Business Area: Strategic Solutions Remote Working: Office Based Job Description As an In-House Clinical Research Associate (IHCRA), you will be joining the world's largest and most comprehensive clinical research organization, powered by healthcare intelligence. You will be partnering with one of our global pharmaceutical clients; a company that is advancing the development of new medicines, biologic therapies, and vaccines for many of the world's most challenging diseases including cancer, cardio-metabolic diseases, Alzheimer's, and infectious diseases. Be ready to work in a solid partnership and an environment driven by innovation and continuous improvement. What you will be doing: An In-House CRA (IHCRA) is a critical role as in-house CRAs work independently in the field and are the face of the company in the investigative site community. They are also critical as they represent the customer in the prescribing community. In-house CRAs are responsible for ensuring that patients' rights and safety are protected and that clinical trials are conducted per regulations and the protocol. Performs investigator recruitment activities utilizing phone scripts, questionnaires, study site materials, and other tools for use in evaluating investigative sites. Utilizes the Clinical Trial Management System (CTMS) to ensure investigator recruitment activities are accurately tracked. Performs essential document collection, review, maintenance, and close-out activities, ensuring that sponsor and investigator obligations are being met and are in compliance with applicable local regulatory requirements and ICH/GCP guidelines. Supports investigators and investigative staff in fulfilling obligations with regard to local submissions according to local regulatory and Institutional Review Board (IRB)/Independent Ethics Committee (IEC) requirements. Performs study tracking via the CTMS or Sponsor designated system to ensure that the study files are current, accurate, and complete. Documents site and Sponsor contact and study interactions in a timely and professional manner. You are: Experience with PC-Windows, word processing, and electronic spreadsheets required. Knowledge of local regulatory authority drug research and development regulations required. Clinical trials support or pharmaceutical industry experience required. What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work-life balance opportunities for you and your family. At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we've done to become a more inclusive organization. We're dedicated to providing an inclusive and accessible environment for all candidates. Impactful work. Meaningful careers. Quality rewards. At ICON, our employees are our greatest strength. That's why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is to lead a global team, become a deep scientific or technical expert, work in-house with our customers, or gain experience in a variety of different ICON functions, we will support you in realizing your full potential. #J-18808-Ljbffr