Kingsley Nwachie
Plano,TX
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.
Overview
5
5
years of professional experience
Work History
Clinical Research Associate
Bold Consults
06.2022 - Current
- Ensured protocol adherence, conducting regular site visits and providing training to study staff as needed.
- Processed specimens for clinical trials, sample storage and assay to provide registry of samples for test development, validation and analysis.
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Supported the successful completion of clinical trials by proactively managing risks and addressing challenges throughout all stages of the study process.
Clinical Research Associate
Accouns Diagnosis
02.2019 - 06.2022
- Processed specimens for clinical trials, sample storage and assay to provide registry of samples for test development, validation and analysis.
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Supported the successful completion of clinical trials by proactively managing risks and addressing challenges throughout all stages of the study process.
- Conducted clinical trial in accordance with protocol and recorded and monitored progress.
- Collected data and followed research protocols, operations manuals, and case report form requirements.
- Provided clinicians with data to conduct clinical trials and determine methods to prevent, screen for, diagnose and treat disease.
- Reviewed data queries and listings and worked with study centers to resolve data discrepancies.
- Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
- Prepared and maintained regulatory documents for clinical trial submissions.
Education
Bachelor of Arts - Public Administration
Ambrose Alli University
Ekpoma03.2003
Skills
- Drug Accountability
- Clinical Study Reports
- Protocol adherence
- Data Analysis
- Protocol development
- Data Evaluation
- Clinical Documentation
- Report Preparation
Timeline
Clinical Research Associate
Bold Consults
06.2022 - Current
Clinical Research Associate
Accouns Diagnosis
02.2019 - 06.2022
Bachelor of Arts - Public Administration
Ambrose Alli University
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