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Business Analyst – Clinical Metadata Repository (MDR)

Remote • Posted 2 days ago • Updated 2 days ago

Full Time

No Travel Required

Remote

Depends on Experience

Siro Clinpharm Pvt Ltd

Fitment

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Job Details

Skills

Clinical trial processes & data lifecycle
Clinical Metadata Repository (MDR)
CDISC standards: SDTM
ADaM
CDASH
Controlled Terminology (CT)
Regulatory compliance: FDA & EMA
Data models
metadata schemas & mappings
MDR platforms/metadata services
Functional understanding of APIs & technical designs
Jira
Confluence
SQL
Strong communication & stakeholder management
Analytical problem-solving
Cross-functional collaboration
Attention to detail & quality-focused approach
CDISC
Clinical Trials
Regulatory Compliance

Clinical trial processes & data lifecycle
Clinical Metadata Repository (MDR)
CDISC standards: SDTM
ADaM
CDASH
Controlled Terminology (CT)
Regulatory compliance: FDA & EMA
Data models
metadata schemas & mappings
MDR platforms/metadata services
Functional understanding of APIs & technical designs
Jira
Confluence
SQL
Strong communication & stakeholder management
Analytical problem-solving
Cross-functional collaboration
Attention to detail & quality-focused approach
CDISC
Clinical Trials
Regulatory Compliance

Summary

Job title : Business Analyst – Clinical Metadata Repository (MDR)

Location : Remote

Required Skills & Competencies

Domain & Functional

Strong understanding of clinical trial processes and data lifecycle
Hands‑on experience with:

Clinical Metadata Repositories (MDR)
CDISC standards (SDTM, ADaM, CDASH, CT)

Knowledge of regulatory submissions and compliance (FDA, EMA)

Technical & Analytical

Experience working with data models, metadata schemas, and mappings
Familiarity with MDR‑related platforms or technologies (e.g., graph DBs, metadata services)
Ability to read and collaborate on technical designs and APIs (functional perspective)

Tools

Requirements & documentation: Jira, Confluence, Word, Excel
Design & validation: Figma, Visio
Data & metadata concepts: SQL (read‑level understanding preferred)

Soft Skills

Excellent communication and stakeholder management skills
Strong analytical and problem‑solving mindset
Ability to work in cross‑functional, global teams
Detail‑oriented with a structured, quality‑first approach

Preferred / Nice to Have

Experience working on enterprise MDR implementations
Exposure to standards automation, up‑versioning, or data reuse initiatives
Prior experience with Pfizer / large pharma MDR or standards programs

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 91163707
Position Id: 9029467
Posted 2 days ago

Company Info

About Siro Clinpharm Pvt Ltd

Founded in 1996 as the SIRO Research Foundation and incorporated in 2000 as SIRO Clinpharm Private Limited, SIRO brings over two decades of exceptional project management expertise to the table. From pioneering proof-of-concept trials to managing complex, multinational studies involving rare diseases, stringent protocols, and accelerated timelines, SIRO has consistently delivered with precision and reliability. Our win-win philosophy drives us to ensure success for every client. Today, SIRO stands as a leading provider of drug development and discovery solutions, offering a diverse and innovative suite of CRO services to global biotech, pharmaceutical, medical device, and academic institutions. To better serve our clients’ evolving needs, we have strategically reorganized into three specialized entities: SIRO Clintech, SIRO Medical Writing, and SIRO Clinpharm, which continues to offer specialized FSP services.

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Pratyush Diwedi

Recruiter @ SpringPoint Technologies

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Remote

•

29d ago

Role OverviewWe are seeking an experienced Business Analyst with expertise in Clinical Metadata Repositories (MDR) and CDISC standards to support enterprise clinical data standards and metadata management initiatives. The ideal candidate will act as a bridge between business stakeholders, clinical standards teams, and technology teams to define, manage, and optimize metadata-driven processes across the clinical trial lifecycle. Key ResponsibilitiesGather, analyze, and document business requireme

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Full-time