Sr Clinical Operation Specialist / Lead Clinical Operation Specialist (immediate Joiner)<p>Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.<br><br>Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. <br><br>Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need. <br><br>Discover what your 25,000 future colleagues already know: </p><h3>Why Syneos Health</h3><p>• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.<br>• We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life. <br>• We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress. </p><h3>Job Responsibilities</h3><ul><li><h3>Job Responsibilities</h3></li><li><b>7–10 years of relevant CTA experience</b></li><li>CTA experience <b>combined with centralized monitoring</b> exposure is preferred</li><li><b>Home-based position</b> with <b>immediate joiners</b> strongly preferred</li><li>Strong <b>operational understanding of clinical research</b></li><li>Good communication skills and <b>fluency in English</b></li><li>Must be <b>proactive, resourceful, and a quick learner</b></li><li><h3>roles and responsibilities.</h3></li><li><h3>Support set-up and maintenance of information in Clinical Trial Management Systems and other systems as applicable, independent or under the responsibility of (Sr.) Clinical Project Manager as applicable: Update data, timelines, milestones, Ethics Committee /</h3></li><li><h3>Health Authority authorizations, etc. on an ongoing basis.</h3></li><li><h3>Support (Sr.) CPM with study budget management, ensuring accurate planning, tracking and reporting of clinical study budget and Grant Plan as applicable. Perform Good receipt booking in line with Vendor financial report and study sta