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Sr Clinical Programmer (Dm Sas)

5 years
Not Disclosed
10 Sept. 10, 2025
Job Description
Job Type: Remote Education: B.Sc/ M.Sc/ M.Pharm/ B.Pharm/ Life Sciences 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 Clinical Programmer (DM SAS)


About Syneos Health®

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We combine clinical, medical affairs, and commercial insights to deliver meaningful outcomes for patients.

  • Global Presence: 29,000 employees in 110 countries

  • Our Culture: Total Self – where everyone feels they belong

  • Our Mission: Simplify, innovate, and accelerate therapy delivery to change lives

  • Our Commitment: Career growth, supportive leadership, training, and recognition

WORK HERE MATTERS EVERYWHERE


Why Join Us

  • Career development and progression opportunities

  • Supportive, engaged leadership team

  • Technical and therapeutic training programs

  • Peer recognition and total rewards programs

  • Inclusive and diverse culture that values authenticity


Key Responsibilities

  • Design, develop, validate, and maintain clinical programming deliverables using tools such as Medidata Rave, Oracle Inform, Oracle OC/RDC, SAS.

  • Develop and maintain documentation (specifications, CRFs, edit checks, coding setup, exports, listings, custom reports).

  • Lead programming activities for multiple concurrent studies (3–10 depending on scope).

  • Support clinical programming staff and cross-functional teams with technical guidance.

  • Provide SME-level support for core applications (Rave, Oracle RDC, Inform, SAS).

  • Conduct system integration, application updates, and user acceptance testing.

  • Perform senior-level review of programming deliverables for accuracy and compliance.

  • Participate in audits, sponsor reviews, and departmental meetings.

  • Monitor study budgets, manage change orders, and ensure alignment with project scope.

  • Provide training, mentoring, and leadership to peers and junior programmers.

  • Collaborate with clients, project teams, and requestors to clarify and finalize specifications.

  • Maintain knowledge of industry trends in clinical programming and data management.


Qualifications

  • Education: Bachelor’s degree preferred (or equivalent experience).

  • Experience: Minimum 5+ years in clinical programming.

  • Technical Skills:

    • Proficiency in SAS (Base/Advanced certification preferred).

    • Experience with listings programming, macro development, SAS mapping.

    • Knowledge of CDISC standards, external/vendor data mapping, and DIA preferred.

    • Familiarity with PL/SQL, C#, or VB is a plus.

  • Therapeutic Experience: Any therapeutic area acceptable.

  • Other Skills:

    • Strong communication and interpersonal skills.

    • Ability to manage multiple priorities in a dynamic, matrix environment.

    • Proficiency in MS Office (Word, Excel, PowerPoint).

    • Willingness to travel up to 25%.


About Syneos Health – By the Numbers

  • Partnered on 94% of FDA-approved novel drugs (past 5 years)

  • Supported 95% of EMA-authorized products

  • Conducted 200+ studies across 73,000 sites with 675,000+ trial patients


Additional Information

  • Responsibilities may evolve at the company’s discretion.

  • Equivalent experience may be considered in place of listed qualifications.

  • Syneos Health complies with ADA and provides reasonable accommodations when needed.

  • Committed to diversity, equity, and inclusion in every aspect of hiring.


👉 Learn more: www.syneoshealth.com
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