Manage clinical trial sites and protocol compliance across study phases, conducting monitoring visits, supporting site performance and recruitment, and partnering with investigators and internal teams.
Oversee clinical quality activities across assigned trials, supporting risk-based quality management, supplier oversight, and regulatory inspection readiness from preparation through follow-up.
Senior Director providing strategic Clinical Science leadership across infectious disease studies, programs, and assets, shaping development strategy, scientific standards, data interpretation, and team capability.
Lead and develop a field-based medical affairs team, overseeing scientific engagement, disease-state plans, research initiatives, performance, compliance, and project execution.
Provide strategic Clinical Science leadership across Immunology studies, programs, and assets, shaping development strategy, scientific standards, data interpretation, and cross-functional decisions.
Provide strategic Clinical Science leadership across pulmonary hypertension and cardiovascular programs, guiding study design, data interpretation, portfolio decisions, scientific standards, and team development.
Provide strategic Clinical Science leadership across vaccine studies, programs, and assets, shaping development strategy, scientific standards, data interpretation, and cross-functional decisions.
Lead therapeutic-area strategy and delivery for digital health technology across clinical studies, overseeing system lifecycles, data integration, compliance, service providers, and capability building.
Leads multi-team, multi-region Digital Health Technology delivery, overseeing clinical study systems, data integration, compliance, service providers, organizational strategy, and team development.
Execute risk-based financial, operational, SOX 404, IT, and process audits, documenting findings and helping strengthen internal controls across the Company.
Lead statistical programming for complex late-stage oncology development, delivering validated analyses and regulatory submissions while coordinating global programming teams and collaborating with project stakeholders.
Manage and develop a team of 6–14 Clinical Research Associates, supporting consistent trial monitoring, site performance, regulatory compliance, and effective resource planning.
Lead and develop field medical professionals, translating medical strategy into compliant scientific engagement, measurable team goals, and actionable insights across Pulmonary Hypertension.
This role will be key to ensure strong monitoring in our clinical trials, managing a team of Clinical Research Associates to ensure excellent study performance and compliance.
Lead enterprise clinical data programming and reporting strategy, overseeing complex study delivery, service providers, standards, and data engineering initiatives across therapeutic areas.
Leads study data programming and reporting strategy, delivery, and team development across therapeutic areas, advancing scalable standards, automation, data integrity, and regulatory-compliant execution.
Lead cross-functional drug and vaccine value and implementation projects, developing integrated strategies and plans while coordinating stakeholders, managing risks, and improving project processes.
The Specialist in Clinical Data Management is responsible for executing Quality Control Testing and User Acceptance Testing for electronic data capture systems and clinical databases.
The Payment Specialist will manage contract reviews, initiate site payments, and ensure compliance with accounting procedures while providing excellent customer service.
This role is responsible for ensuring compliance and performance for clinical trial contracts and budgets, while collaborating with various stakeholders to meet project timelines.
The Specialist, Engagement Operations Coordinator supports patient engagement initiatives by coordinating operational activities, ensuring compliance, and facilitating stakeholder interactions.
We are seeking a Growth and Improvement minded Regional Medical Scientific Director (aka Medical Science Liaison, MSL) in Inflammatory Bowel Disease Immunology that can help drive our Strategic Operating Priorities.
The Senior Scientist, Device Design Control Lead is essential for leading design control efforts in combination product development and ensuring high-quality product delivery.
We are seeking an accomplished scientific leader to join the Quantitative Pharmacology and Pharmacometrics – Immuno-Oncology (QP2‑IO) team as Senior Director, Advanced Pharmacometrics.
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