
5001 - 10000 employees
Founded 1973
đ„ Healthcare
đŒ Consulting
đŠ Logistics
đ° Private Equity Round on 2019-10
Healthcare âą Consulting âą 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.
đ„ 3 minutes ago
đșđž United States â Remote
â° Full Time
đĄ Mid-level
đ Senior
đŠ H1B Visa Sponsor
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5001 - 10000 employees
Founded 1973
đ„ Healthcare
đŒ Consulting
đŠ Logistics
đ° Private Equity Round on 2019-10
Healthcare âą Consulting âą 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.
âą Interpret clinical data in accordance with standard medical practice, Good Clinical Practice (GCP) guidelines, study protocols, charters, and Clario SOPs âą Accurately and timely complete source documents and Case Report Forms (CRFs) in line with protocol and charter requirements âą Correct documentation entries as required, ensuring traceability and compliance âą Participate in protocol-specific training sessions and onboarding activities âą Perform Photo Image Quality Assessment (Photo IQA) and participate in the medical photography process âą Review study protocols, charters, and associated clinical and technical documentation âą Ensure the security, confidentiality, and integrity of images, data, equipment, study protocols, and subject information âą Participate in sponsor site visits, audits, and inspections as requested âą Collaborate with management to identify, troubleshoot, and resolve oncology study issues âą Maintain responsibility for ongoing professional education and medical competency âą Perform quality control checks on assigned work for completeness and accuracy âą Identify opportunities for and participate in continuous performance improvement initiatives âą Contribute to the development, review, and evaluation of SOPs and study-specific procedures âą Create test cases and support oncology-specific training initiatives âą Participate in the Medical Affairs lecture series âą Maintain a safe work environment and report workplace hazards promptly âą Perform additional duties as assigned by the Chief Medical Officer, VP of Medical Oncology, or Senior Medical Director
âą Medical degree (MD or equivalent) required âą Board-Certified Oncologist âą Graduate of an approved oncology training program; subspecialty training as applicable âą Valid U.S. medical license preferred âą Experience in clinical research and/or imaging core lab environments preferred âą Comprehensive understanding of treatment response evaluation for solid tumors and hematologic malignancies âą Strong organizational and time-management skills with the ability to manage multiple projects concurrently âą Self-motivated, flexible, and adaptable to evolving business needs âą Strong interpersonal and communication skills with a professional, collaborative demeanor âą Analytical skills to effectively interpret diagnoses, radiographic assessments, and oncology treatment outcomes
âą Competitive compensation aligned to the U.S. market âą Comprehensive health, retirement, and wellness benefits âą Opportunities to work on global oncology clinical trials âą Collaboration with multidisciplinary medical, scientific, and operational teams âą Ongoing professional development and continuing medical education support
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