01 / SERVICE FRAMEWORK
Study feasibility & site strategy
Evaluate protocol fit, patient population, institutional readiness and the assumptions behind a site strategy.
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SERVICES
Clinical planning.
Connected site operations.
Explore eight planning frameworks for the decisions, people and workflows behind clinical study execution.
02 / SERVICE FRAMEWORK
Site activation & coordination
Connect start-up requirements, documentation and milestones through clearly assigned responsibilities.
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03 / SERVICE FRAMEWORK
Participant support planning
Plan practical support around visit demands, communication needs and barriers to participation.
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Adaptive study resourcing
Define the roles, qualifications, supervision and handovers required by the study scope.
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05 / SERVICE FRAMEWORK
Clinical data workflow planning
Map records, system access, data queries and responsibilities before study workflows are established.
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06 / SERVICE FRAMEWORK
Quality & governance planning
Set decision rights, issue escalation, documentation standards and an agreed oversight cadence.
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Clinical supply coordination planning
Identify equipment and consumable requirements, supply dependencies and work requiring qualified vendors.
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Regulatory coordination planning
Clarify submission pathways, local requirements and responsibilities requiring authorized professional advice.
Explore this serviceTHINKROMAN ECOSYSTEM
Technology within the ThinkRoman ecosystem
Spence
A ThinkRoman platform connecting clinical trial and site operations with the records, responsibilities and evidence behind them.
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Your protocol.
Our starting point.
Tell us what your study needs. Together, we can define the right scope, responsibilities and next steps.