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

  1.  Scoping & Feasibility (no-pressure consult): We clarify aims, data realities, and target journals/grants; propose a fit-for-purpose plan.
  2.  Analysis Blueprint:  You receive a concise Analysis Blueprint: data plan, models, robustness checks, sample outputs, and delivery schedule.
  3.  Execution & Check-ins: Work proceeds in sprints with milestone reviews. You see interim outputs and can request pivots.
  4. Delivery Package : Clean outputs, publication-ready figures/tables. Annotated code and reproducible notebooks. Methods, language blocks, and limitations/assumptions notes. 
  5. 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.
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