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Full‑Service Consulting

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Transform how you deliver clinical trials

Our full‑service consulting practice helps biopharma organisations streamline their eClinical operations—from supply chain and logistics to demand planning, technology integration and governance.  

We conduct rigorous assessments, benchmark you against industry leaders and deliver actionable roadmaps for improvement.

Why BC Consulting?

Our consultants have deep experience across clinical supply, eClinical systems, quality management and clinical operations.  We bring an objective, data‑driven perspective that delivers actionable insights for process optimisation, cost reduction and operational agility.  Our recommendations are tailored to your portfolio and growth objectives, ensuring scalability and compliance.

Our Approach

We use a structured, data‑driven methodology to diagnose issues, benchmark against best practices and design future‑state models:

We interview stakeholders, map processes and collect performance data across your supply chain and adjacent eClinical functions.  

This baseline reveals pain points such as long study start‑up timelines, forecasting inefficiencies and disconnected workflows.

We benchmark your organisation against top pharmaceutical companies, develop a SWOT analysis and prioritise improvement opportunities.  

Areas we examine include organisational design, system integrations, regulatory impact, and more.

We define an optimised target operating model with process enhancements, technology recommendations and governance improvements.  

The final deliverables include future‑state process maps, a phased implementation plan and change‑management guidance.

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What We Address

Organisational design & efficiency – Evaluate structure and role alignment; improve interfaces with functions like clinical operations and data management.

Systems & technology – Assess and optimise eClinical systems; recommend digital tools for visibility, automation and control.

Forecasting & demand planning – Benchmark forecasting methodologies; enhance supply‑demand alignment to minimise waste and accelerate study start‑up.

Operations & logistics – Analyse clinical supply processes and vendor oversight; optimise study support ratios and logistical workflows.

Comparator & ancillary sourcing – Develop sourcing models and vendor strategies to balance cost, speed and supply continuity.

Regulatory & compliance – Strengthen governance frameworks, documentation and escalation pathways to meet evolving regulatory requirements.

Talent & training – Review resourcing strategies; design career paths; provide training and change‑management support to ensure adoption.

Cross‑functional integration – Improve collaboration between supply chain, clinical operations, IT and finance; facilitate informed decision‑making and risk mitigation.

 

 

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Engagement Options

If you are ready to optimise your clinical programs, systems, or operational teams, we are ready to help.  

Get a free and non-salsey consultation now to better understand if we are a fit for you and your company. 

 

Contact Us

Schedule a consultation to learn how our full‑service consulting can accelerate study start‑up, reduce costs and future‑proof your organisation.