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Lead the clinical development strategy and plan for Potravitug, including global late-stage trials, regulatory interactions, clinical documentation, and medical oversight. Partner with global cross-functional teams, investigators, and key opinion leaders to deliver high-quality studies and support publications, business development, registration, and launch.
Lead scientific work across research projects and author, review, and finalize client deliverables such as protocols, reports, analysis plans, evidence dossiers, presentations, and manuscripts. Manage project scope, timelines, budgets, and staffing; engage with clients; mentor junior staff; and contribute to proposals, conferences, training, recruitment, and regulatory meeting preparation.
The manager leads and executes clinical informatics projects, focusing on EHR policy development, workflow standardization, and enterprise-wide assessment of AI-enabled tools. This role acts as a bridge between clinical operations, quality and safety teams, and IT leadership to ensure efficient and safe healthcare delivery.
You will monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocols, SOPs, and regulatory standards. Additionally, you will coordinate study setup activities including identifying investigators and preparing regulatory submissions.
You will monitor and manage the progress of clinical studies at investigative sites to ensure compliance with protocols, SOPs, and regulatory standards. Additionally, you will coordinate study setup activities, including identifying investigators and preparing regulatory submissions.
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The Senior Clinical Research Associate conducts independent site monitoring visits to ensure clinical trial protocol compliance and data integrity. They also provide leadership, guidance, and oversight to the CRA team while managing study-related documentation and site relationships.
Analyze and interpret next-generation sequencing data for rare disease diagnostics while applying evidence-based clinical standards. Collaborate with multidisciplinary teams to uphold regulatory standards and contribute to the development of clinical interpretation services.
The Global Medical Director will provide clinical leadership and strategic guidance across the lifecycle of electrophysiology and LAAC therapies. They will collaborate with cross-functional teams to oversee clinical trials, ensure patient safety, and represent the company to regulatory authorities and key opinion leaders.
The Senior Director will define and execute the commercial strategy for the EMEA Clinical Sequencing business to achieve revenue and profitability targets. They will lead a diverse team, manage strategic customer relationships, and collaborate across divisions to drive market growth and operational excellence.
The Utilization Management Nurse Consultant reviews and assesses clinical information to support coverage determinations and applies clinical guidelines to ensure members receive appropriate care. They collaborate with providers and care teams to coordinate treatment plans and identify opportunities to enhance quality and efficiency.
Conduct and oversee clinical trial site monitoring, including site visits, source data verification, regulatory document review, investigational product accountability, and adverse event reporting. Guide and mentor CRA colleagues, support study planning and site issue resolution, and ensure compliance with protocols, ICH GCP, regulations, and applicable SOPs.
Review clinical cases and apply evidence-based guidelines to make coverage determinations and coordinate appropriate treatment. Collaborate with providers and stakeholders to improve care quality and ensure members receive the right care at the right time.
The Medical Monitor provides daily medical oversight for clinical trials to ensure patient safety, data integrity, and protocol compliance. They collaborate with cross-functional teams to manage safety signals, evaluate eligibility, and support regulatory submissions.
Lead and coordinate clinical site management activities from study startup through closeout while ensuring quality, compliance, and operational excellence. Partner with project management and cross-functional teams to drive study performance, mitigate risks, and support site recruitment strategies.
You will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. This involves conducting site visits, collaborating with cross-functional teams, and providing training to site staff to ensure successful trial execution.
The OT Systems Subject Matter Expert will serve as the technical authority for operational technology, defining standards and reference architectures for AI factory power and cooling systems. They will lead OT design reviews, oversee commissioning, implement cybersecurity frameworks, and manage vendor relationships to ensure system availability and security.
The Technical Specialist will review and evaluate medical device technical and clinical documentation to ensure compliance with regulatory standards. They will also manage certification activities for a portfolio of manufacturers and provide specialist regulatory support to the business.
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Design and validate realistic medical tasks to evaluate the performance of AI agents in interpreting clinical information and healthcare workflows. Collaborate with technical teams to establish objective evaluation criteria and reference solutions based on scientific evidence.
The Clinical Demand Specialist will manage account profiling and develop relationships with key healthcare stakeholders to drive PCT testing strategies. They will also deliver educational programs and represent the company at professional meetings to meet annual growth targets.
You will oversee Good Clinical Practice compliance across sponsored and partner studies, managing deviations, CAPAs, and quality reviews. You will also collaborate with data and clinical teams to ensure data integrity and system qualification throughout the study lifecycle.
The consultant will lead medical process analysis and facilitate stakeholder sessions to translate Medical Affairs needs into clear workflows and business requirements. They will also support the transition to Vault CRM by identifying gaps, documenting dependencies, and coordinating with system owners.
The RN Care Manager conducts comprehensive clinical assessments and develops individualized care plans for patients with complex conditions. They lead multidisciplinary teams to coordinate care, manage transitions, and ensure continuity while advancing value-based care goals.
The Senior CRA conducts site monitoring visits and provides leadership to ensure clinical trials adhere to protocol, SOPs, and regulatory requirements. They also manage study budgets, facilitate site training, and collaborate with cross-functional teams to resolve data and site-related issues.
The Senior CRA conducts independent site monitoring visits and provides leadership to ensure clinical trial compliance and quality. They manage site relationships, review monitoring reports, and collaborate with cross-functional teams to resolve study-related issues.
The Senior Strategic Healthcare Partner builds trusted relationships with healthcare professionals and institutions to identify care gaps and co-create solutions that improve patient access and system sustainability. The role involves collaborating across functions to translate system insights into quality-improvement initiatives while maintaining a non-promotional mandate.
You will assist senior biostatisticians with clinical study support, including study design, sample size calculations, and data analysis. Additionally, you will be responsible for writing statistical analysis plans, developing data manipulation programs, and preparing statistical summary reports.
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The Senior Biostatistician will lead biostatistics tasks for clinical studies, including the development of statistical analysis plans and reporting specifications. They are responsible for performing statistical analyses, interpreting complex medical data, and contributing to bid defense meetings.
The Associate Director/Director will contribute to the development of European medical strategies and tactics while driving excellence in medical activities across country teams. They will also provide actionable insights, monitor KPIs, and support cross-functional initiatives to ensure launch readiness and effective stakeholder engagement.
The VP of Clinical Solutions Content oversees the global publishing program, including medical reference and digital content portfolios. They are responsible for driving content strategy, optimizing financial performance, and fostering innovation across global and local markets.
The VP of Clinical Solutions Content oversees the global publishing program, including medical reference books and digital content creation. They are responsible for driving content strategy, optimizing financial performance, and ensuring effective platform integration across the business unit.
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