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Senior Principal Clinical Programmer

0-2 years
Not Disclosed
10 Oct. 1, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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 Principal Clinical Programmer

Location:

IND – Remote

Job ID:

25101935

Updated:

September 26, 2025

Company:

Syneos Health® – fully integrated biopharmaceutical solutions organization


Job Summary:

The Senior Principal Clinical Programmer leads and oversees clinical programming activities for single studies or large programs of studies. This role manages multiple project timelines and deliverables, mentors less experienced programmers, ensures quality and compliance of outputs, and serves as a subject matter expert in clinical programming, data management, and associated tools (SAS, Python, Veeva, SDTM).


Qualifications / Expectations:

  • Bachelor’s degree required; Master’s preferred, or equivalent education and experience.

  • Ability to engage effectively with sponsors and internal stakeholders at all levels (senior-level stakeholder management).

  • Excellent written and verbal communication skills.

  • Demonstrated experience managing multiple priorities in a dynamic environment (project management skills).

  • Experience in a matrix-structured environment preferred.

  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint), email, and voicemail.

  • Clinical data and programming expertise (SAS, Python).

  • Knowledge of medical or safety review dashboards/listings.

  • SDTM and Veeva data knowledge preferred.

  • Understanding of systems, tools, processes, and technicalities for system/tool migrations.

  • Experience mentoring others in clinical trial processes.

  • English proficiency (read, write, speak, understand).


Key Responsibilities:

Technical & Programming Support

  • Provide technical support and expertise across clinical programming and data management functions.

  • Serve as subject matter expert for core business packages: Veeva, SAS, Python, Spotfire, and other tools.

  • Develop, validate, and maintain software to meet specifications using standard development procedures.

  • Generate and maintain documentation: specifications, coding, validation, CRF annotation, database creation, edit checks, import/export setup, listings, and custom reports.

  • Monitor applications for workflow alerts, errors, and performance issues; troubleshoot defects.

  • Perform system integration activities, application updates, and user acceptance testing.

Project Leadership & Management

  • Lead development activities for clinical programming projects; attend and participate in meetings and discussions.

  • Provide senior review of program-level/multi-study core deliveries for accuracy and quality.

  • Participate in bid defenses, sponsor audits, and in-progress audits.

  • Manage project resources and oversee multiple concurrent studies (5–20 studies depending on scope and resourcing).

  • Review study budgets, monitor project metrics, and manage change orders.

Team Leadership & Mentorship

  • Provide leadership, mentorship, guidance, and support to department members.

  • Assign project work, review workloads, and manage staff development for junior programmers.

  • Resolve conflicts and prioritize tasks at the program level.

Process Improvement & Innovation

  • Update SOPs and work instructions in line with departmental and company processes.

  • Lead development of process improvements, programming tools, and new concepts/technologies to meet emerging needs.

  • Oversee external vendor management, including integrations, implementations, and SLA monitoring.


Skills & Competencies:

  • Advanced clinical programming, project management, and analytical skills.

  • Expertise in SAS, Python, SDTM, Veeva, and associated clinical data tools.

  • Ability to manage multiple projects and programs simultaneously.

  • Strong stakeholder management and communication skills.

  • Knowledge of regulatory and industry standards for clinical data.


Additional Information:

  • Minimal travel may be required.

  • The role may involve supervisory responsibility and oversight for a team of lead clinical programmers within a program.


Company Overview:

Syneos Health® has over 29,000 employees across 110 countries. The company provides clinical development, medical affairs, and commercial solutions, emphasizing patient-centered innovation and accelerating therapy delivery.

Website: www.syneoshealth.com


Diversity & Inclusion:

Syneos Health is committed to building a diverse, inclusive, and authentic workplace. Transferable skills are considered, and reasonable accommodations are provided for employees or applicants with disabilities.


Job Category:

Clinical / Data Management / Statistical & Clinical Programming