Purity Bundi
@puritybundi
Global Study Manager delivering early-phase oncology trials across global sponsor, NHS, and academic research settings.
United KingdomWhat I'm looking for
I’m a clinical research professional with over nine years’ experience delivering studies across pharmaceutical, NHS, and academic research environments. I manage international clinical research programmes—supporting multidisciplinary teams and working with investigators, sponsors, vendors, and research sites to deliver studies from start-up through to close-out.
As a Global Study Manager in an early phase oncology sponsor environment, I provide global operational and project leadership across first-in-human, dose-escalation, and dose-expansion designs. I bring structure to complex programmes through strategic planning, risk assessment, regulatory judgement, end-to-end lifecycle oversight, and robust vendor and financial management.
Previously, I served as a Senior Clinical Trial Coordinator at Cambridge University Hospitals, overseeing Early Phase and Imaging Research across high-risk oncology, translational medicine, and imaging portfolios. I also supported grant-funded research (including NIHR, Cancer Research UK, Wellcome Trust, AstraZeneca, and Merck), coordinated COVID-related studies, maintained ICH-GCP and research governance compliance, and later strengthened my foundation in clinical data management and query processes.
Experience
Work history, roles, and key accomplishments
Provided global operational and project leadership for complex early phase oncology development programmes, coordinating safety, data, translational and imaging activities across countries and regions. Oversaw end-to-end study lifecycle delivery and managed vendor-related activities, governance, and compliance.
Senior Clinical Trial Coordinator
Cambridge University Hospitals
Nov 2020 - Aug 2021 (9 months)
Provided operational and governance oversight at portfolio level for early phase and imaging research studies in an academic and NHS environment. Supported Chief Investigators and contributed to grant-funded research delivery, including budgeting, compliance, and oversight of high-risk trials.
Clinical Trial Coordinator
Cambridge University Hospitals
Sep 2018 - Nov 2020 (2 years 2 months)
Coordinated end-to-end delivery of early phase oncology clinical trials, including multi-centre adaptive Phase I–II studies with dose-escalation/expansion designs. Managed study setup, monitoring, compliance, and safety reporting, including trial master file maintenance and regulatory/ethics submissions.
Clinical Trial Data Manager
Cambridge University Hospitals
Sep 2016 - Sep 2018 (2 years)
Managed clinical data for multiple oncology studies, collaborating with participating hospitals to ensure accurate, secure data collection and reporting. Performed study start-up database testing and data management activities including pCRF/eCRF design, coding, safety reporting tracking, and close-out documentation.
Data Associate II
Syne Qua Non
Sep 2015 - Sep 2016 (1 year)
Executed data management activities according to study documentation, contractual requirements, and standard operating procedures. Supported study start-up, QC and testing of clinical databases/eCRFs, data query management, and third-party data reconciliation.
Education
Degrees, certifications, and relevant coursework
University of Huddersfield
Bachelor of Science (Honours), Medical Biochemistry
Completed a BSc (Hons) in Medical Biochemistry at the University of Huddersfield.
Availability
Location
United KingdomAuthorized to work in
Job categories
Skills
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