AMANDA ALIU
Terryville
Summary
Clinical Project and Program Leader with extensive experience managing clinical research operations from study start-up through closeout. Proven liaison between sponsors, CROs, and internal teams, driving operational execution, compliance, and performance across complex clinical trials.
Overview
12
12
years of professional experience
Work History
Project Lead, Clinical Research
Care Access
04.2025 - Current
- Liaison between study sponsors, CROs, and internal teams to execute all trial activities from start-up through closeout
- Led and coordinated clinical operations across multiple trials, supporting 100+ employees in achieving project milestones
- Ensure compliance with GCP, FDA regulations, IRB requirements, and sponsor expectations
- Created KPI reports, dashboards, and performance metrics to inform leadership and sponsors on trial progress
- Developed project trackers to implement initiatives and monitor daily activities for streamlined operations
- Partner with leadership to ensure timelines, quality standards, and end goals are met
Central Studies Coordinator, Manager
Care Access
05.2023 - 04.2025
- Managed centralized clinical research operations across multiple studies to ensure compliance and data integrity
- Prepared enrollment, quality, and KPI reports for senior leadership to facilitate informed decision-making
- Mentored and trained clinical research staff, enhancing team knowledge and capabilities
- Coordinated resources, schedules, and cross-functional workflows
Central Studies Coordinator
Care Access
06.2022 - 05.2023
- Oversaw clinical research projects, ensuring alignment with sponsor and CRO timelines
- Developed trackers, spreadsheets, and reporting tools to streamline project management
- Coordinated patient recruitment efforts for clinical trials and research studies.
- Managed scheduling and logistics for study-related meetings and events.
- Collaborated with cross-functional teams to ensure compliance with regulatory standards.
Clinical Research Coordinator
Chase Medical Research
05.2016 - 06.2022
- Coordinated clinical trial activities, including informed consent and data collection, to support trial objectives
- Coordinated clinical trials to ensure compliance with regulatory standards.
- Managed participant recruitment and informed consent processes efficiently.
- Collaborated with investigators to develop study protocols and timelines.
Clinical Research Coordinator
Waterbury Pulmonary Associates
10.2013 - 05.2016
- Coordinated clinical trial activities, facilitating informed consent and ensuring accurate data collection
- Coordinated participant recruitment and enrollment for clinical trials and studies.
- Managed regulatory submissions and ensured compliance with ethical guidelines.
- Scheduled and conducted study visits, collecting necessary data from participants.
Education
Licensed Practical Nurse -
New England Technical Institute
High School Diploma -
Wolcott High School
Skills
- Clinical trial operations
- Project management
- Data collection
- KPI reporting
- Cross-functional collaboration
- Team collaboration
- Staff training
Awards
Silver Award, Care Access, 2024
Timeline
Project Lead, Clinical Research
Care Access
04.2025 - Current
Central Studies Coordinator, Manager
Care Access
05.2023 - 04.2025
Central Studies Coordinator
Care Access
06.2022 - 05.2023
Clinical Research Coordinator
Chase Medical Research
05.2016 - 06.2022
Clinical Research Coordinator
Waterbury Pulmonary Associates
10.2013 - 05.2016
Licensed Practical Nurse -
New England Technical Institute
High School Diploma -
Wolcott High School