Alimentiv
201 - 500 employees
Founded 2020
⚕️ Healthcare Insurance
🔬 Science
💊 Pharmaceuticals
Healthcare Insurance • Science • Pharmaceuticals
Alimentiv is a specialty contract research organization focused on gastrointestinal (GI) and liver diseases. With over 30 years of experience, Alimentiv offers a comprehensive range of clinical research and imaging services, including clinical trial management, site management, regulatory affairs, and precision medicine. The company is at the forefront of medical research and development, providing state-of-the-art imaging solutions and actionable biomarker insights. Alimentiv supports the development of GI compounds and is active in more than 60 countries, working with a network of medical and operational experts to accelerate clinical trials and patient recruitment.
Clinical Operations Lead – Clinical Trial Manager
🔥 30 minutes ago
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Alimentiv
201 - 500 employees
Founded 2020
⚕️ Healthcare Insurance
🔬 Science
💊 Pharmaceuticals
Healthcare Insurance • Science • Pharmaceuticals
Alimentiv is a specialty contract research organization focused on gastrointestinal (GI) and liver diseases. With over 30 years of experience, Alimentiv offers a comprehensive range of clinical research and imaging services, including clinical trial management, site management, regulatory affairs, and precision medicine. The company is at the forefront of medical research and development, providing state-of-the-art imaging solutions and actionable biomarker insights. Alimentiv supports the development of GI compounds and is active in more than 60 countries, working with a network of medical and operational experts to accelerate clinical trials and patient recruitment.
📋 Description
• Responsible for the clinical operations of a project within a defined regional/global level • Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites • Acts as a primary liaison between the CRAs and the clinical project team • Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs, implementation of enrollment and recruitment strategies, preparation of the monitoring plan and other structural documentation and oversight of monitoring visit scheduling, site and monitoring performance metrics, issue escalation and corrective actions • Develop study tools for site and CRA use, review visit reports, track protocol deviations
🎯 Requirements
• College diploma/degree AND 7-9 years related experience +continuous training and knowledge/skills upgrading • Undergraduate university degree (Bachelors or Honors Bachelors) AND 4-6 years' experience + substantial ongoing job-related training • Minimum of 3 years CRA experience • Strong experience with EDC systems • Proficient with MS Office • Demonstrate proactive, detail-oriented, task-driven and highly organized attributes • Demonstrated ability in report writing and strong understanding of clinical research documents
🏖️ Benefits
• Accommodations for persons with disabilities are available on request • Health Sciences, Life Sciences or Nursing specialty preferred, or SoCRA and/or ACRP Certification/Designation
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