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Rave Custom Function Programmer

IQVIA
2-3 years
INR 8-14 LPA
Kolkata, India
10 June 16, 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, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, CPT, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, HCPCS Level II, ICD-10-CM, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICD-10-PCS, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing

Key Responsibilities

Clinical Database Development & Maintenance

  • Plan and coordinate database design, development, implementation, maintenance, and user support for clinical systems.

  • Build new database modules and maintain global libraries for clinical trials.

  • Modify existing modules in collaboration with Data Management teams.

  • Manage and maintain global library objects across multiple clinical projects.

Data Standards & Library Management

  • Implement clinical data standards and data models.

  • Develop and maintain Global Library (GLIB) objects for clinical data collection.

  • Ensure consistency and reusability of standard clinical database components.

  • Maintain Global Library Copy Groups for standard page reuse across studies.

Cross-Functional Collaboration

  • Work closely with:

    • Data Managers

    • Study Start-Up Teams

    • Database Developers

    • Data Standards Governance Teams

    • Metadata Teams

  • Understand clinical data collection and submission requirements.

Validation & Programming

  • Develop, test, document, and maintain:

    • CDMS validations

    • Derivations

    • Procedures

  • Utilize programming languages and tools such as:

    • SQL

    • PL/SQL

    • C#

    • VB Script

    • SAS

Issue Resolution & Process Improvement

  • Identify and resolve issues impacting global library delivery.

  • Escalate critical issues to leadership when required.

  • Recommend best practices for:

    • Data modeling standards

    • Global Library conventions

    • CDMS implementation guidelines

Documentation & Compliance

  • Create metadata specifications for:

    • Data collection

    • Data transformation

    • CDISC SDTM submissions

  • Contribute to SOP reviews and business guidance documentation.


Required Skills & Knowledge

Clinical Data Standards

  • Basic understanding of CDISC Standards

  • Knowledge of SDTM implementation

Clinical Database Systems

  • Strong experience with Medidata Rave (Rave Certification preferred)

  • Global Library maintenance and procedure building

  • Custom function programming

Technical Skills

  • Clinical Data Management Systems (CDMS)

  • Relational Databases

  • eCRF Development

  • Validation and Derivation Programming

  • Scripting Language Experience (Preferred)

Soft Skills

  • Attention to Detail

  • Quality Focus

  • Time Management

  • Customer Focus

  • Strong Communication Skills

  • Ability to explain technical concepts to non-technical stakeholders


Preferred Candidate Profile

Must Have

  • 2+ years Clinical Database Programming experience

  • Medidata Rave expertise

  • Global Library management experience

  • Clinical trial database setup experience

  • Knowledge of CDISC standards

Good to Have

  • SQL / PL-SQL programming

  • SAS programming

  • C# or VB Script experience

  • Validation and derivation programming experience