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Engaged Employer

eClinical Solutions

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2.9

based on 29 Reviews

3 eClinical Solutions Clinical Database Programmer Jobs

Clinical Database Programmer

eClinical Solutions, LLC

2.9

based on 29 Reviews

1-4 years

Bangalore / Bengaluru

1 vacancy

Clinical Database Programmer

eClinical Solutions

posted 1mon ago

Job Role Insights

Fixed timing

Key skills for the job

Data Analysis Informatica PLSQL Microstrategy Datastage QlikView

+ 4 more

Job Description

OVERVIEW

The Clinical Programmer is responsible for developing and maintaining clinical trial programming, ensuring data integrity, and supporting data analysis for clinical studies. The role involves working closely with biostatisticians, clinical data managers, clients and other stakeholders to ensure that all programming tasks are executed accurately and efficiently across all Biometrics Services projects. The Clinical Programmer is accountable for quality, timely and efficient delivery of project programming tasks and quality information management.

KEY TASKS & RESPONSIBILITIES

Read and understand clinical study protocols to better understand the programming needs for a specific trial
Develop and build basic components of clinical databases, including forms and structure, data dictionaries and unit dictionaries
Program a range of simple to complex validations to support validation of the clinical data
Collaborate with cross-functional team members (i.e. Data Managers, Biostatisticians, Coders, etc) and clients to review the business requirements and translate them into database objects and visualizations
Design, develop, test, and deploy highly efficient SQL code and data mapping code according to specifications
Develop and support rigorous QC processes to ensure quality of data deliverables.
Develop ETL code in support of analytic software applications and related analysis projects
Build any analytics reports and visualizations using tools like JReview, Qlik
Provide diagnostic support and fix defects as needed
Ensure compliance with eClinical Solutions/industry quality standards, regulations, guidelines, and procedures
Other duties as assigned

CANDIDATE S PROFILE

Education & Experience

Bachelor s degree and/or equivalent work experience preferred
5+ years in Pharmaceutical/Biotechnology industry or equivalent preferred
Familiarity with EDC Systems: Rave, InForm, or Veeva preferred; previous experience designing eCRFs and edit checks
Knowledge of clinical trial data is a plus - CDISC ODM, SDTM, or ADAM standards
Experience developing back end, database/warehouse architecture, design and development preferred
Knowledge of variety of data platforms including SQL Server, DB2, Teradata, (Cloud based DB a plus)

Professional Skills

Detail oriented, ability to multitask with strong prioritization, planning and organization skills
Excellent knowledge of English; verbal and written communication skills
Proficiency in clinical protocol interpretation and application
Excellent team player
Good understanding of technical challenges and capability to analyze requirement and technical problems
Excited to learn new tools and product modules and adapt to changing technology and requirements

Technical Skills

Proficiency in Microsoft Office 365 Suite including Excel, Word, and Outlook
Experience with requirements gathering, design and specification development of eCRFs, edit checks, and understanding of database structures and programming languages
Knowledge of ICH/GCP guidelines, 21 CFR Part 11, clinical trial methodology, software development lifecycle activities and industry standards (CDASH, SDTM) preferred
Familiarity and/or proficiency with database platforms
Preferred experience in object-oriented programming languages and concepts (i.e. SQL, T-SQL, PL/SQL, C#)
Familiarity with Data Reporting Tools: QlikSense, QlikView, Spotfire, Tableau, JReview, Business Objects, Cognos, MicroStrategy, IBM DataStage, Informatica, Spark or related

Employment Type: Full Time, Permanent

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