End-to-End Regulatory Strategy, Intelligence, and Business Impact Assessment to Support Development and Commercial Decisions

Regulatory Programme/Project Planning, Governance, and Delivery Leadership for Global Portfolios

Regulatory Dossier Strategy, Gap Analysis, and Lifecycle Management Across Regions

Leadership of Global Regulatory Submissions from Initiation through Approval

Medical and Scientific Writing: manuscripts for peer-review, educational and promotional material (ITA, ENG)

Translation of scientific document from English and Spanish into Italian

Editing of scientific documents

Review and fact-checking of scientific documents

Early-stage drug discovery

Platform positioning

Data management and analysis

Startups

Analytical strategy planning and implementation including analytical assay design, optimisation, and validation

Translational medicine support including data preparation for IND/CTA submission and clinical operations

CRO selection and management

GCP-compliant regulatory support, quality management system support, and INC/CTA submission

Press releases 

Media outreach 

MedComm (blogs, articles, newsletters, award applications, abstracts, web copy, social media posts)

Pitch deck optimization (investors meetings, conferences, board meetings)

Scientific data visualization from quantitative and qualitative data sources.

2D scientific illustrations, especially cellular biology and molecular mechanisms.

Graphic materials for screen and print: including annual reports, publications, educational materials, grant graphical abstract.

Audience-tailored communication support.

Strategic Partnering & Deal Delivery (End-to-End)

Portfolio Strategy & Value Optimisation

Licensing Strategy, Structuring & Negotiation

Fundraising & Investor Narrative Development

Scaling support from inception to Series A (fundraising, partnership, pathway)

Strategic guidance to refine business models (go to market, IP)

Operational leadership to bridge science and business

Clinical studies and regulatory pathways (FDA, EMA, NMPA)

Market entry, expansion and growth strategies

Biotech pipeline evaluation and licensing                                

CRO and CDMO manufacturing

Strategic regulatory gap asessment

Regulatory roadmap

Regulatory roadmap implementation

Leadership and business coaching including mentoring for early stage founders

Executive and C-Level Scientific Leadership (Fractional or Interim) 

Translational Strategy and Early Development Planning 

mRNA and Advanced Therapeutics Platform Advisory 

Pipeline, Platform, and Technical Due Diligence for Investors and Biotech Leadership

Early-stage drug development

Regulatory strategy

First-in-human and proof-of-concept studies

Programme management

Clinical operations and portfolio management

Clinical trial and CRO/ site mangement

Service provider selection / management / oversight

People management and coaching / training

Marketing strategies and plans

Marketing messaging audits

Marketing messaging development

Marketing messaging implementation and copy

Regulatory writing (including revision and QC): clinical study protocols, clinical study reports, investigator's brochures, briefing books, CTD

Scientific Writing: drafting/editing/QC of manuscripts for peer-reviewed journals

Strategic business development and innovation management

Strategic copywriting and grant writing for life sciences (websites, LinkedIn, pitch decks, regional/national/EU funding)

Translating research into investor- and industry-ready messaging

Positioning scientists and biotech founders as credible thought leaders

Project management (comms, medcomms)

LinkedIn carousels

Posters

Presentations

Scientific & Business Strategy

Project Leadership & Management

CRO Scoping & Management

Team Building & Operational Support

Scientific strategy and project management in life science in general with focus on translational projects in immunology

Consulting on innovative approaches and ideas in biomedical sciences and TechMed. 

Grant writing and funding support

Start-up pitch and value proposition preparation

Drug discovery strategy, including screening cascade, assay design, in vitro pharmacology, IVIV translation, biomarker strategy

Setting up data analysis/management/archiving, LIMS systems for drug discovery

Commercial/BD strategy and pitch deck preparation

Grant, manuscript preparation and review

Medical and scientific writing 

Localization of educational material from English to Italian

Editing and proofreading of medical, scientific, academic, and regulatory documents, fact-checking

Literature search and reference organization

Medical and regulatory writing 

Scientific and technical writing

Quality assurance and quality control 

Regulatory intelligence

Craft clear, compelling biotech narratives that resonate with stakeholders

Translate complex science into clear, action-driving messaging

Guide communications through change, uncertainty, and growth with clarity and purpose

Facilitate insight-driven workshops that unlock alignment and drive momentum

Expert advisory and support for securing research funding.

