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Cecilia Bosco

@ceciliabosco

Message

I lead compliant, end-to-end clinical trials across oncology and rare diseases.

Brazil

Message

What I'm looking for

I'm looking to lead end-to-end clinical studies where I can strengthen quality, inspection readiness, timelines, budgets, and cross-functional delivery across international oncology or rare disease programs.

I manage clinical research projects end-to-end at AZIDUS, leading study startup through closeout across scope, timelines, quality, budgets, vendors, sites, and Trial Master File readiness.

Previously at IQVIA and Labcorp, I coordinated multidisciplinary teams, study startup, monitoring processes, regulatory and ethics submissions, risk mitigation, financial forecasting, and inspection-ready delivery under ICH/GCP and applicable regulations. My clinical trial experience spans Phase 1–3 studies in oncology, renal disease, leukemia, glioblastoma, and multiple myeloma.

I also bring an MD, MSc, and PhD in Cancer Studies, along with published epidemiological and oncology research. I work fluently in English, Spanish, and Portuguese and have supported international, multi-country studies.

Experience

Work history, roles, and key accomplishments

Current

Clinical Trial and Project Manager

Current

AZIDUS

Oct 2025 - Present (11 months)

Manages clinical research projects end-to-end, ensuring delivery on scope, timelines, quality, and budget. Oversees site management, vendor relationships, TMF inspection readiness, and financial forecasting.

Clinical Project Management Site management Vendor Management TMF Budget Management Risk Mitigation Stakeholder Management ICH GCP KPI Tracking

Associate Project Manager

IQVIA

Jul 2024 - Aug 2025 (1 year 1 month)

Managed clinical operational and quality aspects of studies in compliance with ICH/GCP, serving as primary operational point of contact for sponsors and sites. Coordinated study start-up, TMF maintenance, and risk mitigation strategies.

Clinical Operations ICH GCP TMF Study Start Up Risk Management Vendor Management Financial Reporting

Project Coordinator

IQVIA

Nov 2022 - Jul 2024 (1 year 8 months)

Tracked project metrics, maintained timelines, and supported TMF documentation. Managed purchase orders, protocol deviation tracking, and vendor oversight for translations.

Project Coordination TMF Metrics Vendor Management Protocol Deviations Purchase Order Management Meeting Coordination Documentation

In-House Clinical Research Associate

Labcorp

Aug 2021 - Oct 2022 (1 year 2 months)

Served as contact for project teams and investigative sites, conducting site contacts and monitoring performance. Coordinated study visits, drug shipments, and regulatory submissions.

Clinical Monitoring Site management Regulatory Submissions ICH GCP Data Integrity

Safety Associate

Labcorp

Jan 2021 - Aug 2021 (7 months)

Processed adverse event reports per Safety Management Plan, produced safety data queries, and maintained PSS metrics. Translated source adverse event reports from Spanish and Portuguese into English.

Pharmacovigilance Adverse Event Reporting safety management Data Reconciliation Translation

Visiting Research Associate

King's College London

Apr 2018 - Dec 2020 (2 years 8 months)

Designed and conducted epidemiological observational studies using Swedish databases to evaluate prostate cancer outcomes. Provided statistical and epidemiological guidance for clinical projects and supervised medical students.

Epidemiology Biostatistics Meta Analysis Medical Writing Observational Studies Supervision