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Sr Statistical Programmer (Adam / Tfl's+ Sdtm)

1+ years
Not Disclosed
10 Nov. 29, 2024
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Statistical Programmer

Company: Syneos Health
Location: [Location not specified]


About Syneos Health

Syneos Health is a fully integrated biopharmaceutical solutions organization, dedicated to accelerating customer success by translating clinical, medical affairs, and commercial insights into outcomes that address the realities of modern markets. With a global presence and a commitment to innovation, Syneos Health works with 29,000 employees across 110 countries to improve the delivery of therapies that change lives.

"Work Here Matters Everywhere"


Why Syneos Health?

At Syneos Health, we invest in the development of our people through career growth, peer recognition, and ongoing training. Our Total Self culture fosters diversity, inclusion, and authenticity, creating a supportive environment where everyone feels they belong.


Role Overview

As a Senior Statistical Programmer, you will be responsible for leading the development and validation of statistical programs, managing project timelines, ensuring the quality and accuracy of data, and mentoring junior programmers. This role involves extensive use of SAS and other software tools to generate statistical outputs such as tables, listings, graphs, and datasets in compliance with study requirements.


Key Responsibilities

  • Statistical Programming:

    • Develop custom SAS programs or use other required software to generate statistical outputs (summary tables, data listings, graphs, and derived datasets) as specified in the statistical analysis plan (SAP).

    • Ensure outputs meet quality standards and align with project requirements.

    • Perform validation programming, troubleshooting discrepancies, and collaborating with biostatisticians and other team members.

  • Project Management & Communication:

    • Provide regular updates on programming progress and issues to the project team.

    • Manage multiple projects simultaneously, setting goals and adjusting timelines as necessary to meet changing priorities.

    • Lead internal meetings, ensuring clear communication, accurate distribution of minutes, and effective resolution of action items.

  • Quality Control & Documentation:

    • Maintain organized, complete, and up-to-date project documentation, ensuring inspection readiness.

    • Review project documentation such as the Statistical Analysis Plan, mock shells, and annotated CRFs to identify potential inefficiencies and reduce programming issues.

  • Team Leadership & Mentorship:

    • Act as the lead statistical programmer, overseeing the programming activities of other programmers.

    • Mentor junior team members, developing training courses, providing feedback, and guiding new associates.

    • Participate in sponsor meetings, kickoff meetings, and bid defense meetings as the statistical programming representative.

  • Collaboration & Contributions:

    • Contribute to the preparation of programming specifications, addressing potential issues early to ensure efficient programming.

    • Assist with the transfer of deliverables and contribute to process improvements to streamline workflows.


Qualifications

Education & Experience:

  • Undergraduate degree in a scientific or statistical discipline, or equivalent combination of education and experience.

  • Extensive experience programming in SAS (or other relevant software), particularly in a clinical trial environment.

  • Strong knowledge of statistical methodologies and experience with clinical trial datasets.

Skills & Competencies:

  • Excellent written and verbal communication skills.

  • Ability to read, write, and understand English fluently.

  • Experience with programming specifications and statistical analysis plans (SAPs).

  • Strong organizational skills, capable of managing multiple tasks and deadlines.

Additional Requirements:

  • Ability to work independently and collaboratively within a team.

  • Minimal travel may be required for the role.


Why Work with Us?

  • Career Development: Opportunities for growth within an innovative and dynamic environment.

  • Collaborative Culture: Work with passionate professionals in a company dedicated to improving health outcomes.

  • Inclusive Workplace: Syneos Health is committed to diversity, equity, and inclusion, providing a place where everyone feels valued.

  • Comprehensive Benefits: Competitive salary and benefits package, including health and retirement options.


Apply Now to be part of Syneos Health, a leader in accelerating the delivery of therapies that change lives worldwide.


Syneos Health encourages applicants from all backgrounds to apply, especially those with transferable skills. Join our Talent Network to stay connected to future opportunities.