|
Trials Co-ordinating
Centre (TCC) |
| Tel:
+44 (0) 20 7299 4684 Fax: +44 (0) 20 7299 4663 |
| For email address please visit the individual trial websites by clicking on the logo on the homepage. |
Last updated 17 January 2012
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TCC
Team
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Haleema Shakur Project Director "I have the day to day responsibility for making sure that we have a successful trial, that the trial is conducted to a high standard and to make sure our collaborative group grows. The group we have formed as a result of the MRC CRASH trial is truly unique and I hope that we can build a bigger and more inclusive team for future trials and that we can go on to answer many more clinically important questions in trauma. If you have any suggestions about how we can improve the trial processes for you, please let me know. I look forward to meeting all of you during the course of the trials." |
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Ian Roberts Clinical Co-ordinator "My research interests include the prevention, treatment, and rehabilitation of injury, with the aim of providing rigorous research evidence on which to base intervention strategies." |
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Eni Balogun Regional Coordinator "I am here to help deal with any day to day issues that might arise whilst you're doing the trials; this could be anything ranging from getting ethics committee and regulatory authority approvals to issues impacting on patient recruitment at your hospital. Do get in touch to let me know how we can help make trials easier for you to do!" |
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Danielle Beaumont Regional Coordinator |
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Jamie Brown |
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Taemi Kawahara Responsibility for day-to-day management of the trial. "I work as part of the trial management team to ensure that the WOMAN trial is successful, conducted to a high standard and day to day issues that arise during the trial are resolved. My role as regional co-ordinator also means I work closely with collaborators through the whole process of joining the trial from invitation to recruitment of patients." |
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Katharine Ker Regional Coordinator |
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Lesley Vidaurre Regional Coordinator "As a regional coordinator and assistant trials manager for both the WOMAN and CRASH-3 trials my role is to support sites that are already participating in the trials as well as identifying new sites that would like to take part and guiding them through the approvals process. This includes ensuring that GCP, regulatory and ethical requirements are met. Working with a collaborative team is a very rewarding experience and we want our collaborators to feel as proud of their achievements as we are. If at any time you need any assistance, I would be very happy to help." |
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Elizabeth Woods Regional Coordinator "As an assistant trials manager I am involved with the entire process of our trials including identifying potential sites and progressing regulatory approvals. As a regional co-ordinator I am responsible for monitoring the trial progress in my designated countries and encouraging the recruitment, training and compliance of site teams across the world. I can help with any day to day issues that arise from the conduct of the trial so please get in contact." |
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Lin Barnetson "As data manager my role is to ensure that the trial data are of the highest standard and that any issues arising are satisfactorily resolved. As good data is key to the success of a trial our aim is to provide complete and accurate data sets for analysis so that the trial questions are clearly answered. To do this involves daily communication with you all so please do not hesitate to let us know if you have any problems with, or questions about, data. No problem is too large or too small! Your observations and feedback on data collection are also very welcome as this helps us improve our service so please let us know what works for you and what doesn't. Working together we can deliver the best possible data and robust results." |
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Rob
Jackson Data Manager WOMAN trial |
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Maria Ramos "I have the overall responsibility for the administrative aspects of all our ongoing trials, including budget monitoring and finances, production and distribution of trial treatment and other trial materials, and publicity through newsletters and trial websites. I will be contacting collaborators from time to time for specific requests, such as your hospital specific trial materials, drug related issues or even photographs for newsletters. Do get in touch if you have any specific requests or problems with materials. We are only too happy to help in order to make the day to day activities of the trials go smoothly at your hospital." |
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Collette Barrow Day today administrative procedures; distribution of trial materials and drugs to participating sites; payments. |
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Catherine
Gilliam Trials Assistant |
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Joe Strachan |
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Other
associated people
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Beverley Hunt, King's
College, Guy's & St Thomas' NHS Foundation Trust CRASH-2 trial Management
Group |
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Carine Ronsmans, LSHTM WOMAN trial Management Group |
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Diana Elbourne, LSHTM WOMAN trial Management Group |
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Metin Gülmezoglu,
WHO WOMAN trial Management Group |
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Phil Edwards, LSHTM CRASH-2 trial Management Group |
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Tim Coats, University
of Leicester, Leicester Royal Infirmary CRASH-2 trial Management Group |
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Zarko Alfirevic, University
of Liverpool, Liverpool Women's Hospital WOMAN trial Management Group |