Cynthia Betros

Senior Clinical Trial Manager @Bristol Myers Squibb

Trenton, NJ, US
MOBILE NUMBERS
+91 *********19

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WORK HISTORY

Dec 2021 — Present

Senior Clinical Trial Manager @Bristol Myers Squibb

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NJ, US

Lead execution and oversight for 8+ clinical trials (Phases 1b/2, 2, 3) across oncology (bladder, breast, colorectal, ovarian, prostate, renal) and Type 1 Diabetes, managing 5–18 sites per study.• Serve as Lead CTM on multiple priority studies (previously led 5), supervising and coordinating cross-functional teams of 5–8 US RCO colleagues, fostered collaboration and accountability through weekly meetings.• Engage in protocol design, ICF development, eCRF development, and clinical study report (CSR) review; participated in adjudication, advisory board, and regulatory submissions. • Mentored +5 junior team members and coached/onboarded 10+ new hires, co-led multiple SME teams, and developed departmental training materials.• Foster collaboration with global stakeholders, both internal (Medical, Regulatory) and external (sites, vendors, labs, IRBs, KOLs) to resolve operational challenges; primary BMS representative for project communications.• Consistently deliver study start-up ahead of target (decreased by 1-6 weeks/~22%); developed a start-up checklist adopted at both country and study levels. Development and delivery of SIV training to 20+ sites. • Identified ~$500K in additional clinical trial funding to enable study continuity.• Directed risk management, CAPA for audits/inspections, and supported regulatory filings and health authority/ethics submissions.• Contributor to RCO Protocol Review Committee (PRC) and cross-functional continuous improvement initiatives for Rave (including UAT and SAE reporting enhancements).• Accountable for end-to-end data review, patient safety, and regulatory compliance; led data cleaning, querying, and safety trend escalation ahead of DBL and Data Monitoring Committees (DMC) milestones.• Led contract negotiations for ITQA agreements between BMS/Celgene and major academic institutions, facilitating multi-study coverage.• Utilizes ChatGTP and BingCoPilot to help improve and streamline performance.

EDUCATION

1996 — 2000

Rutgers University

B.S., Animal Science

2001 — 2006

Rutgers University

MS, Animal Science - Equine Exercise Physiology

SKILLS

Good Laboratory Practice (Glp)GlpClinical DevelopmentStandard Operating Procedure (Sop)Electronic Data ManagementAnalysisU.s. Food and Drug Administration (Fda)Electronic Data Capture (Edc)Clinical TrialsResearchEditingClinical Data ManagementGcpPharmaceutical IndustrySopFdaComputer LiterateBiotechnologyTroubleshootingSoftware DocumentationEdcSocial MediaMicrosoft WordMedical WritingIch-GcpClinical MonitoringProject ManagementIntegrationCROCustomer ServiceClinical ResearchMicrosoft ExcelPowerpointVeterinary MedicineLeadershipOutlookMicrosoft OfficeGood Clinical Practice (Gcp)CRO ManagementAnimal Models

ABOUT CYNTHIA BETROS

Results-driven clinical research professional with 15+ years of experience in global clinical trial management, specializing in oncology and non-oncology studies across Phases 1–4. Proven record of supervising cross-functional teams, streamlining trial start-up, driving performance metrics, and fostering cross functional and external stakeholder collaboration. Expert in GCP/ICH compliance, regulatory inspections, and process improvement initiatives. Recognized for proactive problem-solving, innovation, and consistently exceeding operational goals in fast-paced environments.

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Cynthia Betros — Senior Clinical Trial Manager at Bristol Myers Squibb in Trenton, NJ, US | Unifers