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Sr Statistical Programmer(Sdtm, Adam &Tlf)

0-2 years
Not Disclosed
10 April 7, 2025
Job Description
Job Type: Remote 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

 

Job Title:

Senior Statistical Programmer

Company:

Syneos Health®


Company Overview:

Syneos Health® is a fully integrated biopharmaceutical solutions provider, combining clinical development, medical affairs, and commercial capabilities. With 29,000 employees across 110 countries, it focuses on accelerating the delivery of therapies by bringing together customer insight and innovation to improve outcomes.


Why Syneos Health:

  • Strong focus on employee development and career progression

  • Supportive and engaged leadership

  • Training in technical skills and therapeutic areas

  • Peer recognition and rewards programs

  • Inclusive and authentic Total Self culture

  • Collaborative and innovative global work environment


Job Responsibilities:

  • Develops custom programming code using SAS or similar software to generate summary tables, listings, graphs, and derived datasets per the SAP and specifications

  • Ensures deliverables meet quality standards and project timelines

  • Performs validation programming and resolves data discrepancies with project team

  • Follows SOPs, WIs, and regulatory guidelines such as ICH

  • Maintains organized, complete, and up-to-date documentation and quality control materials

  • Manages scheduling and priorities across multiple projects

  • Develops specifications for datasets/outputs, proactively identifies programming issues, and proposes efficient solutions

  • Contributes ideas and preparation to internal meetings; documents and follows up on action items

  • Collaborates with others on business initiatives and projects

  • Estimates and negotiates timelines for programming activities and delivers on time

  • Leads statistical programming efforts and monitors work of junior programmers

  • Reviews project documents like SAPs, annotated CRFs, mock shells, specifications, and provides constructive feedback

  • Participates in sponsor meetings, kickoff meetings, and bid defenses as needed

  • Mentors team members by developing and delivering training, reviewing work, and guiding processes

  • Transfers deliverables as required

  • Performs additional work-related duties as assigned

  • Minimal travel may be required


Qualifications:

  • Undergraduate degree in scientific/statistical discipline preferred (or equivalent education/experience)

  • Extensive SAS programming experience in a clinical trial setting

  • Excellent verbal and written communication skills

  • Fluent in English (reading, writing, speaking, understanding)


Additional Information:

  • Duties may vary depending on business needs

  • Equivalent experience/education may be accepted

  • This is not a binding employment contract

  • The company is compliant with the Americans with Disabilities Act and EU Equality Directive, providing accommodations as needed