Dominique Ocampo
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
6
6
years of professional experience
Work History
Clinical Research Associate
PPD
08.2023 - Current
- Achieved a 30% improvement in patient recruitment timelines by developing and executing targeted recruitment strategies
- Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets
- Achieved a 20% reduction in the time taken to report adverse events by implementing streamlined reporting processes
- Maintained a 100% compliance rate with regulatory guidelines and internal SOPs during routine audits
- Traveled to investigative sites to conduct site qualification, initiation, interim monitoring, and close-out visits to maintain and enforce regulatory compliance
- Fostered strong relationships with investigative sites, resulting in a 25% increase in site engagement and cooperation
Associate Clinical Research Manager
PPD
08.2021 - 08.2023
- Conducted and closed out over 43 Phase I-III clinical trials per sponsor and clinical protocols
- Achieved a 100% on-time completion rate for regulatory submissions, ensuring compliance with regulatory requirements
- Effectively communicated and collaborated specific study requirements to the research team, including technicians, paramedics, PK lab, clinical lab, sponsor, monitors, and primary investigators
- Ensured study documents were organized, tracked, maintained, and archived in audit-ready condition
- Orchestrated and executed streamlined patient recruitment strategies, resulting in a 30% reduction in enrollment timelines
- Developed project management tools for tracking progress, facilitating communication among team members, and ensuring timely completion of tasks
Clinical Research Enrollment Coordinator
PPD Early Development
06.2021 - 08.2021
- Demonstrated organizational skills by preparing and organizing 260+ study forms, ensuring precise data capture aligned with sponsor requirements and clinical protocol standards.
- Implemented a systematic filing system that contributed to a 20% reduction in document retrieval time during audits, enhancing overall study documentation efficiency
- Conducted Informed Consent sessions for over 600 prospective subjects, ensuring a comprehensive understanding of study requirements
- Thoroughly reviewed all paperwork and laboratory data to ensure subject eligibility
- Achieved a 15% improvement in data accuracy through meticulous review and enhancement of documentation processes.
Accounting Assistant
Trinity Crating
01.2018 - 01.2020
- Reduced financial discrepancies, effectively reconciling bank accounts and organizing information into accounting software
- Tracked financial progress by creating quarterly and yearly balance sheets
- Managed high-volume invoice processing tasks while consistently meeting tight deadlines for vendor payments
- Expedited invoice processing with effective communication between internal departments and external vendors
Education
Bachelor of Science - Cellular Biology
Texas State University
San Marcos05.2021
Skills
- Informed Consent Process
- Protocol Review
- Quality Assurance
- NDAs
- Pharmacovigilance
- Records Management
- IRB Submissions
- Completing regulatory documents
- ICH Guidelines
- Medication Dispensing
Timeline
Clinical Research Associate
PPD
08.2023 - Current
Associate Clinical Research Manager
PPD
08.2021 - 08.2023
Clinical Research Enrollment Coordinator
PPD Early Development
06.2021 - 08.2021
Accounting Assistant
Trinity Crating
01.2018 - 01.2020
Bachelor of Science - Cellular Biology
Texas State University