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The role involves providing scientific support for epidemiology studies, including literature reviews, data cleaning, and quality control. Additionally, the position requires operational coordination across multiple studies to ensure high-quality execution and timely delivery of scientific outputs.
The Clinical/Medical Scientist will develop medical plans and perform regular medical data reviews to identify risks and trends in infectious disease clinical trials. They will also serve as a primary interface between internal teams, customers, and vendors to ensure project milestones and quality deliverables are met.
The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure protocol and regulatory compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure protocol and regulatory compliance. They also manage site-level activities, verify clinical data accuracy, and support patient recruitment and retention strategies.
The Clinical Scientist collaborates with the Medical Director to develop medical plans and perform regular medical data reviews to identify risks and trends. They serve as the primary interface between internal teams and customers to ensure project milestones and data integrity are maintained.
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The nurse will provide health education to patients with various pathologies to promote healthy lifestyle changes. They will also conduct health surveys to collect data on patient well-being and medical history while maintaining high quality standards.
The Senior Clinical Research Associate is responsible for site qualification, initiation, monitoring, and study close-out visits to ensure clinical programs are executed with quality. They also provide mentoring to less experienced staff and ensure site compliance with protocols and data integrity.
The Medical Coding Specialist performs accurate and timely coding of clinical trial data, including adverse events and medical history, using MedDRA. They also collaborate with study teams to resolve coding queries and ensure data quality and consistency throughout the clinical development process.
The role involves conducting clinical trial monitoring activities, including site visits and ensuring protocol compliance and data integrity. You will also collaborate with investigators and site staff to facilitate study conduct and prepare essential study documentation.
The Clinical Research Associate is responsible for conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. They also collaborate with investigators to facilitate study conduct and perform data review to maintain high-quality clinical data.
The role involves ensuring the quality and timely submission of clinical trial data and managing regulatory and ethical documentation. You will also perform site identification activities and maintain site-related documentation within the Trial Master File.
The Clinical Application Specialist will support neurosurgical clinical programs by training personnel on the Neuro Exablate system and participating in brain indication treatments. They will also analyze treatment results, contribute to product development, and collaborate with regional teams to optimize the lifecycle of clinical centers.
The role involves managing Spain's occupational risk prevention requirements and the Internal Prevention Service while providing global HSE guidance. You will lead cross-functional projects, conduct risk assessments, and manage vendor relationships to ensure compliance and safety standards.
Responsible for site management oversight, clinical monitoring, and central monitoring deliverables to ensure patient safety and regulatory compliance. Collaborates with functional leaders to meet study milestones and manages clinical project team performance and risk mitigation.
Provide medical guidance and advice to patients with complex health needs through telematic means. Manage medical resources, perform clinical triage, and ensure accurate documentation of patient cases in the system.
The Clinical Development Lead will architect and execute global clinical strategies for the toxicology and drug testing portfolio to drive diagnostic innovation. They will also lead high-stakes interactions with regulatory bodies and integrate real-world evidence to support product registration and market adoption.
The Clinical Success Manager will demo, install, and train clinics on automation software while proactively managing customer relationships and feedback. They will also collaborate with the sales team to support prospective customers and develop training materials to improve clinical efficiency.
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The Senior Clinical Trial Coordinator provides administrative and technical support to project teams while overseeing assigned clinical trial activities. They act as a cross-functional liaison, manage study documentation, and ensure project tasks are completed on time and within budget.
The Senior Director will oversee clinical monitoring strategies, manage protocol execution risks, and ensure quality compliance across clinical operations. They will also support commercial activities, including proposal development and bid defense meetings, while collaborating with internal and external stakeholders.
The Clinical Project Leader is responsible for leading cross-functional teams to deliver clinical trials on time, within budget, and in compliance with ICH GCP standards. They manage client relationships, project P&L, risk mitigation, and ensure high-quality project deliverables.
The trainee will be responsible for drafting scientific texts and preparing internal materials for the pharmaceutical industry. They will also participate in advisory boards and other departmental tasks.
The Senior Medical Director provides medical oversight and monitoring for oncology and hematology clinical trials while ensuring scientific credibility and regulatory compliance. They also partner with business development to support growth through bid strategy, proposals, and building relationships with key opinion leaders.
The Centralized Monitoring Analyst is responsible for setting up and programming the Centralized Monitoring platform, including QTLs, KRIs, and data visualizations. They also support the Centralized Monitoring Lead in developing study-specific strategies and maintaining platform specifications.
The Clinical Project Leader is responsible for leading cross-functional teams to deliver clinical trials on time, within budget, and in compliance with ICH GCP standards. They manage client relationships, project plans, risk mitigation, and financial performance including revenue recognition and forecasting.
The Senior Manager will lead global Medical Affairs strategies, fostering partnerships with Key Opinion Leaders and managing scientific evidence generation. They will also provide medical leadership throughout the product lifecycle and ensure all communications comply with regulatory and ethical standards.
The Senior Clinical Trial Manager provides leadership and direction to clinical site management teams while overseeing regional CTMs and coordinating study activities. They are responsible for developing monitoring strategies, managing budgets, and ensuring compliance with clinical protocols and regulatory requirements.
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The Medical Director will provide expert medical guidance to project teams and ensure clinical studies adhere to ethical and legal standards. They will also oversee safety data reviews, contribute to study documentation, and support business development efforts.
The Clinical Trial Manager will oversee individual oncology clinical trials, managing external vendors, study documentation, and site monitoring activities. They are responsible for ensuring regulatory compliance, coordinating study supplies, and providing leadership to Clinical Research Associates.
The Senior Clinical Scientist will design and conduct clinical studies to evaluate the safety and efficacy of innovative treatments while providing strategic leadership for clinical programs. They will also author clinical protocols, study reports, and regulatory submissions in collaboration with cross-functional teams.
The Manager Clinical Operations oversees, trains, and coaches a team while managing performance through metrics and key performance indicators. They also collaborate with leadership on resourcing, ensure adherence to regulatory standards, and support project deliverables.
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