Senior Statistical Programmer

Senior Statistical Programmer (Mexico & Argentina - Hybrid) 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. Job Responsibilities Must be located in Mexico or Argentina - open to working 2 days per week in Mexico City or Buenos Aires Office. Use SAS or other software to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specifications. Work to ensure that outputs meet quality standards and project requirements. Perform validation programming and work with other Programmers, Biostatisticians, and other project team members to resolve discrepancies or any findings. Keep project team members informed of programming progress and issues requiring their attention. Follow applicable SOPs, WIs, and relevant regulatory guidelines (e.g. ICH). Maintain well‑organized, complete, and up‑to‑date project documentation, testing, and verification/quality control documents and programs ensuring inspection readiness. Manage scheduling and time constraints across multiple projects at a time, set goals based on priorities from management, and adapt to timeline or priority changes by reorganizing daily workload. Develop specifications for datasets and outputs of any complexity according to statistical and sponsor requirements. Anticipate and address potential programming issues, reflect forethought, establish the basis for efficient programming and accurately define all variables to be accepted by peer review and sponsor/requestor with little rework. Prepare in advance for internal meetings, contribute ideas, and demonstrate respect for opinions of others. Conduct effective internal meetings (appropriate in format, frequency and attendance). Distribute relevant information in advance. Ensure minutes are promptly and accurately distributed. Follow action items through to completion, and maintain order and focus of meetings, working toward consensus. Display willingness to work with others and assist with projects and initiatives as necessary to meet the needs of the business. Negotiate and establish accurate time estimates for completion of study programming activities with internal team members and statistical programming management, and complete project programming activities within timeframe allotted. Act as the lead statistical programmer. Direct the programming activities of other programming personnel and monitor progress on programming deliverables. Review project documentation such as Statistical Analysis Plan, mock shells, programming specifications, annotated CRFs, and SAS database design. Provide feedback to the appropriate project team members which reflects forethought and reduces inefficiencies in programming activities. Participate in sponsor meetings, kickoff meetings, and bid defense meetings as statistical programming representative, as required by sponsor. Contribute to the mentoring of programming personnel through developing training courses, presenting training materials, reviewing work, and providing feedback or guiding new associates in process. Transfer deliverables. Perform other work‑related duties as assigned. Minimal travel may be required. Qualifications Undergraduate degree, preferably in a scientific or statistical discipline; in lieu of degree, an equivalent combination of education and demonstrated programming experience. Extensive programming experience in SAS or other required software, preferably in a clinical trial environment. Excellent written and verbal communication skills. Ability to read, write, speak and understand English. 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 for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. 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. Company Overview Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever‑changing environment. About Syneos Health Learn more about Syneos Health. Syneos Health® (Nasdaq:SYNH) 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. Together we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. We support a diverse, equitable and inclusive culture. #J-18808-Ljbffr