Instagram
youtube
Facebook

Clinical Programmer Ii (Dm Sas)

5-7 years
Not Disclosed
10 Dec. 5, 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

The Clinical Programmer II (DM SAS) role at Syneos Health focuses on utilizing SAS and related programming tools to support clinical trial data management and analysis. Below is a summary of the position's responsibilities and qualifications:


Key Responsibilities:

  • Data Programming:

    • Use Advanced SAS programming and macros to develop and maintain clinical data programs from scratch.
    • Apply SQL knowledge to support data extraction, transformation, and reporting needs.
    • Develop and validate SAS programs supporting annotated CRFs, database creation, coding configurations, and edit checks.
    • Generate custom listings, reports, and exports in alignment with study requirements.
  • Project Management:

    • Serve as the lead programmer for up to 8 concurrent clinical studies, coordinating activities with the project team.
    • Proactively manage resources and alert management about delivery or scope changes.
    • Participate in Quick Start Camps (QSCs) to support study initiation and planning.
  • Documentation & Compliance:

    • Ensure all programming deliverables are documented according to company and regulatory standards.
    • Attend sponsor audits and assist with in-progress audits to ensure quality and compliance.
  • Leadership & Collaboration:

    • Provide guidance, training, and mentorship to team members based on expertise in SAS and DM processes.
    • Collaborate with sponsors, internal stakeholders, and cross-functional teams to clarify specifications and meet project objectives.
  • Quality & Continuous Improvement:

    • Review core deliverables for accuracy and ensure alignment with project timelines.
    • Stay updated on industry trends and best practices through training, literature, and professional events.

Qualifications:

  • Education:

    • Bachelor’s degree preferred or equivalent related education and experience.
  • Experience:

    • Clinical Programmer II: 2.9 to 5 years of hands-on experience with Advanced SAS in a data management domain.
    • Senior Clinical Programmer I: 5 to 7 years of relevant experience.
    • Strong experience with SAS macros and developing programs from scratch.
    • Working knowledge of SQL is preferred.
  • Technical Skills:

    • Proficiency in SAS programming and familiarity with additional programming languages like PL/SQL, C#, or VB.
    • Proficient in Microsoft Office Suite (Word, Excel, PowerPoint).
  • Soft Skills:

    • Excellent communication and interpersonal skills for dealing with sponsors and cross-functional teams.
    • Ability to manage multiple priorities in a dynamic environment.
    • Experience working in a matrix-structured environment is preferred.
  • Travel: Ability to travel up to 25% as needed.


Preferred Skills:

  • Background in the data management (DM) domain, particularly within clinical trials.
  • Proven ability to manage study budgets and assess scope of work changes.
  • Experience with sponsor interaction and managing client expectations effectively.

This role offers the chance to leverage SAS programming expertise while contributing to clinical trials in a global organization committed to accelerating life-changing therapies.