Clinical Support Specialist | Ideal Opportunity for Regulatory, Study Start-Up & Site Activation Specialists | Argentina Hybrid

Clinical Support Specialist | Ideal Opportunity for Regulatory, Study Start-Up & Site Activation Specialists | Argentina Hybrid 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.   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.   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.   Discover what your 25,000 future colleagues already know:   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 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.  • 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.  Job Responsibilities • Responsible for providing operational and administrative support to one or more clinical functions. • Responsibilities may include but are not limited to: • Provide administrative support by coordinating documentation and communications, including maintaining and managing shared mailboxes, organizing project files, tracking action items, and ensuring timely follow-up with cross-functional stakeholders. • Enter, maintain and reconcile information in agreed project and clinical tracking systems. • Timeline and milestone tracking. • Perform document management activities including document creation, compilation, formatting, version control, and quality control (QC). • Translation of documents using approved vendors/systems • Use AI-enabled tools, dashboards, and automated reports to provide logistical, organizational, and analytical support • Support Trial Master File (TMF) filing and related document process activities within scope, ensuring inspection-ready documentation. • Responsible for providing quality deliverables. Follow project requirements and applicable country rules, with oversight at the project level from functional leads. • Review and comply with applicable Standard Operating Procedures (SOPs) and Work Instructions (WIs), ensure training compliance, and maintain accurate timesheet reporting. • Monitor workload/scope, budgeted effort, and project hours; escalate discrepancies in a timely manner • Maintains overall awareness in the field of clinical research by completing all necessary and assigned training

Qualifications: • Associate’s degree or equivalent combination of education, training and experience. • Minimum 1 year clinical operations experience • Demonstrated understanding of clinical operations • Utilize problem-solving techniques effectively • Strong documentation and communication skills (written and spoken English) as well as a team[1]oriented approach. • Proficiency in Microsoft Office Suite (Outlook, Word, Excel, PowerPoint, Publisher) and ability to embrace new technologies and