Project Associate

Project Associate (Ideal for people with experience with Global studies) English Advance - Hybrid position Buenos Aires ARG 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 make Syneos Health easier to work with and 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 about changing lives. Job Responsibilities Drive the planning and execution of elements of clinical trials in partnership with the Project Lead. Ensure projects adhere to strict timelines and are delivered within budget. Coordinate internal resources and third parties/vendors for efficient execution of projects. Conduct ongoing analysis of project performance to drive the successful completion of short- and long-term goals. Maintain and distribute study-specific financial reports and contribute to study’s financial health. Document project scope and objectives, involving all relevant stakeholders. Lead communication between project team members, ensuring all parties are informed of project status and changes. Document and escale project risks and issues and drive timely follow-through and completion. Maintain systems and project management tools and methodologies. Drive quality assurance activities, including preparation for audits and internal review, prepare documentation, and follow through to resolution on actionable issues. Job Summary The Project Associate will drive and support overall project management activities to ensure successful execution of clinical trials, which may range from single service studies to full scope or multiple protocol and/or global projects. This role requires coordination of project tasks, maintaining documentation, communicating with stakeholders, and maintaining timelines and budgets. A Project Associate may be allocated to function at the Sr. Project Associate (Sr. PA) level within a large project team or on a small project. Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the job description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences are expressed in brief terms. All language contained herein fully complies with the obligations imposed by the legislation of each country in which it operates, including the EU Equality Directive, in relation to recruitment and employment. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Seniority Level Entry level Employment Type Full-time Job Function Management and Manufacturing #J-18808-Ljbffr