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. 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.
Senior Statistical Programmer
Location
India
Posted
173 days ago
Salary
0
Seniority
Senior
Job Description
Senior Statistical Programmer
Syneos Health
• Uses SAS or other software to develop custom programming code to generate summary tables, data listings, graphs and derived datasets • Works to ensure that outputs meet quality standards and project requirements • Performs validation programming and collaborates with other team members to resolve discrepancies • Maintains organized project documentation and quality control documents • Manages scheduling across multiple projects and adapts to changes in priorities • Develops specifications for datasets and outputs based on requirements • Prepares for and conducts effective internal meetings • Acts as lead statistical programmer and directs programming activities of others
Job Requirements
- Undergraduate degree, preferably in a scientific or statistical discipline
- 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
Benefits
- Career development and progression
- Supportive and engaged line management
- Technical and therapeutic area training
- Peer recognition and total rewards program
- Total Self culture promoting authenticity
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