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.
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.
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.
Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
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 our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
- We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.
Job responsibilities
- Serve as a lead programmer to design and specify the overall approach to a project’s programming tasks.
- Write project-specific programming code to produce summary data tables and analysis, as specified in the statistical analysis plan.
- Generate draft and final sets of summary data tables and analyses as part of clinical study reports and ISS/ISE documents for regulatory submission.
- Develop programming standards.
- Develop utility SAS macros for use in project programs.
- Develop programming technologies to increase efficiencies in clinical study reporting.
- Validate SAS macros and derived data sets developed by other programmers.
- Coordinate and oversee activities of programming teams, as required for selected projects.
Minimum Requirements
· Bachelor’s Degree in Computer Science, statistics or related area.
· 3+ Years of experience in SDTM Programming.
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