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Provide clinical and sales support by educating customers and providing technical procedure coverage for Structural Heart products. Train interventional cardiologists and catheter lab staff on the use of stroke prevention technologies.
Provide clinical and sales support by educating customers and providing technical assistance to physicians during Structural Heart procedures. Collaborate with Territory Managers to ensure positive patient outcomes and implement product marketing strategies.
Provide clinical and sales support by educating customers and providing technical procedure coverage for Stroke Prevention products. Train interventional cardiologists and catheter lab staff on the proper use of Structural Heart devices.
Provide clinical and sales support by educating customers and providing technical procedure coverage for Structural Heart products. Train interventional cardiologists and catheter lab staff on the proper use of stroke prevention devices.
Provide clinical and sales support by educating customers and providing technical procedure coverage for Structural Heart products. Train interventional cardiologists and catheter lab staff on the use of stroke prevention technologies.
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Provide clinical and sales support by educating customers and providing technical procedure coverage for Structural Heart products. Train interventional cardiologists and catheter lab staff on the use of stroke prevention devices.
Provide clinical and sales support by educating customers and providing technical assistance to physicians during Structural Heart procedures. Collaborate with Territory Managers to ensure positive patient outcomes and implement product marketing strategies.
Provide clinical and sales support by educating customers and providing technical assistance to physicians during Structural Heart procedures. Collaborate with Territory Managers to ensure positive patient outcomes and implement product marketing strategies.
Manage clinical trial operations including site identification, regulatory compliance, and the development of essential study documents. Oversee project timelines, vendor contracts, and multidisciplinary teams to ensure high-quality project deliverables.
Oversee clinical operations management for industry-sponsored trials, including defining project scope, timelines, and deliverables from initiation to close-out. Manage multidisciplinary teams and provide operational support for biostatistics, programming, and endpoint specialty services.
The Sr. Clinical Operations Manager serves as the primary contact for industry-sponsored clinical trials, overseeing project scope, timelines, and deliverables. They are responsible for managing site identification, regulatory compliance, vendor contracts, and mentoring other Clinical Operations Managers.
The role focuses on managing clinical investigator relationships and overseeing site-level strategies to ensure predictable enrollment and data delivery. It involves acting as a scientific ambassador to align investigators with protocol intent and optimizing trial conduct through data-informed insights.
Lead value, evidence, and outcomes initiatives to support evidence-based strategies across various products and healthcare settings. Act as a scientific expert to translate complex clinical and economic data into communications for internal and external stakeholders.
Define clinical standards and safety guardrails for AI-augmented primary care while building multi-agent architectures for clinical problem solving. Collaborate across interdisciplinary teams to translate clinical best practices into structured logic for grounding LLMs.
Lead the development, customization, and maintenance of Integrated Study Timelines (IST) for clinical trials using global templates. Collaborate with cross-functional teams to monitor project progress, identify critical path items, and communicate updates to stakeholders.
The role focuses on identifying and closing new business opportunities with regional and national healthcare payer clients to drive revenue growth. Responsibilities include managing the full sales cycle, developing strategic account plans, and aligning IQVIA's data and technology solutions with client needs.
Provide clinical and sales support by educating customers and providing technical assistance to physicians during Structural Heart procedures. Collaborate with Territory Managers to ensure positive patient outcomes and implement product marketing strategies.
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The role involves coordinating and monitoring clinical trial activities, including maintaining study documentation and ensuring cost efficiency. It also requires building collaborative relationships with investigators and ensuring strict compliance with regulatory requirements and patient safety.
Lead the development of medical writing strategies and deliverables, including protocols, CSRs, and regulatory submissions. Collaborate with cross-functional teams to analyze clinical trial data and mentor junior medical writers.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with informed consent and safety reporting requirements.
Coordinate the delivery of digital health projects and programs, providing technical expertise in specification development and supplier management. Lead cross-functional teams through scope changes and ensure inspection readiness for digital health technologies.
Responsible for site management oversight, clinical monitoring, and ensuring protocol and GCP compliance with a focus on patient safety and data integrity. The role involves managing clinical project teams, mitigating risks, and collaborating with functional leaders to meet study milestones.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Define and execute the market development strategy for Spatial Biology and Omics across Biopharma and academic segments. Drive qualified pipeline creation by translating complex scientific workflows into scalable commercial use cases and value propositions.
The VP of Medical Affairs will build and lead the Medical Affairs function, overseeing MSLs, medical communications, and investigator-sponsored trials for Orca-T. This role involves establishing relationships with key opinion leaders and collaborating with R&D and Commercial teams to support product launch and data promulgation.
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Provide strategic medical and scientific expertise in hematology-oncology to support proposal development, protocol design, and client engagements. Act as a subject matter expert throughout the research and development lifecycle to guide project teams and sponsors.
The Team Lead is responsible for maintaining Trial Master Files inspection readiness in compliance with SOPs, ALCOA principles, and industry regulations. They drive the delivery of project objectives and oversee TMF services for multiple studies while managing risks and KPIs.
Accountable for directing multiple oncology projects simultaneously to ensure delivery within cost, time, and quality requirements. Collaborates with cross-functional leadership to improve business processes and supports proposal development for new clients.
The role focuses on supporting client data onboarding and intake processes by partnering with vendors and internal teams. Key duties include communicating file requirements, tracking acquisition timelines, and resolving data-related issues to support value-based care strategies.
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