
5001 - 10000 employees
Founded 1973
🏥 Healthcare
đź’Ľ Consulting
📦 Logistics
đź’° Private Equity Round on 2019-10
Healthcare • Consulting • Logistics
Clario is a company specializing in accelerating clinical trials from initiation to implementation through advanced technologies and services. Since 2018, Clario has revolutionized endpoint analyses in clinical trials by integrating over 30 artificial intelligence-enabled solutions across more than 600 active trials, enhancing data quality and patient privacy while expediting data collection processes. Clario provides a comprehensive clinical trial management platform, offering solutions such as eCOA, cardiac safety, medical imaging, precision motion, and respiratory services in various therapeutic areas including oncology, cardiology, and neurology. Known for its global reach, Clario supports clinical trials in over 100 countries with a strong focus on decentralized and hybrid trial models. The company's commitment to patient safety and innovation is reflected in their over 26,000 trials and involvement in numerous new drug approvals.
🔥 5 minutes ago
🇺🇸 United States – Remote
⏰ Full Time
đźź Senior
🏥 Clinical Operations
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5001 - 10000 employees
Founded 1973
🏥 Healthcare
đź’Ľ Consulting
📦 Logistics
đź’° Private Equity Round on 2019-10
Healthcare • Consulting • Logistics
Clario is a company specializing in accelerating clinical trials from initiation to implementation through advanced technologies and services. Since 2018, Clario has revolutionized endpoint analyses in clinical trials by integrating over 30 artificial intelligence-enabled solutions across more than 600 active trials, enhancing data quality and patient privacy while expediting data collection processes. Clario provides a comprehensive clinical trial management platform, offering solutions such as eCOA, cardiac safety, medical imaging, precision motion, and respiratory services in various therapeutic areas including oncology, cardiology, and neurology. Known for its global reach, Clario supports clinical trials in over 100 countries with a strong focus on decentralized and hybrid trial models. The company's commitment to patient safety and innovation is reflected in their over 26,000 trials and involvement in numerous new drug approvals.
• Provide leadership and oversight for global clinical study management and project delivery • Evaluate study progress, resource allocation, and team workload, implementing adjustments and mitigation strategies • Identify, assess, and mitigate risks across assigned programs and studies • Manage escalations and resolve operational, client, and project challenges • Support Clinical Project Managers in client communications regarding study status, risks, timelines, and deliverables • Lead cross-functional collaboration with internal and external stakeholders • Coordinate and facilitate routine status meetings • Serve as Project Manager for assigned studies, including start-up, execution, and closeout activities • Guide study teams across Therapeutic Areas and programs • Partner with senior leadership to prioritize deliverables, address resource needs, and communicate critical project updates • Drive operational excellence through continuous process improvement initiatives • Lead departmental initiatives, including planning, execution, communication, training, and progress reporting • Serve as a Therapeutic Area and/or Imaging Lead for operational readiness and implementation of new processes and procedures • Monitor operational challenges and recommend solutions to improve study delivery, quality, and efficiency • Coach, mentor, and develop Project Management team members • Support onboarding and training of new team members • Manage team assignments and workload distribution • Establish, maintain, and enforce departmental standards, SOP compliance, and study management best practices • Review and update project management and therapeutic team procedures • Perform additional duties, assignments, and special projects as required
• Bachelor's degree in Life Sciences, Pharmacy, Nursing, or a related discipline required; Master's degree preferred • 5-10 years of clinical research experience within a CRO, pharmaceutical, biotechnology, or related clinical development environment, including significant project management responsibility • Previous people management and leadership experience within clinical development, clinical operations, or clinical trial management • Strong knowledge of clinical trial processes, project management methodologies, and drug development practices • Working knowledge of Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, and FDA regulations • Experience supporting global clinical studies and leading cross-functional, geographically dispersed teams • Medical Imaging experience preferred • Demonstrated ability to coach, mentor, and develop team members • Strong organizational, prioritization, problem-solving, and decision-making skills • Excellent verbal and written communication skills, including the ability to effectively communicate in English with internal and external stakeholders • Proficiency with Microsoft Office applications and project management tools • Detail-oriented with the ability to manage multiple priorities and adapt effectively to changing business needs • Valid passport and ability to travel up to 20% as needed
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