MDR Business Analyst
Full Time
No Travel Required
Remote
Depends on Experience


Siro Clinpharm Pvt Ltd
Fitment
Dice Job Match Score™
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Job Details
Skills
- MDR
- Metadata Repositories
- CDISC
- SDTM
- ADAM
- CDASH
- CT
- Data Models
- APIs
- SQL
- Jira
- Confluence
- Figma
- Visio
Summary
Role- MDR Business Analyst
Experience: 10–15 years
Location: USA, (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 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: 9000791
- Posted 2 days ago
Company Info
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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