Dr Manita Mehmi BSc (Hons) PhD

Institute of Cancer and Genomic Sciences
Trial Coordinator

Contact details

+44 (0)121 414 7611
+44 (0)121 414 3529
Cancer Research UK Clinical Trials Unit
Institute of Cancer and Genomic Sciences
Robert Aitken Building
University of Birmingham
Birmingham B15 2TT

Manita Mehmi is a Trial Coordinator within the Early Drug Development Team at the Cancer Research UK Clinical Trials Unit (CRCTU), Institute of Cancer and Genomic Sciences at the University of Birmingham.

Manita works on the National Lung Matrix Trial, a multi-drug, multi-centre, non-comparative, multi-arm phase II trial in non-small cell lung cancer (NSCLC).


  • PhD in Pharmaceutical Microbiology & Immunology 2009
  • BSc (Hons) in Applied & Human Biology, Aston University, 2005


Manita graduated with a BSc (Hons) in Applied and Human Biology from Aston University in 2005, and completed her PhD in Pharmaceutical Microbiology and Immunology in 2009. 

She started working as a Teaching Assistant at Aston University, where she worked as a personal tutor to undergraduate biology and biomedical science students.  

She then worked as a Research Technician in Diabetes at the  University of Birmingham. Here she was involved in providing technical support to a research programme studying ways of manipulating the immune response to pancreatic islet grafts for the treatment of type 1 diabetes.

Manita subsequently joined the Centre for Liver Research at the University of Birmingham as a Research Technician where she provided technical support to the NIHR funded Liver Biomedical Research Unit. This position required her to assist with assays relevant to clinical trials running within the centre, as well as assisting with administrative tasks related directly to the delivery of the research. In addition, she provided technical support in the running of a cell therapy cleanroom and helped to support the manufacture of cellular vaccines as part of the ImmunoTACE clinical trial.

Manita then joined the Early Drug Development (EDD) team in April 2018 as the National Lung Matrix Trial Coordinator. This involves managing frequent Serious Adverse Event reports; and maintaining professional working relationships with multiple third parties, sites, and pharmaceutical partners.    


Mehmi, M., Marshall, L. J., Lambert, P.A. and Smith, J. C. Evaluation of Disinfecting Procedures for Aseptic Transfer in Hospital Pharmacy Departments. PDA Journal of Pharmaceutical Science and Technology. 63(2): 123-138(2009).