Services

Medical support, from the development question to the clinical detail.

Five connected areas of support, shaped around your programme, priorities and existing team. Engagements can cover focused advice, defined projects or ongoing medical involvement.

Explore the service areas

01Clinical development strategy and study design 02Medical monitoring and safety oversight 03Medical leadership and sponsor oversight 04Clinical documentation and regulatory support 05Australian trial planning and investigator engagement

How Proxima can help

Specific support, considered in context.

Each service starts with the sponsor’s actual need. The scope is then shaped around development stage, internal capability and the practical value Proxima can add.

Clinical development strategy and study design

Medical input into indication selection, endpoints, feasibility and protocols, linking the study design to the development question.

The need: A clear clinical question and an evidence plan that can answer it.
How Proxima helps: Consider indication selection, endpoints and feasibility, and contribute to study design and protocols.
Practical value: Connect the study plan to the programme’s development priorities.

Medical monitoring and safety oversight

Support with eligibility, adverse events, protocol deviations, dose escalation discussions and safety committees.

The need: Medical input to the questions that arise during study preparation and trial delivery.
How Proxima helps: Support eligibility review, adverse-event assessment, protocol deviations, dose escalation discussions and safety committees within the agreed role.
Practical value: Keep medical considerations connected to study conduct and safety discussions.

Medical leadership and sponsor oversight

Medical input across internal teams, CROs, trial sites and specialist providers, with clear responsibilities and communication.

The need: Ongoing medical involvement across the people contributing to a clinical programme.
How Proxima helps: Work with internal teams, CROs, investigators and specialist providers to support medical decisions and communication.
Practical value: A clearly defined medical role that complements the existing sponsor team.

Clinical documentation and regulatory support

Medical review and contributions to protocols, investigator brochures, safety documents and clinical study reports.

The need: Clinical documents that clearly explain the study, its medical rationale and its findings.
How Proxima helps: Contribute medical input to protocols, investigator brochures, safety documents and clinical study reports.
Practical value: Support consistency and clinical clarity across the programme’s documents.

Australian trial planning and investigator engagement

Assess trial opportunities and suitable sites, and bring clinical input to planning and investigator discussions.

The need: Clinical input when considering or preparing a study in Australia.
How Proxima helps: Assess trial opportunities and suitable sites, and contribute to planning and investigator engagement.
Practical value: Bring medical considerations into early planning and site discussions.

A practical note: Proxima provides medical and clinical development consultancy. Website content is general information and is not medical, patient-care, legal or definitive regulatory advice.

Shape the right scope

Define the support your programme needs next.

Start with the issue, decision or capacity gap. Proxima can help define a proportionate scope around what the programme needs now.

Discuss your programme Send an enquiry