Clinical Research Associate-Medical Device This Jobot Job is hosted by Audrey Block. Are you a fit? Easy Apply now by clicking the "Easy Apply" button and sending us your resume. Base pay range: $100,000.00/yr - $140,000.00/yr A Bit About Us: We are a well-established consulting firm that provides solutions to medical device companies, pharmaceuticals, and biologics. We are hiring a CRA with medical device experience to join our team! Why join us? Opportunity to wear different hats in a small company - lots of growth! People management if interested. Strong Benefits And Compensation Package. Opportunity to work in multiple therapeutic and diagnostic areas. Job Details: We are looking for an experienced Clinical Research Associate (CRA) with a focus on Medical Devices to join our dynamic and innovative scientific team! Responsibilities: Planning and conducting clinical studies of medical devices to ensure they are safe and effective. Monitoring clinical trials, ensuring they are carried out in accordance with the study protocol, standard operating procedures, good clinical practice (GCP), and the applicable regulatory requirements. Coordinating with investigators and site staff to ensure the quality and integrity of the data collected in clinical trials. Preparing and presenting study documentation including protocols, case report forms, and study reports. Assisting in the development of study budgets and timelines. Conducting site initiation, interim monitoring, and close-out visits. Ensuring that adverse events and other clinical issues are reported promptly and accurately. Participating in the preparation of regulatory submissions. Liaising with internal and external stakeholders to ensure smooth execution of studies. Qualifications: A Bachelor’s degree in a scientific or healthcare discipline. A minimum of 2 years of experience in monitoring clinical studies, with medical device experience. Thorough knowledge and understanding of ICH guidelines, GCP, and relevant regulatory requirements. Excellent communication and interpersonal skills, with the ability to interact effectively with team members, investigators, and site staff. Strong organizational skills, with the ability to manage multiple tasks and meet deadlines. Proficient in Microsoft Office Suite and clinical trial management systems. Ability to travel as required for site visits. If you are a motivated professional with a passion for improving patient care through scientific innovation, we invite you to apply. Join us and contribute to the development and delivery of next-generation medical devices. Interested in hearing more? Easy Apply now by clicking the "Easy Apply" button. Seniority level Entry level Employment type Full-time Job function Research, Analyst, and Information Technology Industries Biotechnology Research, Research Services, and Nanotechnology Research #J-18808-Ljbffr Jobot
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