Critical proposal review and end-to-end bid development for competitive UK and EU funding schemes.

Grant scouting and interview preparation to support successful applications.

Coaching, training, and bespoke workshops for researchers and teams.

Data stewardship and data management, specializing in R&D chemistry and small molecules data management.

Build efficient data strategies to unlock value for company and department, including change management.

Uncover and engage with all the teams involved to optimize data utilization and problem-solving in data management. 

Propose processes for data analysis and reporting to enhance decision-making

Assay and product development for research tools and diagnostics.

Technical and strategic consulting, including due diligence, independent review and design history file review.

Produc development process design and implementation (ISO 13485, ISO 9001) including risk management (ISO 14971).

Training, coaching and mentoring.

Business strategy for start ups

Quality and regulatory strategy for medtech 

Building executive presence for leaders

Exec coaching for leaders and future leaders

LinkedIn ghostwriting

LinkedIn training and coaching

Content creation strategy and AI generated content

Phase appropriate Quality Assurance 

Hands on approach to developing Quality Systems

Inspection and Remediation Support

Detail oriented documentation writer 

Regulatory strategy for FDA EMA PMDA agency meetings

Review of strategy planning for FDA EMA and Rest of the world Markets

Due diligence

Company structure and process analysis

Support biotech and CGT organizations with site start-up, operational readiness, and tech transfer execution. 

Advise leadership teams on MSAT strategy, GMP manufacturing readiness, and commercialization planning. 

Provide hands-on expertise in deviation management, change control, and process optimization for complex advanced therapy platforms. 

Scientific 2D illustrations and graphics that make complex topics accessible

Expertise in anatomy, surgery, and cellular biology, including drug mechanisms of action

Clear, engaging visuals for websites, scientific publications, and educational materials

Strategic input on how to communicate science effectively through illustration

Clinical project management

Clinical trial management

Clinical operations management

Study and Vendor oversight

Therapeutic antibody strategies, lead optimisation & engineering

Pre-clinical development, assay design & in vivo models 

R&D management, guidance of in-house & outsourced projects

Scientific & technical writing, data overviews, development plans, and pre-IND dossiers

Alliance Management

Project & Program Management

Strategic Support

Scientific due diligence for investors 

Expert analysis of pre-clinical data packages for biotech and pharma

Strategic project leadership in early discovery, preclinical and IND-enabling projects

Writing and review of grant proposals and manuscripts

Strategic leadership of early and late phase oncology and rare disease clinical development programmes.

Chartered statistician - specialising in medical statistics, oncology trial design and endpoint management.

Delivery and outcome focussed oversight and management of vendor and sponsor driven clinical trials.

Biomarker and precision medicine, including EU IVDR.

Vendor selection support including CDMO operational assessment 

CMC project management (during preparation to First-In-Human trial, technical transfer, scale up or process validation)

GMP personalized trainings on demand

Interim team management

Clinical operations management

Clinical trial development, study and site management

Vendor/CRO selection, oversight and management

Fractional leadership and KOL advisory

Provide Strategic Vision, Scientific Direction, and Tactical Oversight to Improve and Accelerate Drug Development Journey

Navigate CMC Technical Development Roadmap and Regulatory Landscape

Support CDMO Evaluation and Selection Process

Oversee and Manage Tech Transfer and cGMP Manufacturing Operations

Process development strategy, optimisation & troubleshooting

CMC strategy, IND/IMPD CMC support, raw material strategy & documentation

Tech transfer & GMP manufacturing oversight

Technical project leadership across ATMP programmes

Organisation development

Human Resources

Dispute settlement

People Strategy

Narrative strategy development & visibility roadmap design for science startups

Founder content creation & thought leadership execution across platforms

Media training & spokesperson development for science-driven founders

Journalist engagement & earned media placement for biotech/health tech