Senior Clinical Programmer

2 days ago


Hyderabad, Telangana, India Syneos Health Full time ₹ 6,00,000 - ₹ 18,00,000 per year

Roles & Responsibility

  • Utilizes primary development tools including Medidata, Rave, Oracle OC/RDC, Oracle Inform, and/or SAS, and other supporting tools to design, write, validate, and maintain software to meet specifications in a timely and productive manner following standard development procedures.
  • • Generates and maintains all required documentation, including the development of specifications, programs, and validation efforts in support of annotated Case Report Forms (CRFs), database creation, coding configuration, edit check procedures, import setup and processing, export setup and processing, listings, and custom reports..
  • • Serves on project teams to coordinate and lead development activities for clinical programming projects. Attends meetings, participates in discussions, uses an analytical approach to problem solving, focuses on deliverables, and provides constructive feedback. Keeps those responsible for project management informed of any issues that might impact project target dates, scope, or budget and escalates potential problems effectively and in a timely manner. Balances multiple task assignments and communicates needs to supervisor to obtain needed resources.
  • • Provides technology support to the clinical programming staff, Project Analysts, Data Managers, etc., who design, write, validate, and maintain software to meet specifications in a timely and productive manner following standard development procedures. This includes support of the development of specifications, coding, and validation efforts in support of annotated CRFs, database creation, coding setup, edit-check procedures, import setup and processing, export setup and processing, listings, and custom reports
  • • Provides application administration and technical support as the subject matter expert on core business packages including but not limited to: Oracle Inform, MDSOL Rave, Oracle RDC, -, SAS, and supplemental packages such as migration mentor/review, reporting tools, custom functions.
  • • Ensures high quality deliverables by providing senior review of study level/program level/multi study core deliveries for accuracy. Attends sponsor audits and assists with inprogress audits.
  • • Reviews and provide input on study budgets and monitors scope of work to actual work, alerting management of potential change orders; manages and executes the change order to completion. Provides input and supporting details for change orders.
  • • Monitors applications for workflow alerts, system errors, and performance issues. Provides second tier help desk support, as needed.
  • • Performs system integration activities, application updates, and user acceptance testing.
  • • Provides leadership, training, guidance, and support to other department members based upon expertise in specific skill sets. Collaborates with clients, peers, lead programmers, project teams, and/or requestors to clarify and finalize specifications; uses expanded technical skills to meet evolving project needs.
  • • Assists in project meetings and actively contributes and participates in departmental review meetings.
  • • Attends Quick Start Camps (QSCs) as the lead Clinical Programmer role for assigned studies.
  • • Leads clinical programming activities on three (3) to ten (10) concurrent studies depending upon scope, similarity, program, and resourcing requirements.
  • • Manages project resources, proactively alerting management of delivery and resourcing needs.
  • • Possesses and maintains a broad overall knowledge in the field of clinical programming and clinical data management by reading related literature, self-training, attending training classes, attending professional meetings, etc.

Preferred Qualification

  • Bachelors degree preferred, or equivalent combination of related education and experience.
  • 5+ years of total experience, ability to Lead the Clinical Study Design and Specification documentation to support efficient Database Build activities.
  • Strong experience in Custom Function Programming (Min. 4 years of experience on Custom Function Programming).
  • Minimum 3 years of Experience on Migration (Post DB Changes) activities, preferably able to perform Impact Analysis.
  • Medidata Rave and iMedidata experience (Edit and form designing), Edit Check Programming and review, Understanding and Programming Dynamic edits, Experience in Global Libraries, Generating eCRF PDF Reports.
  • The ability to deal effectively with sponsors and internal customers at all levels.
  • Excellent communication and interpersonal skills, both written and spoken, with an ability to inform.
  • Demonstrated experience in managing multiple priorities in a highly dynamic environment
  • Experience working in a matrix-structured environment is preferred
  • Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), email, and Voicemail
  • Experience with programming languages, such as PL/SQL, SAS, C#, or VB preferred.
  • Ability to travel as necessary (up to 25%)

Interested candidates kindly share there updated resume


  • clinical programmer

    3 days ago


    Hyderabad, Telangana, India Clinotica Full time ₹ 9,00,000 - ₹ 12,00,000 per year

    Job Description:JOB SUMMARYThis position functions as a member of the Biostatistics and Statistical Programming project team supporting the Lead Statistical Programmer in the development of programs to support the conduct statistical analysis and reporting of projects. A Statistical Programmer I creates, tests and maintains programs for clinical studies,...


