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Sr Clinical Programmer (Veeva)

0-2 years
Not Disclosed
10 May 5, 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 Clinical Programmer (Veeva)

Job Location: India - Asia Pacific - Home-Based


Company Overview

Syneos Health is a global leader in biopharmaceutical solutions, offering integrated services across clinical development, medical affairs, and commercial strategy to accelerate the delivery of therapies. The company emphasizes customer success, innovation, and operational efficiency, working in over 110 countries.


Role Summary

As a Senior Clinical Programmer, you will be responsible for designing, writing, validating, and maintaining clinical software using primary development tools like Medidata, Oracle Inform, SAS, and others. You will also lead and support clinical programming activities, ensuring high-quality deliverables and managing multiple clinical studies.


Key Responsibilities

  • Utilize tools such as Medidata, Oracle OC/RDC, Oracle Inform, and SAS to design, write, validate, and maintain software according to specifications.

  • Develop and maintain documentation, including specifications, programs, and validation efforts, for clinical programming projects.

  • Lead development activities for clinical programming projects, participating in meetings and providing constructive feedback.

  • Provide technology support to clinical programming staff, Data Managers, and other team members, assisting with the development of specifications and validation efforts.

  • Provide application administration and technical support as the subject matter expert on core business packages (Oracle Inform, MDSOL Rave, SAS, etc.).

  • Ensure high-quality deliverables by reviewing study-level/program-level deliverables for accuracy.

  • Attend sponsor audits and assist with in-progress audits.

  • Monitor system performance, handle workflow alerts, and provide second-tier help desk support.

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

  • Lead and train other department members based on expertise in specific skill sets.

  • Manage project resources and alert management to any resourcing or delivery needs.

  • Lead clinical programming activities on multiple concurrent studies.

  • Stay up to date with clinical programming and clinical data management literature and best practices.


Qualifications

Required

  • Education: Bachelor’s degree or equivalent experience in a related field.

  • Experience:

    • Experience managing multiple priorities in a dynamic environment.

    • Experience with clinical programming tools like Medidata, Oracle Inform, SAS, etc.

    • Strong communication and interpersonal skills, both written and verbal.

    • Ability to work in a matrix-structured environment and manage multiple projects.

  • Skills:

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

    • Programming knowledge in languages like PL/SQL, SAS, C#, or VB preferred.

    • Ability to travel as necessary (up to 25%).

Preferred

  • Experience with clinical data management and clinical programming in a regulated environment.


Work Environment

Syneos Health offers a dynamic, diverse, and supportive environment, promoting Total Self culture, career development, and ongoing employee engagement. The company emphasizes a team-oriented approach and works to create a workplace where everyone feels a sense of belonging.


How to Apply

Interested candidates can apply through the Syneos Health career portal.