Angelina Galeano

Regional Study Coordinator Europe

Labcorp

Feb 2024 - Jan 2025 (1 year)

Served as the regional liaison between assigned client representatives, such as Clinical Research Associates (CRAs) or Site Monitors, and LabCorp internal departments and teams. Conducted data locks during mid-study and at the study's conclusion. Monitored, tracked, and resolved all local study issues, particularly logistical challenges and delays in the receipt of study supplies. Provided exceptional customer service and ensured timely responsiveness to enhance client satisfaction.

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Clinical Development Associate

BTGSERB Pharmaceuticals

Jan 2023 - Feb 2024 (1 year 2 months)

Coordinate contracts with CRO Study Managers to ensure timely signatures from sites and the sponsor. Collaborate with study managers at ICON and IQVIA. Register studies on ClinicalTrials.gov and CTIS for EMA studies in France. Follow EMA guidelines and French Authority requirements for clinical trials. Administrative duties include managing meeting minutes, diary management, and tracking study visit payments to CRO's.

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Clinical Trial Coordinator

Liverpool School of Tropical Medicine

Sep 2020 - Sep 2021 (1 year 1 month)

Responsible for starting up 17 recruitment sites across the greater Liverpool area. Ensured procedures complied with regulatory and ethical requirements as well as trial protocols. Submitted applications to local NHS research, HRA, ethics committees (REC), trust research and development (R&D) office, and MHRA for necessary approvals. Assisted in preparing Case Record Forms (CRFs), Standard Operating Procedures (SOPs), and clinical manuals. Responsible for study documentation and TMF management.

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Clinical Administrative Assistant

Liverpool School of Tropical Medicine

Jun 2020 - Sep 2021 (1 year 4 months)

Managed and maintained databases containing essential participant information and visit schedules for all vaccinated individuals. Coordinated over six hundred booster and follow-up appointments for the period of June-August 2020. Collaborated with various teams, including NIHR, Women's, RLH, and Aintree, to establish follow-up sites. Conducted quality control of participant case records in preparation for MHRA inspection, including staff training and GCP compliance. Tracked and updated the database for participant remuneration. Administrative Team Management.

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Project Support Officer – CURE TEAM

Royal Liverpool University Hospital,

Oct 2019 - Jun 2020 (9 months)

Implemented and maintained a database for all service users for CURE TEAM. Updated the Smoke Free Liverpool Database (National Database) on a weekly basis. Consulted with Smoke Free Liverpool for follow-up appointments in the community for service users. Attended Smoke Free Liverpool meetings and community engagement events.

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Clerical Research Assistant/Diabetic Medicine

Royal Liverpool University Hospital

Aug 2009 - Sep 2019 (10 years 2 months)

Responsible for managing databases for all studies in accordance with various study protocols. Input data into Electronic Case Report Forms (CRFs) utilizing systems selected by sponsors, such as RAVE and MEDIDATA. Regularly attended Diabetes Research Network meetings. Collaborated closely with Clinical Research Associates from multiple pharmaceutical companies. Processed amendments from IRAS submitted by sponsors. Localized all approved documents, including Participant Information Sheets (PIS), Informed Consent Forms (ICF), and General Practitioner (GP) letters. Attended Investigator and Close-out Meetings internationally. Coordinated the archiving of all studies.

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