Advanced Research Assistance for Established Scholars
From Study Design to Data-Driven Insights
ProData Analytics partners with established scholars to design robust studies, run advanced analyses, and translate results into publishable, high-impact insights, all with speed, rigor, and reproducibility.
Advanced Research Assistance for Established Scholars From Study Design to Data-Driven Insights
ProData Analytics partners with established scholars to design robust studies, run advanced analyses, and translate results into publishable, high-impact insights, all with speed, rigor, and reproducibility.
Who This Is For
Tenured or research-intensive faculty leading labs, centers, or multi-investigator projects.
PIs on complex grants (R01/U01/center grants; PCORI; foundation awards).
Scholars with high data complexity (longitudinal, hierarchical, multi-omics, EHR, or linkage data).
Authors targeting elite journals seeking precise, defensible analyses and narratives.
What We Deliver (at a glance)
Study design & protocol architecture (power, endpoints, biases, analytic plans).
Advanced statistical modeling (mixed effects, causal inference, survival, Bayesian, ML).
Data strategy (EHR/registry curation, missing data, harmonization).
Publication-ready artifacts (tables/figures, methods text, reviewer-response strategy).
Grant-ready packages (aims alignment, statistical sections, mock results).
Reproducible workflows (versioned code, pipelines, and documentation).
Core Services (with icons)
Study Design & Protocol Development (icons: fa-bullseye, lucide: target)
Hypothesis refinement; primary/secondary endpoints; estimands.
Sample size & power (parallel, cluster, stepped-wedge, adaptive).
Randomization schemes; stratification; covariate-adaptive methods.
Bias & confounding mitigation plans; sensitivity frameworks.
Full SAP (Statistical Analysis Plan) synced to CONSORT/STROBE/PRISMA as appropriate.
Data Architecture & Curation (fa-database, lucide: database)
EHR/registry extraction maps; CDM harmonization (OMOP/PCORnet).
Data dictionaries; codebooks; derivation logic; version control.
Missing data strategy (multiple imputation, IPCW, sensitivity).
Quality checks (range, logic, outlier forensics, duplicate resolution).
Advanced Analytics (fa-chart-line, lucide: line-chart)
Causal inference: IPTW/AIPW, MSMs, g-methods, propensity score matching/weighting.
Longitudinal & multilevel: mixed effects, GEE, random slopes, growth curves.
Time-to-event: Cox, competing risks (Fine–Gray), recurrent events, joint models.
Bayesian analysis: hierarchical models, priors elicitation, posterior predictive checks.
Machine learning: regularization (LASSO/elastic-net), tree ensembles, survival ML, SHAP.
Meta-analysis: pairwise & network meta-analysis, heterogeneity & publication bias.
Diagnostic rigor: assumptions, residuals, robustness, falsification endpoints.
Result Interpretation & Decision Support (fa-compass, lucide: compass)
Effect translation into clinical/public-health relevance.
Subgroup & interaction narratives (pre-specification vs. exploration).
What-if scenarios and policy/clinical implications.
Graphical explanations for stakeholders and reviewers.
Publication & Reviewer Strategy (fa-newspaper, lucide: file-text)
Methods & results drafting aligned with journal scope & reporting standards.
High-impact tables/figures: CONSORT, flow diagrams, forest plots, Kaplan–Meier, DAGs.
Response to reviewers: point-by-point strategy, added analyses, clarity edits.
Grant Support for Advanced Projects (fa-file-signature, lucide: file-signature)
Aims alignment with a coherent program of research.
Statistical & data sections; feasibility mockups; pilot analyses.
Milestones, timeline/Gantt, data-sharing & rigor/reproducibility language.
Letters on analytic capacity and data governance.
Reproducible Science & Compliance (fa-code-branch, lucide: workflow)
Versioned repos; workflow automation (R/Quarto, Python, targets/drake, Snakemake).
Reproducible reports with parameterized notebooks.
IRB, HIPAA/PHI safeguards; de-identification pipelines; audit trails.
Our Collaboration Model
- Scoping & Feasibility (no-pressure consult): We clarify aims, data realities, and target journals/grants; propose a fit-for-purpose plan.
- Analysis Blueprint: You receive a concise Analysis Blueprint: data plan, models, robustness checks, sample outputs, and delivery schedule.
- Execution & Check-ins: Work proceeds in sprints with milestone reviews. You see interim outputs and can request pivots.
- Delivery Package : Clean outputs, publication-ready figures/tables. Annotated code and reproducible notebooks. Methods, language blocks, and limitations/assumptions notes.
- Submission & Reviewer Support: Rapid add-on analyses, supplemental figures, and response-to-reviewer drafting.
Signature Deliverables (examples)
Power & design dossier (PDF + editable text)
Statistical Analysis Plan (SAP) aligned to your protocol
Validated dataset + data dictionary + derivation specs
Analysis notebooks (R/Python) + executable environment files
Publication-ready figures (vector: SVG/EPS; bitmap: PNG/TIFF @300–600 dpi)
Methods/results language tailored to target journal
Reviewer response matrix with tracked revisions
Engagement Options
Expert Consult Blocks (fa-user-tie, lucide: user-cog)
- Reserved hours for senior-level consultation, design decisions, and analytic arbitration.
Project Sprint (fa-rocket, lucide: rocket)
- 2–6 week sprint for a specific manuscript, aim, or grant section with defined milestones.
Lab Partnership (fa-flask, lucide: beaker)
- Quarterly partnership for labs/centers—pipeline monitoring, junior-faculty mentoring, standing code reviews.
Quality & Rigor You Can Count On
Transparent assumptions and pre-specified sensitivity analyses.
Reproducibility by default (versioned code, deterministic seeds, environment capture).
Plain-language translation for clinical/administrative audiences.
Security: encrypted transfer, least-privilege access, PHI safeguards.
FAQs (quick hits)
Can you work with secure institutional environments?
Yes—VPN, VDI, VPC, and on-prem compute; we comply with institutional policies and IRB constraints.
Do you ghostwrite manuscripts?
We prepare methods/results text and figures; authorship follows ICMJE/discipline norms you specify.
Will you run my team’s code?
Yes. We can audit, optimize, or containerize existing pipelines with explicit change logs.
Callouts You Can Use on the Page
“Complex designs, clean decisions.”
“From raw EHR to reviewer-ready figures.”
“Rigor you can cite—and reproduce.”
CTA: Let’s architect your next high-impact study.
Request a Consultation »