Involved in study initiation and site set-up, including preparation and maintenance of essential documentation, site files, and regulatory materials. Supported SIVs, liaised with study teams and clinical teams, and ensured readiness for participant recruitment in line with protocol and GCP requirements.

Supported participant identification, screening, recruitment, and ongoing study coordination across multiple studies. Acted as a central point of contact between clinicians, research teams, and participants to ensure smooth study delivery and protocol adherence.

Conducted CRFs, participant interviews, and data collection in accordance with study protocols. Supported monitoring activities, completed protocol deviation documentation, and contributed to maintaining data quality and regulatory compliance throughout study delivery.

Supported study close-out activities, including document reconciliation, data completion, and site file finalisation. Contributed to knowledge transfer and continuity across studies to support audit readiness and future research activity.

• Study set-up

• Recruitment & coordination

• CRFs & interviews

• Monitoring support

• Protocol adherence

• Protocol deviations

• ISF maintenance

• GCP-aligned practice

• Multidisciplinary liaison

• Study close-out

• Phlebotomy trained

• Clinical device use