Principal Stat Programmer(ADAM & TLF)

Syneos Health, Inc.; Madhapur; On-site; INR 1,200,000 - 2,400,000; Full time

Job summary

Syneos Health in Madhapur, India is seeking an experienced Lead Statistical Programmer to drive programming deliverables across multiple clinical trials. You will lead the statistical programming activities, develop datasets and outputs per SAP and CDISC standards, and mentor junior programmers.

Requires 8+ years in Clinical SAS, strong ADaM/ADaM specs, client-facing experience, and excellent communication. Travel minimal.

Qualifications

• Require 8+ experience in Clinical SAS, Base SAS, Advance SAS, SAS/Macros.
• Strong experience in ADaM programming including ADaM specifications and dataset generation.
• Good to have experience of ISDB-ISS, pooling study.
• Must have experience of client handling, leading studies.
• Good to have experience of both safety & efficacy data.
• Experience in mentoring others in clinical trial process and CDISC Standards.
• Strong communication skills, problem-solving abilities, and ability to work collaboratively in a dynamic environment.

Responsibilities

• Uses SAS to develop programming code for summary tables, data listings, graphs and derived datasets as specified in the SAP.
• Performs validation programming and coordinates with team members to resolve discrepancies.
• Follow SOPs, WIs, and regulatory guidelines (ICH).
• Maintain project documentation, testing and QC for inspection readiness.
• Manage scheduling across multiple projects and adapt to timelines and priorities.
• Develop specifications for datasets/outputs per sponsor requirements and ensure proper variable definitions.
• Lead internal meetings and track action items to completion.

Skills

Clinical SAS

Base SAS

Advanced SAS

SAS Macros

Client handling

Mentoring others

Communication skills

Job description

Updated: Today
Location: Madhapur, TS, India
Job ID: 25110083

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.

Discover what your 25,000 future colleagues already know.

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

• Uses 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. Works to ensure that outputs meet quality standards and project requirements.
• Performs validation programming and works with other 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.
• Follow applicable SOPs, WIs, and relevant regulatory guidelines (e.g. ICH).
• Maintains well organized, complete, and up-to-date project documentation, testing, and verification/quality control documents and programs ensuring inspection readiness.
• Manages scheduling and time constraints across multiple projects at a time, sets goals based on priorities from management, and adapts to timeline or priority changes by reorganizing daily workload.
• Develops specifications for datasets and outputs of any complexity according to statistical or sponsor requirements. Anticipates and addresses potential programming issues, reflects forethought, establishes the basis for efficient programming and accurately defines all variables to be accepted by peer review and sponsor/requestor with little rework.
• Conducts effective internal meetings (appropriate in format, frequency and attendance). Distributes relevant information in advance. Ensures minutes are promptly and accurately distributed. Follows action items through to completion, and maintains order and focus of meetings, working toward consensus.
• Displays willingness to work with others and assist with projects and initiatives as necessary to meet the needs of the business.
• Accountable for on-time delivery across concurrent programming deliverables. Negotiates programming timelines and provides risk mitigation plans for projects or programs, as needed. Proactively informs management of the status of deliverables and significant project or program issues, including planned resolutions.
• Acts as the lead statistical programmer. Directs the programming activities of other programming personnel and monitors progress on programming deliverables.
• Reviews project documentation such as Statistical Analysis Plan, mock shells, programming specifications, annotated CRFs, and SAS database design. Provides feedback to the appropriate project team members which reflects forethought and reduces inefficiencies in programming activities.
• Participates in sponsor meetings, kickoff meetings, and bid defense meetings as statistical programming representative, as required by sponsor.
• Contributes to the mentoring of programming personnel through developing training courses, presenting training materials, reviewing work, and providing feedback or guiding new associates in process.
• Maintains a good working knowledge of clinical drug development, industry standards, and electronic submission requirements; serves as a technical expert resource to other department members for complex programming questions.
• Works cooperatively with other biostatistics and statistical programming personnel to establish standard operation procedures (SOPs), guidelines, policies, and/or procedures.
• Contributes technical expertise to the development of programming tools and macros for standardization and efficiency.
• When serving as a technical subject matter expert for CDISC and other industry and regulatory requirements, provides guidance and training to the Biostatistics group and other departments on the appropriate use of CDISC Standards.
• When serving as a subject matter expert for CDISC and other industry and regulatory requirements, performs compliance reviews of project deliverables for CDISC deliverables including SDTM and ADaM specifications and datasets as well as any regulatory required documents. (i.e. DEFINE.XML)
• When serving as a subject matter expert for CDISC and other industry and regulatory requirements, actively participates in industry standards organizations and provides regular updates to the Biometrics Department on upcoming changes to those standards.
• Transfers deliverables.
• Performs other work-related duties as assigned.
• Minimal travel may be required.

Qualifications

• Require 8+ experience in Clinical SAS, Base SAS, Advance SAS, SAS/Macros.
• Strong experience in ADAM & TLF programming including ADaM specifications, dataset generation.
• Good to have experience of ISDB-ISS, pooling study.
• Must have experience of client handling, leading studies.
• Good to have experience of both safety & efficacy data.
• Experience in mentoring others in clinical trial process and CDISC Standards.
• Strong communication skills, problem-solving abilities, and ability to work collaboratively in a dynamic 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.