Job Description

Description Sr Statistical Programmer Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our customers achieve their objectives.. Undergraduate Degree, preferably in a scientific or statistical discipline . Min 5 years in programming in SAS preferably in a clinical trial environment. . Should have good proficiency in end-to-end programming including SDTM, ADaM, TFLs . Good to have experience as Lead . Excellent written and verbal communication skills. . Ability to read, write, speak, and understand English. 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. Clinical Pharmacology and Bioanalysis Syneos Health offers a breadth of services across the entire product development lifecycle and our Clinical Pharmacology and Bioanalysis teams provide seamless multidisciplinary solutions, using a collaborative approach to support our customers\' early development needs with Clinical, Bioanalytical, and Biometrics/Pharmacometrics support. As a Statistical Programmer in Clinical Pharmacology & Bioanalysis, you will have an opportunity to work on end-to-end programming for promising therapeutics and across phases supporting development of new chemical entities (NCEs). Job responsibilities . Uses SAS or other software to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specifications. . Works to ensure that outputs meet quality standards and project requirements. . Performs validation programming and works with other Statistical Programmers, Biostatisticians, and other project team members to resolve discrepancies or any findings. . Keeps project team members informed of programming progress and issues requiring their attention. . Follows applicable SOPs, WIs, and relevant regulatory guidelines (e.g. ICH). . Maintains well organized, complete, and up-to-date project documentation, and verification/quality control documents and programs ensuring inspection readiness. . Manages scheduling and time constraints across multiple projects, sets goals based on priorities from management, and adapts to timeline or priority changes by reorganizing daily workload. . May develop specifications for datasets and outputs according to statistical and Sponsor requirements. Anticipates and addresses potential programming issues, reflects forethought, establishes the basis for efficient programming, accurately defines all variables to be accepted by peer review and sponsor/requestor with little rework. . Prepares in advance for internal meetings, contributes ideas, and demonstrates respect for opinions of others. . Displays willingness to work with others and assist with projects and initiatives as necessary to meet the needs of the business. . Completes project programming activities within timeframe allotted by Lead Statistical Programmer and/or management. . May act as the Lead Statistical Programmer, directs the programming activities of other programming personnel and monitors progress on programming deliverables. . Assists with the transfer of deliverables. . Performs other work-related duties as assigned. . Minimal travel may be required. Qualifications What we\'re looking for . Undergraduate Degree, preferably in a scientific or statistical discipline . Min 5 years in programming in SAS preferably in a clinical trial environment. . Should have good proficiency in end-to-end programming including SDTM, ADaM, TFLs . Good to have experience as Lead . Excellent written and verbal communication skills. . Ability to read, write, speak, and understand English. Get to know Syneos Health 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. Learn more about . 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 . 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.

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