- Dagenham, GB
- £20 /hr
- Available now
I am a Researcher and quite flexible with the topics. I am excellent at report writing and designing project plans. I also write and so can ghost write on most topics.
My fieldmore...I am a Researcher and quite flexible with the topics. I am excellent at report writing and designing project plans. I also write and so can ghost write on most topics.
My field is primarily sexual health and so am more that able to design presentations for sexual health eduacation as well as research further into any aspect in this field, including HIV.
Area Covered: London
Work Experience Summary: WORK EXPERIENCE:
19/06/08-03/07/08 Clinton Foundation (Clinton HIV/AIDS Initiative), Nigeria
Quantification ; I was responsible for creating a database to hold updated data on paediatric drug distribution to the different sites in Nigeria
11/07-03/08 Newham General Hospital, London
Temp Work • Data Entry in Medical Records
24/07/07 • 30/10/07 Department of Health, London
Improvement Review (MRSA) Support Officer Key Duties include:
Improvement Programme plan management
Providing secretarial support to team meetings
Database and Document management
Providing Admin support for the Improvement Programme team and using excel spreadsheet to show progress with
Getting teams together to go on site visits.
09/06 • 12/06 Rotherham Primary Care Trust
Health Promotion (unpaid post). Key duties included:
Writing a draft Obesity Strategy
I set up power point presentations for Health Promotion Trainers to use in training
Assisting the sexual health team in the Chlamydia tender, as well as researching for, and writing up the sexually transmitted diseases section of the sexual health strategy
2003 - 2004 Charterhouse Clinical Research Unit, London
(Placement Year) Clinical Trials Assistant Key duties included:
Pharmacokinetic sample collection; processing and testing for drugs of abuse as well as biochemistry and serology testing
Processing case report forms (CRFs) and maintaining study files for each project
Keeping study director informed of study progress
Preparing Ethics and Regulatory affairs submissions with Clinical Research Associates
I demonstrated that I could mentor and help new CTAs where necessary
Extensive involvement in screening volunteers and point of care devices
I showed ability to work as part of a team and according to protocol. I also demonstrated an appreciation for confidentiality in the handling and processing of data.
06/04 • 07/04 Clinical Trials Laboratory Services, London
Haematology Lab Technician Key duties included:
Calibrating and loading samples on the H3 machine, and sending results to different health centres that required them.
Education Summary: Masters in Public Health, (MPH)
University of Sheffield
Modules included: Public Health Sociology
Epidemiology Needs Assessment
Health Promotion Research Methods
Using Routine Information
Dissertation Title: Aspirin and Prevention of Breast Cancer: A Systematic Review
2001 • 2005 BSc (Hons) Biomedical Science,
Sheffield Hallam University
Modules Included: Pathology Microbiology
Immunological Basis of Disease