What I do

Study concepts, design options, and protocol synopses grounded in the available evidence. I work with your clinical and statistical specialists to define the research question, study population, and endpoints, and assess whether the proposed study can answer its question.

Protocols, amendments, and investigator brochures, developed from the scientific rationale through to a complete draft. I coordinate input from your team and manage review comments and revisions.

Focused reviews of published research and relevant clinical trials to assess what is known, identify gaps, and inform study decisions. Findings are brought together in an evidence summary with clear implications for the proposed research.

Coordination between sponsors, investigators, CROs, and research partners. I keep timelines, dependencies, review cycles, and agreed actions visible so the team can move the study forward.

Manuscripts, reviews, abstracts, and responses to reviewers. I help translate study findings into clear scientific publications, working directly with the researchers and clinical teams behind the work.