Sophia Jenkinson
About Sophia Jenkinson
Sophia Jenkinson is a Clinical Trial Manager at Bristol Myers Squibb in London, with extensive experience in clinical research and trial management across various organizations.
Title and Current Role
Sophia Jenkinson currently holds the position of Clinical Trial Manager at Bristol Myers Squibb in London, England, United Kingdom. In this role, she oversees clinical trial protocols and ensures adherence to regulatory guidelines and operational continuity. She collaborates closely with stakeholders, including Medical Monitors, Protocol Managers, and Clinical Data Quality Managers, to ensure the timely execution of trial activities.
Past Positions and Experience
Sophia Jenkinson has extensive experience in the clinical trial industry. Her career includes roles such as Project Manager at Medical Research Network from 2020 to 2021 and Project Manager Associate from 2019 to 2020. Earlier, she worked at Research Organisation (KC) Ltd as a Senior Clinical Trial Associate from 2018 to 2019. She has also held positions at Imperial College London, King's College London, UCL Cancer Institute, Royal National Orthopaedic Hospital NHS Trust, The Portland Hospital for Women and Children, University College London, and Ultrasound Direct.
Clinical Research Skills and Responsibilities
Sophia Jenkinson possesses a comprehensive understanding of complex clinical protocols, targeted endpoints, and ICH-GCP guidelines. She regularly conducts eTMF review and maintains AE/SAE oversight to ensure compliance and inspection readiness. She is skilled in managing startup, ongoing, and closeout activities at both site and country levels for early-phase oncology and GMO studies. Additionally, she provides guidance to sites and monitors through close stakeholder collaboration.
Compliance and Regulatory Adherence
Ensuring that clinical trial activities comply with study timelines, ICH-GCP guidelines, and local regulatory standards is a key part of Sophia Jenkinson's role. She identifies potential issues at site or protocol levels and suggests resolutions to maintain study progress. Moreover, she disseminates critical information to Bristol Myers Squibb team members to uphold program-level standards, ensuring that site management activities and study documentation meet all compliance requirements.