  • Hyderabad, Telangana, India Statistics & Data Corporation (SDC) Full time ₹ 15,00,000 - ₹ 20,00,000 per year

    Principal Clinical Programmer (RAVE EDC)Statistics & Data Corporation (SDC), a specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC providing a technology enabled service offering to provide clients with both...


  • Hyderabad, Telangana, India Perceptive Inc. Full time ₹ 20,00,000 - ₹ 25,00,000 per year

    As a Senior Clinical Data Programmer, your core responsibility is to understand complex business requirements and identify strategic opportunities to drive efficiency and value through data. Leverage advanced programming languages, scripts, and software tools to perform sophisticated data extraction, transformation, and validation, ensuring the highest...


  • Hyderabad, Telangana, India Perceptive Full time ₹ 6,00,000 - ₹ 12,00,000 per year

    We're on a mission to change the future ofclinical research. At Perceptive, we help thebiopharmaceutical industry bring medicaltreatments to the market, faster.Our mission is to change the worldbut to do this, we need people like you.Apart from job satisfaction, we can offer you:HEALTH:Medical plan for you and your dependents.Personal Accident InsuranceLife...


  • Hyderabad, Telangana, India Veramed Full time ₹ 1,20,000 - ₹ 1,80,000 per year

    Position :Principal SAS ProgrammerLocation :Bangalore/Hyderabad/IndiaJob SummaryVeramed is seeking a hands-on Principal SAS Programmer with a strong work ethic and attention to detail to join our statistical and programming team. The ideal candidate will provide high-quality programming support for a variety of clinical trials, working on datasets, TFLs, and...


  • Hyderabad, Telangana, India Amgen Technology Private Limited Full time ₹ 8,00,000 - ₹ 24,00,000 per year

    Manager, CSAR - SAS Clinical Data Reporting and Spotfire Programmer Career CategoryEngineering Job Description Join Amgen's Mission of Serving Patients At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we've...


  • Hyderabad, Telangana, India Medpace Full time ₹ 9,00,000 - ₹ 12,00,000 per year

    Medpace, a rapidly growing global Clinical Research Organization (CRO), is excited to announce that we're looking for experienced full-time, Hyderabad-based Clinical Database Programmer to join us as we prepare to launch of our newest office inHyderabad, India.This is more than just a job. It's an opportunity to be part of something from the very beginning....


  • Hyderabad, Telangana, India Capgemini Full time ₹ 12,00,000 - ₹ 18,00,000 per year

    Your RoleWe are seeking an experienced and collaborative Senior Statistician I to provide advanced statistical expertise and leadership in support of clinical research studies. This role involves working closely with Biostatisticians, Statistical Programmers, Clinical Data Managers, and sponsor teams to ensure the accuracy, reliability, and regulatory...


  • Hyderabad, Telangana, India NextByt Innovations Full time ₹ 15,00,000 - ₹ 25,00,000 per year

    Senior (6+ yrs): Hands-on experience in R programming with expertise in migrating SAS codes to R. Skilled in developing interactive R Shiny applications for clinical trial reporting and visualization. Strong knowledge of statistical programming, data validation, and Pharma domain workflows.Junior (3+ yrs): Proficient in R programming with exposure to R Shiny...


  • Hyderabad, Telangana, India Amgen Inc Full time ₹ 15,00,000 - ₹ 25,00,000 per year

    Manager, CSAR - SAS Edit Check Programmer*What you will do* The Manager, CSAR - SAS Edit Check Programmer will report to the Sr. Manager, Clinical System and Analytical reporting and will be focused on supporting SAS Edit check programming activities. The Manager, CSAR - SAS Edit Check Programmer will create and implement edit checks, adhering to Amgen...