Benjamin O Email & Phone Number

Dynamic Clinical Research Professional with extensive experience in site management, study startup, and audit readiness. Proficient in Good Clinical Practice (GCP) and regulatory compliance, ensuring data integrity through rigorous QC reviews. Strong track record in maintaining IP accountability and driving project management initiatives focused on process improvement. An effective communicator who fosters collaboration among cross-functional teams to achieve successful clinical outcomes. Committed to continuous growth and innovation in the clinical research field.

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  Clinical Trail Project Assitant Ii

  Abbvie

  2021 - Present

  Clinical Project Assistant | Study Start-up | QC Review | Clinical Documentation | Veeva Vault SpecialistExperienced Clinical Project Assistant with a strong background in supporting clinical research initiatives, ensuring regulatory compliance, and streamlining processes. Skilled in site management, study start-up, and document management. Collaborates effectively with cross-functional teams and maintains positive relationships with stakeholders. Possesses exceptional organizational skills, attention to detail, and the ability to prioritize tasks. Utilizes critical thinking and problem-solving abilities to resolve complex issues. Proficient in various software systems. (Veeva Vault, TESLA, Conga CLM, Sharepoint,..)Achievements:- Successfully processed and QC’d thousands of Veeva VaultT Tmf study documents monthly, ensuring data integrity and compliance with regulatory guidelines.-Initiated and managed the prompt processing & distribution of CDAs and CSAs to the sites, ensuring contractual compliance.- Played a key role in coordinating and completing multiple projects within tight timelines, resulting in successful study start-ups and milestones.- Received recognition for maintaining high-quality standards in document management and compliance with industry regulations.- Actively contributed to the improvement of processes and procedures, leading to increased efficiency and productivity.- Demonstrated strong attention to detail and accuracy in conducting meticulous quality control reviews, ensuring the highest level of data accuracy and reliability.- Proactively identified and resolved issues, effectively minimizing risks and ensuring smooth operations throughout the study lifecycle.Passionate about driving operational excellence in clinical research and dedicated to contributing to the advancement of healthcare through quality clinical trial coordination, management, and regulatory compliance.