Clinical Research Coordinator with Recruitment & Operations Expertise

Certifications

●Google Project Management Certification

●Clinical Research Professional Preparation and GCP Review Course Certificate

●Phlebotomy and EKG Certificate of Completion and Licensure

●ACRP Clinical Research CCRC prep course Certifications.

●CCRC Certification exam qualified

●Bachelors in Pharmacology

Work Experience

Care access : Travel Clinical Site manager/Clinical Research Coordinator

tristate area, NY

August 2024 - July 2025

●Made innovations the development of recruitment plan and obtains listing of potential candidates to contact from project database leading to a 25% increase in participants at site.

●Actively works with the recruitment team in calling and recruiting subjects increasing participant retention rate 15%.

●Held meetings to assist with the creation of appropriate recruitment materials.

●Attends Investigator meetings as required.

●Assist in the creation and review of source documents and road maps milestones during the health screening.

●Responsible for inventory management for on site protocol initiation (lab kits, study medication, specialized equipment, centrifuge)

●Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical guidelines. Liaisons with stakeholders invested in the screening.

●Manage and maintain effective relationships with study participants and colleagues, calling team meetings creating a sensible work environment increasing efficiency.

●Interact in a positive, professional manner with patients, sponsor representatives, investigators and research personnel and management.

●Review project guidelines, making sustainable changes on roadmaps and projects.

●Identified adverse events (AEs) and Serious Adverse Events (SAEs) and notify Investigator where appropriate.

Northwell Health: Clinical Research Coordinator:

manhasset, NY September 2023- May 2024

●Responsible for coordination of 20+ oncology studies involving labs such as Cold Spring Harbor and Wigler Labs. In research projects oversees implementation of study procedures, and the collection and processing of data.

●Performing phlebotomy, electrocardiograms, or monitor vital signs on study participants. Reports findings to the supervisor.

●Collects, labels, logs, processes, and ships biological specimens for analysis according to protocol to ensure proper transportation according to GCP and study SOP’s.

●Collecting data, confers with PI and forwards results to sponsor (internal or external).

●Adheres to Good Clinical Practice and complies with regulatory and grant agency requirements. Follow protocol as developed. Keeps investigators or supervisors informed of developments.

●Ensures availability of equipment for studies. Maintaining specimen and equipment accountability logs.

●Liaisons with agencies including: IRB, OCG, pharmaceutical companies, laboratories, and equipment and supply companies, as needed.

Clinical Directors Network: Clinical Research Coordinator/Clinical Project Manager

Midtown, NY September 2022- November 2023

●Working as a CRC in charge of participants of a multi-centered study at two sites.

●Promoted to manager of multi-centered study (WET) and a Columbia correlated study involving apps and wearable devices for diabetes management.

●Administering study questionnaires to participants.

●Contacting and scheduling participants for follow-up visits at SOP scheduled intervals, streamlining the process increasing callbacks and follow ups by 40%.

●Performing and organizing data entry with Redcap for study to ensure data fidelity.

●Managing on-site visits, obtaining study data and biospecimens.

●Presenting at weekly meetings with primary investigators presenting study progress and the plans moving forward.

●Improved data handling and safety with a new application of Excel and improvement on Redcap.

Weill Cornell Medical Center: Patient Research Coordinator

Upper East Side, NY January 2022 – May 2022

●Worked on NIH-funded study “All Of Us Research Program” and have CITI certifications such as Good Clinical Practices (GCP) Certification.

●Independent study coordination including screening of prospective patients for protocol eligibility and participating in the informed consent process.

●Identified quality and performance improvement opportunities and collaborated with staff in the development of action plans to improve quality.

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