Principal Statistical Programmer Sponsor Dedicated - US hiring

Syneos Health; United States; On-site; USD 81,000 - 145,000; Full time

Benefits offered by this job

Company car or car allowance

Health benefits (Medical, Dental, Visn

401k match

Employee Stock Purchase Plan

Paid time off

Job summary

Syneos Health is seeking a Principal Statistical Programmer for US-based hiring. The role leads programming for compound studies, maintaining timelines and standards while mentoring junior programmers. You will review CDISC validation outputs and support submissions under supervision.

The ideal candidate has 8+ years SAS/Base/Macro/GRAPH experience in biopharma or CROs, solid data management with CDISC, and strong leadership and organizational skills.

Qualifications

• BA/BS degree required; MS in statistics or computer sciences is desired.
• Minimum 8 years of programming experience using SAS/Base/Macro/GRAPH in biopharma or CROs.
• Data management experience with CDISC standards is highly desirable.
• Strong SAS programming skills and attention to detail are essential.
• Knowledge of regulatory guidelines including electronic submission standards.
• Strong organizational, time management, communication and leadership skills.

Responsibilities

• Function as a Lead programmer for a compound or group of studies.
• Maintain the overall timeline for studies and programming standards.
• Review standard macros and datasets; allocate resources for groups of studies.
• Mentor junior programmers on Incyte systems and standards.
• Assist in study set-up and identify similar studies.
• Ensure validation reports are clean and properly documented.
• Act as programming lead for submissions under supervision of management.
• Provide expert recommendations to complex problems and mentor junior staff.

Skills

SAS programming

Leadership

Time management

Communication

Project coordination

Education

BA/BS degree (MS in statistics or computer sciences desired)

Tools

CDISC

Job description

Principal Statistical Programmer Sponsor Dedicated - US hiring

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.

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 deliver - for one another, our customers, and, most importantly, for those in need.

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 building an inclusive culture - where you can authentically be yourself. Central to this is our purpose - Driven to Deliver - which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone's life.
• We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.

Job Responsibilities

Essential Functions of the Job (Key responsibilities)

• Function as a Lead programmer for a compound or a group of studies performing the following functions:
• Maintain the overall timeline for his/her studies.
• Maintain the programming standards for his/her studies.
• Review standard macros used; Review standard datasets used.
• Discuss need for programming resources for their group of studies.
• Mentor/Train junior programmers on Incyte systems and standards as they work on studies within their area.
• Assist junior programmers in new study set-up to help identify similar studies.
• Review Production area after study programming is complete to make sure datasets, programs, and outputs are properly stored.
• Check that the validation summary reports are clean of errors and warnings, and show proper documentation of SAS programs.
• Review individual study CDISC validation output.
• Act as a Programming lead for a submission project under supervision of Programming management.
• Serve as a mentor to junior programmers and as an expert to provide recommendations and solutions to complex problems.

Qualifications (Minimal acceptable level of education, work experience, and competency)

• BA/BS degree (MS degree in statistics or computer sciences is desired).
• Minimum 8 years of programming experience using SAS/Base/Macro/GRAPH in the biopharmaceutical and/or CRO industries.
• Data Management experience including CDISC standard is highly desirable.
• Good SAS programming skills and attention to detail are essential.
• Demonstrate knowledge of regulatory guidelines, including electronic submission standards.
• Strong organizational, time management, communication and project coordination and leadership skills.
• Must be able to work well under timeline pressure.
• Must be able to work on multiple tasks while coordinating others at the same time.
• Demonstrate experience serving as a mentor to junior programmers and as an expert to provide recommendations and solutions to complex problems.

At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.

Salary Range:

$80,600.00 - $145,000.00 The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate's qualifications, skills, competencies, and proficiency for the role.

Get to know Syneos Health

Over the past 5 years, we have worked wit