Raw description: "<p><strong>About the Job</strong></p><p>Join Excelya, where <strong>Audacity, Care, and Energy</strong> define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.</p><p>This role is an exciting opportunity to contribute to a dynamic, ambitious team in Cinical Operations. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.</p><p><strong>Main Responsibilities</strong></p><ul> <li>oordinate the local clinical team involved in national and international oncology trials. </li> <li> Participate in the development of study documents (protocols, ICFs, CRFs, etc.). </li> <li> Manage the study budget and timeline to ensure efficient execution. </li> <li> Oversee site and vendor selection, activation, and performance throughout the study. </li> <li> Ensure successful patient recruitment through coordinated clinical activities. </li> <li> Deliver study results with high quality, on time and within budget. </li> <li> Manage regulatory submissions and administrative follow-up in compliance with ICH-GCP and local regulations. </li> <li> Lead feasibility assessments and investigator selection. </li> <li> Provide transversal management and operational oversight of CRAs.</li> </ul><p><strong>Requirements</strong></p><p><strong>About You</strong></p><p>At Excelya, <strong>taking audacious steps is encouraged</strong>, so we’re looking for individuals who are ready to grow with us and share our values.</p><ul> <li> <strong>Experience:</strong> Proven ability to thrive in collaborative, fast-moving environments (avoid requiring minimum years—<strong>talent matters most to us!</strong>)</li> <li> <strong>Skills: </strong>Experience in clinical project management within the pharmaceutical industry or CRO, preferably on interventional international studies, Strong organizational, communication, and leadership skills.</li> <li> <strong>Education:</strong> Degree in Pharmacy, Life Sciences, or equivalent.</li> <li> <strong>Languages:</strong> Fluency in French & English</li> </ul><p><strong>Benefits</strong></p><p><strong>Why Join Us?</strong></p><p>At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.</p><p>Here’s what makes us unique—</p><p>We are a young, ambitious health company representing 900 Excelyates, driven to become Europe’s <strong>leading mid-size CRO </strong>with the <strong>best employee experience</strong>. Our <strong>one-stop provider service model</strong>—offering full-service, functional service provider, and consulting—enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient’s journey.</p><p><strong>Excelling with care</strong> means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.</p>\n"
<p><strong>About the Job</strong></p><p>Join Excelya, where <strong>Audacity, Care, and Energy</strong> define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.</p><p>This role is an exciting opportunity to contribute to a dynamic, ambitious team in Cinical Operations. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.</p><p><strong>Main Responsibilities</strong></p><ul> <li>oordinate the local clinical team involved in national and international oncology trials. </li> <li> Participate in the development of study documents (protocols, ICFs, CRFs, etc.). </li> <li> Manage the study budget and timeline to ensure efficient execution. </li> <li> Oversee site and vendor selection, activation, and performance throughout the study. </li> <li> Ensure successful patient recruitment through coordinated clinical activities. </li> <li> Deliver study results with high quality, on time and within budget. </li> <li> Manage regulatory submissions and administrative follow-up in compliance with ICH-GCP and local regulations. </li> <li> Lead feasibility assessments and investigator selection. </li> <li> Provide transversal management and operational oversight of CRAs.</li> </ul><p><strong>Requirements</strong></p><p><strong>About You</strong></p><p>At Excelya, <strong>taking audacious steps is encouraged</strong>, so we’re looking for individuals who are ready to grow with us and share our values.</p><ul> <li> <strong>Experience:</strong> Proven ability to thrive in collaborative, fast-moving environments (avoid requiring minimum years—<strong>talent matters most to us!</strong>)</li> <li> <strong>Skills: </strong>Experience in clinical project management within the pharmaceutical industry or CRO, preferably on interventional international studies, Strong organizational, communication, and leadership skills.</li> <li> <strong>Education:</strong> Degree in Pharmacy, Life Sciences, or equivalent.</li> <li> <strong>Languages:</strong> Fluency in French & English</li> </ul><p><strong>Benefits</strong></p><p><strong>Why Join Us?</strong></p><p>At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.</p><p>Here’s what makes us unique—</p><p>We are a young, ambitious health company representing 900 Excelyates, driven to become Europe’s <strong>leading mid-size CRO </strong>with the <strong>best employee experience</strong>. Our <strong>one-stop provider service model</strong>—offering full-service, functional service provider, and consulting—enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient’s journey.</p><p><strong>Excelling with care</strong> means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.</p>