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Principal Scientific Data Curator
Medasource
- New York, New York, United States
- New York, New York, United States
Über
Senior Scientific Data Curator
to support enterprise-level curation, metadata strategy, and data governance across preclinical, translational, and clinical R&D. This is a
fully remote, year-long contract role
supporting high-impact analytics, regulatory readiness, and cross-program data integration in a fast-paced, regulated pharmaceutical environment.
This role sits at the intersection of science, data platforms, and product leadership and partners closely with clinical, data science, engineering, and IT teams across the organization.
Key Responsibilities
Provide expert curation and annotation of complex scientific and clinical data assets, including:
Anatomical and tissue data
Assay and experimental metadata
Biomarker and multi-omics datasets
Clinical trial and clinical operations data
Real‑World Data (RWD)
Medical imaging data
FDA and regulatory feedback artifacts
Perform
SDTM-aligned curation
to support regulatory compliance and submission readiness.
Curate oncology clinical trial laboratory, biomarker, and imaging datasets for downstream analytics and reporting.
Support microbiome and metagenomic sequencing studies through metadata sourcing, annotation, and quality review.
Design, implement, and maintain enterprise metadata frameworks, controlled vocabularies, and cataloging standards.
Apply disease, literature, and ontology‑based annotations to enable cross‑study and cross‑program data integration.
Harmonize metadata across preclinical, translational, and clinical domains.
Define, monitor, and continuously improve data quality control (QC) metrics and validation processes.
Support data modeling efforts aligned with platform architecture and analytics use cases.
Platform Enablement & Automation
Partner closely with data platform engineering teams to enable scalable ingestion and curation workflows.
Collaborate with software developers to design and implement automation for metadata population and validation within the enterprise data catalog.
Curate and integrate data from internal and external sources, including:
cBioPortal
GTEx
Open Targets
TCGA
UniProt
Leverage enterprise engineering tools and workflows, including HTML and Git/GitHub.
Data Governance & Compliance
Contribute to enterprise data governance initiatives, including stewardship models, data standards, and data lifecycle management.
Ensure curated data assets meet expectations for auditability, traceability, and regulatory inspection readiness.Promote and operationalize
FAIR data principles
(Findable, Accessible, Interoperable, Reusable) across the data platform.
Cross‑Functional Leadership & Product Ownership
Provide technical project leadership across clinical, translational science, data science, and IT stakeholders.
Act as an internal
product owner
for data catalog and curation capabilities by:
Gathering and prioritizing user requirements
Tracking feature requests and defects
Coordinating testing and validation with end users
Partner with platform teams and external vendors to align roadmap priorities and delivery timelines.
Apply Agile methodologies to manage deliverables in a regulated pharmaceutical environment.
Scientific & Therapeutic Area Expertise
Apply scientific domain expertise across multiple therapeutic areas, including:
Oncology
Cardiovascular diseases
Gastrointestinal diseases
Immune and infectious diseases
Metabolic diseases
Neurologic diseases and neuroscience
Support preclinical (in vivo rodent) and wet‑lab data curation with a strong focus on translational relevance.
Qualifications & Skills
PhD in a life sciences discipline with strong grounding in biology and experimental data interpretation.
Experience supporting enterprise data platforms within pharmaceutical or biotech R&D environments.
Deep understanding of clinical trial data standards, metadata management, and regulatory considerations.
Proven ability to bridge scientific, technical, and product-focused teams.
Excellent written and verbal communication skills for both scientific and non‑scientific audiences.
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Sprachkenntnisse
- English
Hinweis für Nutzer
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