Planning a clinical programme
Clarify the development question, consider the evidence needed and shape a study that can answer it.
Independent medical & clinical consulting
Medical leadership and clinical development support,
tailored to your programme.
Proxima Clinical Consulting supports biotechnology companies, pharmaceutical companies and CROs with clinical development, medical monitoring and sponsor medical oversight.
Support shaped around your teamFocused adviceDefined projectsOngoing medical involvement
When to involve Proxima
The right input.
At the right stage.
Bring in medical expertise for a specific question, a defined piece of work or continuing involvement as your programme develops.
Preparing or running a trial
Add medical input to study preparation, participant eligibility and the safety questions that arise during delivery.
Needing ongoing medical leadership
Connect medical decisions across your internal team, CRO, investigators and specialist providers.
Our services
From the development question
to the clinical detail.
Five connected areas of support. A scope agreed around your programme, priorities and existing team.
Clinical development strategy and study design
Medical input into indication selection, endpoints, feasibility and protocols, linking the study design to the development question.
Medical monitoring and safety oversight
Support with eligibility, adverse events, protocol deviations, dose escalation discussions and safety committees.
Medical leadership and sponsor oversight
Medical input across internal teams, CROs, trial sites and specialist providers, with clear responsibilities and communication.
Clinical documentation and regulatory support
Medical review and contributions to protocols, investigator brochures, safety documents and clinical study reports.
Australian trial planning and investigator engagement
Assess trial opportunities and suitable sites, and bring clinical input to planning and investigator discussions.
How we work
Direct involvement.
A clearly defined role.
Work directly with Dr Nabil Nathie, with an agreed scope and clear responsibilities alongside your existing team.
- 01
Start with the question
Discuss the programme, the decision ahead and where medical input would be most useful.
- 02
Agree the scope
Define the work, responsibilities and timing—whether focused advice, project support or ongoing involvement.
- 03
Work with your team
Stay close to the clinical detail and maintain clear communication as questions and priorities evolve.
The person behind Proxima
Dr Nabil Nathie
Director, Proxima Clinical Consulting
His medical background informs a practical approach to clinical development, medical monitoring and sponsor oversight.
About Proxima ↗Begin a conversation
What does your programme need next?
Discuss whether focused advice, project support or ongoing medical involvement is the right fit.
Discuss your programme