Clinical Research Consulting Services

Clinical Trials Expert with 19 years of experience in Biotechnology, Pharmaceutical, and CRO companies around the world.

About Us

FR Consulting, based in Australia, specializes in providing clinical trial consulting services to Biotechnology, CROs and Pharmaceutical companies worldwide.

As an independent consulting company, I offer flexible, short- to medium-term support tailored to your project’s specific needs — whether it’s project management, clinical monitoring, or other clinical trial related activities.

My mission is to drive success for both companies and their clinical trials as a skilled extension of their internal teams, ready to step in with hands-on expertise and deliverables that align with company’s goals, timelines, and regulatory expectations.

Clinical Trials – Phase I, II, III & IV

Clinical Operations Services

Clinical Project Manager – Director

All responsibilities from study concept design to CSR Publishing

Develop Study Documents, Tools, plans & more

Development of Protocol, Study plans, tools, forms and guidelines

Expert in Finance Management

Design budget tools and processes, study budget management, forecasting and billing

CTM, Lead CRA, Pharmacovigilance, Regulatory & more

Consulting services across different departments

Clinical Operations Manager

Line Manager Responsibilities for the ClinOps Team

Metrics, KPIs & Risk management

Management and monitoring mechanisms implemented for ongoing supervision

For Clinical Research organisations

Business Development Services

Pre-IND to Phase IV Clinical Trials

Development of SOPs and BD Tools

Improvement or development of BD documents, processes, tools and content for brochures and presentations.

Generating Leads & Building Relationships

Constant engagement with prospects and clients digitally, over the phone and F2F.

Commitment to Excellence

Delivering on time, on budget and at the highest level of quality.

Effective Communication

Interpersonal Communication Skills to interact and listen to the study team, stakeholders and clients effectively.

Attention to Details & Compliance

Clinical Research space is highly regulated, and it involves patient safety above all hence adherence to GCP, Protocol, SOPs and regulatory requirements is essential.

Fabio Romero
Clinical Research Consultant
Mobile: +61 (0) 452 163 007
Email: fabio@frconsulting.com.au