Find a jobRecruiters

Senior Clinical Programmer

Exclusive opportunity

Onsite

Senior Clinical Programmer

SDC Clinical

Senior Clinical Programmer

Skills

Google Cloud PlatformSQL QueriesC#.NETDatabase AdministrationCompliance

9 days ago

Share this opportunity

Share this opportunity to other talents of your network:
✓ Offer them a visibility boost with clients.
✓ Help your contacts find their next job.

Important information


Contract type:

Permanent

Location:

Hyderabad, Telangana, India

Work mode:

Onsite

Published on:

17 October 2026

What they need


Job highlights

  • Utilize copies of like database elements from library structures or other similar studies during builds. Batch load external data from vendors (e.g.,central lab data).
  • Commensurate experience with clinical database programming and database administration will be considered as an alternative to a degree

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 provides a technology-enabled service offering to provide clients with both clinical services expertise, as well as the technology they need to be successful in their clinical trials.

Job Summary

Works as part of a project team to design and implement clinical database applications in support of clinical research and biostatistics analysis. Works with clinical data managers and biostatisticians to develop database build specifications and gain acceptance through user testing. Develops data entry screens and programs, and data quality edit checks to comply with related specifications. Accomplishes database structure testing. Processes database programming change requests. Documents all work fully according to FDA regulations and guidances, and company SOPs. Actively promotes standards for the development and acquisition of systems. Communicates with the end-users. Mentors/trains junior level clinical programmers.

Responsibilities

  • Assist in developing, validating, and maintaining clinical databases for clinical trials using a variety of validated software applications
  • Provide complete and accurate documentation of study databases consistent with company standard operating procedures (SOPs), study protocols and related data management plans
  • Build and validate data entry screens (paper and/or electronic data capture (EDC))
  • Implement and test data quality checks in accordance with the study data validation manual
  • Assist in developing and maintaining global library of clinical database forms, edit checks, and other regularly used programs and routines
  • Utilize copies of like database elements from library structures or other similar studies during builds
  • Batch load external data from vendors (e.g., central lab data)
  • Participate in internal and external team meetings, as necessary
  • Assist in management of user access to clinical databases
  • Assist in managing and updating medical coding dictionaries, including but not limited to MedDRA and WHODrug
  • Participate in writing departmental documentation (e.g., training documents, process guidances)
  • Participate in other clinical programming and data management activities, as required
  • Mentor junior level clinical programmers
  • Adhere to all aspects of the Statistics & Data Corporation's quality system
  • Comply with Statistics & Data Corporation's data integrity & business ethics requirements
  • Perform other related duties incidental to the work described herein
  • Adherence to all essential systems and processes that are required at SDC to maintain compliance to business and regulatory requirements

Requirements

  • At least six years of experience assuming lead database programming responsibilities on projects, with a minimum of 3 years in a clinical environment
  • Excellent understanding of relational database structures
  • Fast, accurate programming skills using assorted application software
  • PL/SQL, SQL, and XML programming skills
  • FDA regulations and guidances (e.g., 21 CFR Part 11, ICH/GCP)
  • Knowledge of installation and/or validation of clinical data management system (CDMS) applications in a clinical research environment
  • C#, C++, .NET, Visual Basic or other object-oriented language, and/or SAS programming knowledge/experience not required, but desirable
  • Medidata Rave and iMedNet EDC knowledge/experience not required, but desirable
  • Reporting application development (e.g. JReview, Business Objects, Spotfire) knowledge/experience not required, but desirable

Education or Equivalent Experience

  • Bachelor's degree in computer science or other quantitative or scientific discipline with 6+ years of experience in database programming and demonstrated working knowledge of scientific principles.
  • Commensurate experience with clinical database programming and database administration will be considered as an alternative to a degree.

Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

Other offers great for you!

These companies are also looking for great profiles

Anderson RH

Développeur IA agentique Sénior - Banque de financement

Freelance

Paris, France

Hybrid

Skills

PythonAgentic AIMulti-agent systemsModel Context Protocol (MCP)LangGraphCrewAIDéveloppeur IA agentique (MCP / agents / skills) — Tests & qualité en BFI

19 hours ago

Quick apply

Achil

Manager / Senior Manager Audit Financier H/F – Lille (59)

Permanent contract

Lille, France

Onsite

3 hours ago

Quick apply

Achil

Manager / Senior Manager Audit Financier H/F – Bordeaux (33)

Permanent contract

Bordeaux, France

Onsite

3 hours ago

Quick apply

The best place to find your next move

© 2026. All Rights Reserved.

Talents

Find a job

Create a profile

Solutions and tools