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Expert Profile
Rebecca Kemble
Freelance Consultant, Acclaim Biomedical Consulting Ltd
Rebecca Kemble is an experienced senior Clinical Research Professional and has worked for over 10 years, with a leading global Orthopaedic Medical Device manufacturer. During this time gained significant experience in International Post Market Clinical Follow-up and Regulatory Studies. During this time she was a Project Manager for a number of studies;; focusing on study design, recruitment and selection, study conduct, data analysis, writing reports, and liaison with Investigators/Surgeons.
More recently Rebecca has worked for a Clinical Research Organisation (CRO) covering a wide variety of therapeutic areas including Oncology, CVD, COPD, Alzheimer’s disease, Rheumatoid Arthritis, Epilepsy, Multiple Sclerosis, and Cystic Fibrosis.
Rebecca gained a PhD in 2010 which investigated the impact of antioxidants on intestinal cancer.
Trainings by Expert
Overview of Medical Device Regulation in Europe
Category:
Medical Devices
How to write a Clinical Evaluation
Category:
Clinical Research