CLINICAL RESEARCH ASSOCIATE I

<p>As a Clinical Research Associate you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications.&#xa0; You will build and maintain relationships with clinical sites and investigators.&#xa0; You will focus on subjects’ rights, safety and well-being and quality of data compliance.</p><p><strong>You will:</strong></p><ul><li>Conduct and report all types of onsite monitoring visits</li><li>Be involved in study startup (if applicable)</li><li>Perform CRF review, source document verification and query resolution</li><li>Be responsible for site communication and management</li><li>Be a point of contact for in-house support services and vendors</li><li>Communicate with internal project teams regarding study progress</li><li>Participate in feasibility research</li><li>Support regulatory team in preparing documents for study submissions</li></ul> <ul><li>College/University degree in Life Sciences or an equivalent combination of education, training &amp; experience</li><li>Experience as a Study Coordinator (or similar role)&#xa0;is required</li><li>Experience working on&#xa0;Gastroenterology clinical trials&#xa0;preferred&#xa0;</li><li>Full working proficiency in English</li><li>PC skills to be able to work with MS Word, Excel and PowerPoint</li><li>Ability to plan, multitask and work in a dynamic team environment</li><li>Communication, collaboration, and problem-solving skills</li><li>Ability and willingness to travel frequently&#xa0;</li><li>Valid driver’s license</li></ul> <p>Become a full-fledged clinical research professional with the support of a knowledgeable and professional team. &#xa0;You will develop a variety of skills while progressing with the company and contributing to our full-scale challenging projects.</p><p>For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.</p>