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Francisco Ezequiel Herrera

@franciscoezequielher

Pharmacovigilance Project Coordinator at Insuvia, coordinating international project rollouts and building clinical data analytics skills.

Lithuania

Message

At Insuvia, I coordinate the setup and rollout of international pharmacovigilance projects, including country-level requirements and operational workflows. I also prepare reports and reconciliations, monitor KPIs, and support deviation and CAPA management.

At IQVIA, I conducted clinical trial monitoring, reviewed medical histories and safety information, and supported site teams with protocol compliance and documentation.

At Syneos Health, I supported risk-based monitoring across clinical trial sites, with a focus on oncology studies. I reviewed trial data and monitoring outputs, prepared SCAN reports, and worked with CRAs and site teams.

I’ve also worked in pharmacovigilance at Knight Therapeutics and AbbVie, supporting safety submissions, adverse event case processing, regulatory reporting, and safety data reconciliation. Alongside my clinical research experience, I’ve developed skills in SQL, Python, and Power BI and completed data projects in analytics and data pipelines.

Experience

Work history, roles, and key accomplishments

Current

Pharmacovigilance Project Coordinator

Current

Insuvia

Apr 2024 - Present (2 years 7 months)

Coordinates the setup and rollout of new international pharmacovigilance projects, including country-level requirements and operational workflows. Manages monthly reports, reconciliations, financial reports, and operational documentation, and monitors KPIs and supports deviation and CAPA management.

Pharmacovigilance Project Coordination KPI Monitoring CAPA Deviation Management Documentation English Lithuanian Translation

Clinical Research Associate

IQVIA

Sep 2024 - Dec 2024 (3 months)

Conducted clinical trial monitoring activities, including source data verification/review and investigational product accountability. Reviewed medical histories and clinical safety information, including AEs, SAEs, and AESIs, and supported site teams in maintaining protocol compliance and documentation.

Clinical Trial Monitoring Source Documentation Verification (SDV)Adverse Events SAE AESIs Protocol Compliance Veeva Vault LabCorp

Central Monitor I

Syneos Health

May 2022 - Aug 2024 (2 years 3 months)

Supported risk-based monitoring activities across clinical trial sites, with a focus on oncology studies. Reviewed clinical trial data and monitoring outputs to support data quality and identify potential issues, and prepared SCAN reports while collaborating with CRAs and site teams.

Risk Based Monitoring Central Monitoring Oncology Clinical Data Review SCAN Reports Medidata EDC CTMS Veeva Vault

Pharmacovigilance & Medical Information Regional Senior Analyst

Knight Therapeutics

Nov 2021 - Feb 2022 (3 months)

Supported medical information and pharmacovigilance activities across Latin American markets. Processed safety-related submissions and database entries using ARGUS and SCIMAX, and supported audit activities, corrective and preventive actions, and English-Spanish medical translations.

Pharmacovigilance Medical Information Argus SCIMAX Audit CAPA English Spanish Translation

Pharmacovigilance Analyst

AbbVie

Aug 2019 - Nov 2021 (2 years 3 months)

Processed and assessed adverse event cases, including serious adverse events and SUSARs, in accordance with applicable procedures. Supported regulatory reporting and interactions with Latin American health authorities, including ANMAT, and contributed to periodic safety reporting, metrics, and data reconciliation activities.

Pharmacovigilance Adverse Event Reporting SAE SUSARs Regulatory Reporting ANMAT Data Reconciliation