Highly qualified and results driven health care professional with proven track record and success in building strong relationships with patients and clients. Energetic and goal-oriented with an impressive performance record and well-rounded background in optimizing internal performance. Currently seeking a position which will utilize all skills, abilities, and areas of expertise.
Overview
21
21
years of professional experience
Work History
Senior Clinical Research Associate
Thermo Fisher
12.2023 - Current
Conduct initiation, monitoring and closeout visits to verify study procedures, regulatory documents and data completion.
Improve clinical trial efficiency by streamlining data collection and management processes.
Enhance patient safety through meticulous monitoring of adverse events and protocol compliance.
Reduce study timelines by effectively managing multiple concurrent clinical trials across various therapeutic areas.
Strengthen collaboration with cross-functional teams, ensuring clear communication and alignment on project goals.
Perform study drug accountability and reconciliation via Interactive Response Technology and site drug repository.
Follow drug storage procedures to comply with protocols and SOP requirements.
Senior Clinical Research Associate
Worldwide Clinical Trials
08.2021 - 12.2023
Conducted initiation, monitoring and closeout visits to verify study procedures, regulatory documents and data completion.
Improved clinical trial efficiency by streamlining data collection and management processes allowing 100% data cut deadline milestone 2 cycles in a row.
Enhanced patient safety through meticulous monitoring of adverse events and protocol compliance decreasing protocol deviations by 40%.
Reduced study timelines by effectively managing multiple concurrent clinical trials across various therapeutic areas.
Strengthened collaboration with cross-functional teams, ensuring clear communication and alignment on project goals.
Performed study drug accountability and reconciliation via Interactive Response Technology and site drug repository.
Followed drug storage procedures to comply with protocols and SOP requirements.
Developed strong relationships with investigators and site staff, fostering a culture of trust and open communication throughout the study duration.
Streamlined vendor management processes for more efficient service delivery in support of clinical trial activities.
Provided expert guidance to junior team members, fostering a culture of continuous learning and professional growth.
Senior Clinical Research Associate I
IQVIA
09.2019 - 08.2021
Conducted initiation, monitoring and closeout visits to verify study procedures, regulatory documents and data completion.
Improved clinical trial efficiency by streamlining data collection and management processes.
Enhanced patient safety through meticulous monitoring of adverse events and protocol compliance.
Reduced study timelines by effectively managing multiple concurrent clinical trials across various therapeutic areas.
Strengthened collaboration with cross-functional teams, ensuring clear communication and alignment on project goals.
Played an instrumental role in driving enrollment success by collaborating closely with sites on recruitment strategies tailored to specific patient populations allowing recruitment goal to be met 3 months ahead of schedule.
Implemented electronic data capturing systems to adhere with clinical research guidelines.
Directed, guided and delegated tasks to teams and developed project schedules, resource requirements and timelines to maintain productivity on goals and objectives.
Performed study drug accountability and reconciliation via Interactive Response Technology and site drug repository.
Followed drug storage procedures to comply with protocols and SOP requirements.
Clinical Research Associate II
PPD
04.2017 - 06.2019
Conducted initiation, monitoring and closeout visits to verify study procedures, regulatory documents and data completion.
Improved patient enrollment by developing and implementing effective recruitment strategies.
Enhanced data quality by closely monitoring study progress and ensuring accurate data collection.