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Rave Custom Function Programmer

Iqvia
IQVIA
1 years
Not Disclosed
Thane, India
10 Feb. 20, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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: Rave Custom Function Programmer

Location: Thane, India
Job Type: Full-Time
Work Mode: Hybrid
Job ID: R1499688

Company Overview
IQVIA is a global leader in clinical research services, healthcare intelligence, and commercial insights for the life sciences industry. The organization supports pharmaceutical, biotechnology, and medical device companies in accelerating clinical development and improving patient outcomes worldwide.

Job Summary
IQVIA is seeking a skilled Rave Custom Function Programmer to support clinical database programming and custom function development within Medidata Rave EDC environments. The role involves programming edit checks and custom functions using C#.Net, interpreting data validation specifications, and ensuring compliance with clinical and regulatory standards.

This opportunity is ideal for professionals with strong technical expertise in C#.Net programming and hands-on experience in Electronic Data Capture (EDC) systems within the clinical research domain.

Key Responsibilities

  • Read, interpret, and program Medidata Rave edit checks and custom functions (C# programming) based on Data Validation Specifications (DVS).

  • Ensure programming aligns with client requirements and clinical study protocols.

  • Demonstrate strong working knowledge of Electronic Data Capture (EDC) systems.

  • Apply Good Clinical Practice (GCP) guidelines and clinical domain standards in all programming activities.

  • Implement post-production changes and perform impact assessments.

  • Provide technical suggestions and solutions to operational and database-related challenges.

  • Collaborate with corporate teams and Clinical Data Management (CDM) teams to align timelines, deliverables, and responsibilities.

  • Develop internal tools and automation solutions for quality metrics using Excel, Visual Studio, or other platforms.

  • Work independently with minimal supervision while meeting project milestones.

  • Follow structured coding and software development best practices.

Required Technical Skills

  • Strong expertise in C#.Net programming.

  • Experience in Medidata Rave Custom Function and Edit Check programming.

  • Knowledge of EDC systems and clinical trial data workflows.

  • Understanding of Good Clinical Practice (GCP) and regulatory standards.

  • Familiarity with database administration principles.

  • Proficiency in tool development using Excel, Visual Studio, or related platforms.

  • Strong analytical, troubleshooting, and problem-solving skills.

Education Requirements

  • Bachelor’s Degree in Computer Science, Information Technology, Life Sciences, or a related field (or equivalent professional experience).

Experience Required

  • Minimum 1 year of experience in database administration, EDC programming, or clinical database programming.

  • Experience working in the clinical research or healthcare domain is preferred.

Core Competencies

  • Clinical database programming

  • Medidata Rave custom function development

  • C#.Net application development

  • Edit check programming and validation

  • Cross-functional collaboration in clinical trials

Why Join IQVIA
IQVIA offers exposure to global clinical research projects, innovative technologies, and collaborative cross-functional teams. Professionals joining IQVIA gain the opportunity to contribute to impactful healthcare solutions while building expertise in clinical data programming and regulatory-compliant development environments.

IQVIA maintains a strict zero-tolerance policy for candidate fraud and requires complete accuracy and integrity throughout the recruitment process.