reports. Knowledgeable about action planning, database locking and standard operating procedures. Supports participant recruitment and management to meet research objectives. Hardworking Senior Clinical Associate successfully leads site evaluations, initiations and closeouts. Well-versed in Oncology, Cardiovascular, Respiratory, Dermatology, Gastrointestinal, and Infectious Diseases trials and of picks up new procedures quickly. Offering advanced planning, problem-solving and communication skills developed over 9+ years of clinical research success.
Overview
12
12
years of professional experience
Work History
Sr. Clinical Research Associate
Advance Clinical Research
09.2022 - Current
- Conducted over 366 initiations, 864 monitoring, and 465 closeout visits to verify study procedures, regulatory documents, and data completion.
- Communicated project status Advance Clinical Research management verbally and through technical documentation and presentations.
- Followed drug storage procedures to comply with protocols and SOP requirements.
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Implemented electronic data-capturing systems to adhere to clinical research guidelines.
- Managed project risk by identifying, quantifying, and monitoring potential threats.
- Reviewed participant eligibility and consent documentation to help researchers achieve accurate and meaningful results.
Sr. Clinical Research Associate II
IQVIA BIOTECH
10.2018 - 07.2022
- Conducted over 360 initiation, 768 monitoring, and 404 closeout visits to verify study procedures, regulatory documents, and data completion.
- Communicated project status IQVIA BIOTECH management verbally and through technical documentation and presentations.
- Implemented electronic data-capturing systems to adhere to clinical research guidelines.
- Managed project risk by identifying, quantifying, and monitoring potential threats.
- Reviewed participant eligibility and consent documentation to help researchers achieve accurate and meaningful results.
- Followed drug storage procedures to comply with protocols and SOP requirements.
- Ensured timely completion of monitoring visits, enabling consistent oversight of site performance and adherence to Good Clinical Practice guidelines.
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
Clinical Research Associate II
Novella Clinical
02.2016 - 10.2018
- Maintained site monitoring schedules to facilitate effective communication with members of clinical team.
- Reviewed clinical data, source documentation, case report forms, and investigative site regulatory files to verify accuracy and completion.
- Conducted over 289 initiation, 537 monitoring, and 332 closeout visits to verify study procedures, regulatory documents, and data completion.
- Implemented electronic data-capturing systems to adhere to clinical research guidelines.
- Submitted routine Novella Clinical reports and follow-up letters to facilitate internal and external communication.
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
Clinical Research Associate
Theorem Clinical Research
01.2014 - 02.2016
- Maintained site monitoring schedules to facilitate effective communication with members of clinical team.
- Reviewed clinical data, source documentation, case report forms, and investigative site regulatory files to verify accuracy and completion.
- Conducted over 18 initiation, 198 monitoring, and 44 closeout visits to verify study procedures, regulatory documents, and data completion.
- Implemented electronic data-capturing systems to adhere to clinical research guidelines.
- Followed drug storage procedures to comply with protocols and SOP requirements.
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
Clinical Research Associate Trainee
Theorem Clinical Research
02.2012 - 01.2014
- Learned how to conduct site initiation, monitoring, and close-out visits with emphasis on areas listed below:
- Coordinating site operations
- Informed Consent Process
- Adverse event reporting
- Clinical trial management
- Therapeutic Area Expertise
- Site Management
- Clinical Study Design
- Report Writing
- Electronic Data Capture Systems
- ICH-GCP guidelines
- Good Clinical Practices
- Study protocols
- Patient recruitment
Education
Bachelor of Science - Technical Management Concentration
DeVry University College
Cincinnati, OH06.2009
Skills
- Informed Consent Process
- Clinical trial management
- Therapeutic Area Expertise
- Site Management
- ICH-GCP guidelines
Timeline
Sr. Clinical Research Associate
Advance Clinical Research
09.2022 - Current
Sr. Clinical Research Associate II
IQVIA BIOTECH
10.2018 - 07.2022
Clinical Research Associate II
Novella Clinical
02.2016 - 10.2018
Clinical Research Associate
Theorem Clinical Research
01.2014 - 02.2016
Clinical Research Associate Trainee
Theorem Clinical Research
02.2012 - 01.2014
Bachelor of Science - Technical Management Concentration
DeVry University College
Similar Profiles
Chinonye OdumoduChinonye Odumodu
Clinical Coordinator at Advance Clinical Research, LLCClinical Coordinator at Advance Clinical Research, LLC
Ramon Hugo SanchezRamon Hugo Sanchez
Principal Investigator at Quantum Research AssociatesPrincipal Investigator at Quantum Research Associates
Zayyad Muhammad KuduZayyad Muhammad Kudu
Senior Strategic Information Officer -CCCRN, State SI Lead at Centre for Clinical Care and Clinical Research NigeriaSenior Strategic Information Officer -CCCRN, State SI Lead at Centre for Clinical Care and Clinical Research Nigeria
ALI SAYYAMALI SAYYAM
Manager of Operations at PHILLY AUTO SALVAGEManager of Operations at PHILLY AUTO SALVAGE
Kei GregoryKei Gregory
Owner at Frost FactoryOwner at Frost Factory