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    Clinical Programmer Ii (Veeva/Inform/Rave)

    Syneos Health
    2-6 years
    Not Disclosed
    India
    10 Dec. 1, 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 (Veeva/Inform/Rave) position at Syneos Health is focused on using development tools such as Oracle RDC, Medidata, Rave, and SAS to support clinical programming in clinical trials. This position is ideal for those with experience in eCRF design, programming edit checks, and database management using platforms like InForm, Rave, and Veeva. Here’s an overview:

    Position Overview

    Location: Home-Based, India-Asia Pacific
    Updated: November 22, 2024
    Job ID: 24006203

    As a Clinical Programmer II, you will be responsible for designing, writing, validating, and maintaining clinical programming software, supporting various tools and platforms. You will collaborate with project teams and clients to ensure quality and timely project deliverables in the clinical research environment.

    Key Responsibilities

    1. Clinical Programming Development:

      • Use tools like Oracle RDC, Medidata, Rave, and SAS to design, write, and validate software according to project specifications.
      • Develop and maintain documentation such as CRF specifications, database setup, and edit check procedures.

    2. Project Leadership:

      • Coordinate and lead programming activities for clinical trials, attending project meetings and ensuring milestones are met.
      • Provide constructive feedback, proactively alerting project management of any issues that may impact timelines, scope, or budget.

    3. Quality Control:

      • Ensure deliverables meet accuracy and quality standards, reviewing study-level deliverables and supporting audits.

    4. Mentorship and Training:

      • Provide leadership and guidance to other team members, sharing your expertise in clinical programming to help improve team performance.

    5. Resource and Budget Management:

      • Monitor and manage project resources, flagging any changes or resourcing needs to management.

    Qualifications

    • Education: Bachelor’s degree preferred, or equivalent related experience.
    • Experience:
      • 2 to 6 years of experience in clinical programming with a focus on InForm, Rave, or Veeva.
      • Strong experience in designing eCRFs, programming edit checks in EDC systems, and using InForm or Central Designer.
    • Skills:
      • Strong communication skills to interact with sponsors and internal teams at all levels.
      • Ability to manage multiple priorities and work effectively in a matrix environment.
      • Proficiency in Microsoft Office Suite and familiarity with programming languages like PL/SQL, SAS, C#, or VB is preferred.
      • Ability to travel as necessary (up to 25%).

    Why Syneos Health?

    • Culture:
      Syneos Health promotes a Total Self culture, encouraging authenticity and fostering career development in a supportive environment.

    • Benefits:
      Includes health benefits, 401(k) match, employee stock purchase plan, and flexible paid time off (PTO).

    Application Information

    If you have a strong background in clinical programming and experience with InForm, Rave, and Veeva, and want to contribute to clinical trial success, Syneos Health invites you to apply. Alternatively, you can join their Talent Network to stay updated on future opportunities.

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