Life Sciences & Biotech Consulting

Connect the work behind your next life sciences milestone

GrandView helps life sciences teams connect the plans, data, workflows, and decisions behind clinical and product milestones. We work across Pharmaceuticals & Biopharma, Biotechnology, and Medical Devices & Diagnostics, improving the work around established IBM and specialist systems without making platform replacement the starting point.

Isometric life sciences program hub connected with clinical work, laboratory evidence, planning, manufacturing and governed AI
Three operating realities
Pharmaceuticals & Biopharma Biotechnology Medical Devices & Diagnostics
IBM ecosystem expertise

Business context, architecture, and delivery in one team

GrandView connects the business question to the systems and delivery work required to answer it. Our experience in planning, analytics, data, integration, and AI governance helps us see where a program problem is really a model, data, workflow, or ownership problem.

20 years average consulting experience across our team

Principal-led delivery

Senior specialists stay involved from diagnosis through implementation.

One accountable partner

Planning, data, integration, analytics, and platform expertise stay connected.

A faster path to evidence

Reusable patterns and working models show dependencies before implementation.

Enterprise technology, applied to the way life sciences teams work

Select a partnership to see how it supports planning, data, workflow, and platform improvements around established systems.

IBM Gold Business Partner

Connect planning, data, and AI to a defined business decision

We connect IBM analytics, data, integration, automation, and AI capabilities to a specific life sciences workflow instead of beginning with a technology program.

Planning AnalyticsCognosIntegrationwatsonx

The operational problems life sciences teams cannot solve in one system

Life sciences work crosses teams, partners, documents, models, and specialist applications. A decision may begin with a clinical or product event and move through planning, evidence, review, and approval before anyone can act on it.

Plan

The plan falls out of date when the program changes

Enrollment, site activation, protocol, vendor, or product timing can move during a reporting cycle. The financial view often catches up after teams have already started working from the new reality.

Evidence

The decision waits while people rebuild its context

Study data, contracts, invoices, quality records, and prior assumptions may each answer part of the question. Review starts after someone finds and reconciles them.

Partners

Important work happens outside the organization

CROs, sites, laboratories, manufacturers, and specialist vendors create data and costs the sponsor still has to understand. Their updates arrive on different schedules and in different formats.

Business impact

The first part of the decision becomes reconciliation

Finance, R&D, Clinical Operations, and leadership may work from different timelines, cost assumptions, or versions of the program before they can agree which view is current.

Exception

Standard reports can hide the change that matters most

A delayed site, supplier change, missing document, or unusual quality event may have more business impact than the normal cases around it. These changes often remain in email or manual trackers.

AI control

AI can prepare the work, but people still own the decision

Teams need to know which sources an AI service used, what it was asked to do, how its output was checked, and who approved the next action.

One industry.Three operating realities.

The underlying constraint may be shared. Its business impact depends on the product, company stage, and work being performed.

Operating challenge Pharmaceuticals & BiopharmaPortfolio and commercial scale BiotechnologyClinical-stage biotech Medical Devices & DiagnosticsProduct and quality lifecycle
Program work Development, manufacturing, launch, and commercial plans affect one another across a portfolio. A small number of programs depend on sites, CROs, laboratories, specialist vendors, and the timing of the next milestone. Product, software, quality, manufacturing, and post-market work continue across the same lifecycle.
Business measures Portfolio value, R&D spend, capacity, launch timing, product performance, and revenue outlook. Milestone timing, study spend, accruals, cash burn, runway, and the next financing need. Development spend, resource use, unit cost, quality events, service performance, and product revenue.
Decision data Clinical, portfolio, finance, manufacturing, supply, and commercial views across planning cycles. Enrollment, site, vendor, milestone, contract, invoice, resource, and cash assumptions. Product, design, quality, manufacturing, complaint, service, and post-market information.
Partner ecosystem Research partners, CROs, manufacturers, distributors, and commercial partners contribute to the operating view. Sites, CROs, laboratories, consultants, and vendors create much of the evidence, activity, and cost. Suppliers, contract manufacturers, laboratories, service partners, and clinical sites affect product and quality work.
Improvement priority Connect portfolio and financial planning across established systems and reporting environments. Connect program assumptions to cost, cash, runway, and management scenarios as the timeline changes. Connect product and quality information while keeping specialist systems responsible for their records.

Better life sciences decisions require a shared view

One program change can cross several executive mandates. The improvement has to make sense to the people responsible for delivery, financial performance, architecture, data, AI, quality, and regulatory control.

R&D & Clinical Operations

Can we see how a change in enrollment, site timing, or resources affects the program plan?

Milestones · sites · vendors · delivery

CFO & Finance

Can we explain runway and the next financing need using assumptions the program teams recognize?

Spend · accruals · cash · scenarios

A life sciences program decision connected to clinical operations, finance, data and AI, quality and regulatory review
Shared life sciences decisionOne milestone · one operating context
CIO, Data & AI

Can teams reuse data and AI without losing source context, access control, or ownership?

Architecture · access · lineage · model lifecycle

Quality & Regulatory

Can we reconstruct the evidence, review, and approval behind the result?

Evidence · review · change history

Start with the business problem. Improve only what solves it.

We diagnose before we prescribe. The engagement begins with the business outcome and the way work happens today, not with a predetermined platform.

01

Define the outcome

Choose one process or decision and agree how improvement will be measured: forecast cycle, manual adjustments, wait time, rework, missing information, or time to an approved answer.

Output · agreed baseline and decision
02

See the complete workflow

Reconstruct how representative work moves across teams, partners, systems, spreadsheets, and documents. Map assumptions, owners, exceptions, review points, and controls.

Output · current-state evidence map
03

Improve a practical scope

Select a bounded flow such as a trial forecast, portfolio review, cash runway model, quality event, supply decision, or defined use of AI.

Output · controlled intervention design
04

Prove the operating result

Test the flow with real roles, representative data, and the exceptions that usually cause trouble. Keep required review and approval with the people responsible for the decision.

Output · measured pilot evidence
05

Scale from evidence

Use the result to decide what should expand, what should stay unchanged, and where the next investment will improve the outcome.

Output · next-step roadmap

Technology that improves how life sciences work gets done

GrandView combines the capabilities required by the workflow instead of forcing the entire problem into one product category. The architecture depends on the organization's existing systems, process, data, and controls.

GrandView helps Finance and program teams build or improve models for trial budgets, cash forecasts, portfolio choices, workforce, and management reporting. For clinical-stage biotech, this connects enrollment, site timing, vendor estimates, and program milestones to cash burn, runway, and funding scenarios.

Technology layer
  • IBM Planning Analytics
  • TM1
  • IBM Cognos Analytics
Explore Planning Analytics
Connected planning models feeding a governed analytics environment and management dashboard

Let's identify where GrandView can make the clearest difference

Bring us one plan that keeps falling behind the program, one decision that begins with conflicting assumptions, or one data or AI constraint holding back useful work. We will help you determine whether the issue sits in the model, workflow, data, integration, platform, or operating ownership.

Schedule a Life Sciences Diagnostic
Rusty Pennington, CFO and Partner at GrandView
Rusty Pennington CFO & Partner, GrandView Business planning and technology advisory
IBM Business Partner IBM ecosystem expertise for life sciences planning, data, analytics, automation, AI governance, and platform modernization