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.
In-House Clinical Research Associate, Poland
🕒 March 18
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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
• Support and observe clinical site monitoring services inhouse • Provide monitoring and site management activities for full-service studies assessing for protocol, SOP and regulatory compliance. • Conduct remote data review, support data query and closure activities, support Risk Based Monitoring (RBM) activities, assess data collection and (regulatory) document collection • Perform remote activities for investigational sites in accordance with corporate, sponsor and regulatory (ICH GCP and other) standards and guidelines • Maintain collaborative relationships with stakeholders.
🎯 Requirements
• Undergraduate university degree (Bachelor or Honors Bachelor) • 1-3 years' related experience with initial and On-going training.
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