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You will lead end-to-end digital transformation projects for energy sector clients, focusing on IT/OT architectures and grid operations. Additionally, you will contribute to the growth of the energy consulting portfolio and strengthen client relationships.
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.
The Utilization Management Nurse Consultant assesses and coordinates healthcare services by applying clinical criteria to render coverage determinations. They collaborate with providers to facilitate appropriate care and identify opportunities to improve the quality and effectiveness of benefit utilization.
Deliver personalized lessons on occupational health and safety while helping students understand workplace regulations and risk assessment. Adapt teaching materials to individual student needs to foster practical knowledge and confidence.
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The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They are responsible for verifying informed consent, managing clinical data integrity, and overseeing investigational product handling at assigned sites.
The Head of Clinical Delivery provides strategic governance and oversight of clinical coaching to ensure consistency, quality, and regulatory compliance across the benefit area. The role involves leading the quality function, managing clinical teams, and engaging with external stakeholders like the DWP to drive continuous improvement.
The Head of Clinical Delivery provides strategic governance and oversight of clinical coaching, ensuring standards and consistency across the benefit area. They lead the end-to-end quality function, manage clinical teams, and engage with external stakeholders to drive performance and clinical integrity.
The Health System Navigator helps participants overcome health, social, and environmental barriers to employment by facilitating connections with local services and community partners. They also track participant progress, maintain accurate service maps, and provide intelligence to support continuous service improvement.
You will support the management of clinical trial sites by conducting monitoring activities, ensuring protocol adherence, and maintaining essential trial documentation. Additionally, you will collaborate with cross-functional teams to ensure data quality, patient safety, and inspection readiness.
You will act as the primary HSSE contact for colleagues and subcontractors, conducting weekly audits and safety inspections on construction sites. Additionally, you are responsible for performing risk assessments, managing emergency protocols, and ensuring compliance with environmental and safety regulations.
The Clinical Research Associate will conduct site monitoring visits, including initiation and close-out, to ensure protocol compliance and data quality. They will also act as the primary point of contact for site personnel and support regulatory submissions and risk assessment activities.
The Medical Science Liaison will lead scientific exchanges with hematologists and oncologists while developing long-term relationships with key external experts. They are responsible for facilitating clinical trials, providing medical expertise to internal teams, and ensuring compliance with regulatory standards.
The A&G Clinical Specialist manages clinical case development and resolution for member complaints, grievances, and appeals while ensuring compliance with regulatory standards. They are responsible for researching issues, interpreting health plan policies, and preparing cases for Medical Director review or external appeal processes.
The Pipeline Medical Science Liaison will build scientific relationships with investigators and healthcare professionals to shape the dialogue around neuroscience and psychiatry pipelines. They will also support clinical development programs by identifying study sites and translating scientific evidence into actionable insights for R&D and Medical Affairs.
The Medical Physicist will support IBA teams and customers with the acceptance, commissioning, and validation of proton therapy equipment. They are responsible for providing on-site and remote technical support, training customers, and delivering structured product feedback to internal teams.
The Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites in compliance with SOPs, GCP, and ICH guidelines. They ensure subject safety and data integrity by reviewing documentation and managing investigational products.
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The Medical Science Liaison will build and maintain scientific relationships with healthcare professionals and oncology centers to facilitate evidence-based exchange. They will also gather medical insights to inform strategy and support evidence-generation activities like investigator-sponsored studies.
The role involves assisting with the preparation, documentation, and maintenance of clinical trial records, including the Trial Master File and Case Report Forms. You will collaborate with clinical teams to ensure accurate data flow, site compliance, and effective communication across research projects.
The Medical Science Liaison acts as a scientific expert for prostate cancer, implementing medical affairs plans and building partnerships with external experts. They coordinate clinical study activities, manage medical education initiatives, and provide scientific insights to support patient-centered solutions.
Provide clinical and technical support for electrophysiology procedures and promote the use of Abbott products. Initiate customer training, manage troubleshooting, and represent the organization at national congresses.
The Regional Clinical Manager is responsible for leading a clinical team, managing strategic and tactical operations, and ensuring the delivery of high-quality patient care. This role involves frequent field travel to provide coaching, manage clinical outcomes, and support customer communication and implant procedures.
Build and maintain scientific partnerships with healthcare professionals, key opinion leaders, clinical sites, and other stakeholders across East Germany, providing accurate, non-promotional medical information on BeOne’s oncology products and pipeline. Gather and communicate medical insights, support clinical research and evidence generation, and collaborate with Medical Affairs and cross-functional teams to plan and deliver regional medical strategies and activities.
Conduct site qualification, initiation, monitoring, and close-out visits while ensuring protocol compliance, data integrity, and patient safety. Collaborate with investigators and site staff, review clinical data and resolve queries, and contribute to study documentation, protocols, and clinical study reports.
You will lead complex SAP S/4HANA transformation projects for healthcare clients, overseeing the entire bid process and solution design. Additionally, you will provide professional guidance to the Atos SAP team and manage relationships with key stakeholders and decision-makers.
The Clinical Specialist provides technical support to surgical and operating room staff during procedures and drives commercial sales activities for navigation, imaging, and robotics portfolios. They are responsible for training hospital staff on device application and coordinating case support with account sales representatives.
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Provide clinical support and consultation to medical staff during electrophysiological procedures using the CARTO 3 navigation system. Act as the primary point of contact for technical troubleshooting and drive the adoption of the product portfolio within clinical labs.
Manage day-to-day clinical trial operations, ensuring adherence to timelines, budget, and quality standards. Collaborate with cross-functional teams and stakeholders to implement protocols and ensure regulatory compliance.
The Senior Director is responsible for leading complex healthcare technology engagements, specifically focusing on MEDITECH implementations, migrations, and optimization programs. They serve as a trusted advisor to client executives while directing project teams to ensure successful delivery and business growth.
The Clinical Trial Manager is responsible for site management oversight, clinical monitoring, and ensuring protocol, GCP, and regulatory compliance. They coordinate study milestones, manage project risks, and oversee the performance of CRAs and Central Monitors to ensure data integrity and patient safety.
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