Clinical Research Coordinator

Osorochukwu Sonia Obi

**** **** ****, *** ***, Stovkton, CA 95213

(T) 350-***-****

(E) **********@*******.***

Summary of Qualifications

Highly organized and detail-oriented Clinical Research Coordinator with experience managing and coordinating clinical trials. Skilled in study start-up, participant recruitment, and regulatory compliance. Strong interpersonal skills and ability to collaborate effectively with interdisciplinary teams. Dedicated to ensuring the ethical and efficient conduct of clinical research studies. Experience

8/2012 - 3/2025 University Hospital Coventry & Warwickshire, Coventry, Coordinate and manage clinical trials in compliance with applicable regulations and standard operating procedures (SOPs).

Ensure the timely completion of study tasks and met project timelines Screen, recruit, and consent participants for clinical trials and maintain their study records

Conduct and document study visits and procedures, including vital signs, medical history, and medication review

Collaborate with investigators, sponsors, and other team members to ensure the study's success

Participate in the development of study-related documents, such as protocols, informed consent documents, and case report forms (CRFs) Prepare and maintain regulatory documents and submissions, such as IRB applications, progress reports, and safety reports Assist in the collection, analysis, and reporting of study data Train and mentor new clinical research staff members Conducted on-site monitoring visits to ensure protocol and regulatory compliance, data quality, and patient safety

Managed and resolved data queries with study sites Participated in the planning and conduct of investigator meetings Assisted in the development of study documents and materials, such as protocols, informed consent documents, and CRFs

Maintained study files and records in accordance with regulatory requirements and SOPs

Clinical Research Coordinator 11/2023 - 3/2025

Conducted comprehensive reviews of clinical documentation to ensure compliance with regulatory standards.

Collaborated with healthcare providers to improve documentation practices, resulting in a reduction in query response times.

Provided training and support to medical staff on effective documentation techniques, enhancing overall compliance and quality of care. Participated in interdisciplinary team meetings to discuss documentation improvement strategies.

Assisted in the implementation of a new EHR system, enhancing data retrieval and reporting capabilities.

Managed clinical documentation for multiple clinical trials, ensuring accuracy and completeness.

Clinical Documentation Specialist 8/2012 - 10/2023 Collaborated with cross-functional teams to streamline documentation processes, reducing turnaround time.

Facilitated data entry and validation processes for clinical studies, ensuring data integrity.

Assisted in the development of study protocols and documentation templates. Participated in clinical research meetings, providing insights on documentation challenges.

Worked with doctors to improve coding.

Education

Oxford Brookes University, Oxford

2023 M.sc Public Health

Abia State University, Uturu

2010 B.sc Information Science

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