Sr. Project Specialist based in South Korea Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. 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 accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health • 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. • We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. • We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.

• Ensure safe and effective operations of clinical research studies, including the implementation of advanced methodologies and technologies to enhance study outcomes • Safeguard the wellbeing of research subjects in a medical capacity, ensuring adherence to ethical standards and best practices in patient care • Review study protocols and execute procedures in alignment with protocols and regulatory, health, and safety standards, including the development of risk mitigation strategies and compliance monitoring • Raise or escalate study issues as necessary, providing detailed analysis and recommendations for resolution • Recruit and coordinate communication with clinical trial volunteers and patients, utilizing innovative recruitment strategies and maintaining clear and consistent communication throughout the study • Follow applicable regulations globally and by region, ensuring all activities are compliant with local and international guidelines • Collaborate with cross-functional teams to develop study materials, including the creation of comprehensive training programs and resources for study personnel • Monitor trial progress and address any issues that arise during the study, employing data-driven approaches to identify and resolve challenges promptly

Qualifications: • Established and experienced support individual contributor; this role is a progression within the level from a Clin Ops Specialist • Broad knowledge of operational systems and practices typically gained through extensive experience and/or education Certifications: • Relevant certifications in clinical operations or related field Necessary Skills: • Strong organizational and communication skills Ability to work under supervision and follow established protocols • Attention to detail and ability to handle routine tasks with some deviation from standard practice • Ability to collaborate effectively with cross-functional teams

For more details, please refer to the company website.