Program Monitor Recruitment.
About MRC/ UVRI and LSHTM Uganda Research Unit

The Unit is an internationally recognised centre of excellence with dominant research themes in the areas of HIV and emerging infections, vaccines and immunity, and chronic diseases and cancer. Through a multidisciplinary approach, intersecting basic science, epidemiological research, social-behavioural research and the conduct of new intervention evaluation studies, the Unit contributes knowledge on changing epidemics and diseases, the evaluation of innovative health care options, treatment and prevention and the development of health policy and practice in Africa and worldwide. Following the signing of strategic transfer agreements between the London School of Hygiene & Tropical Medicine (LSHTM) and the Medical Research Council (MRC UK), the Unit formally joined LSHTM on 1st February 2018. The exciting new partnership will boost research capacity into current and emerging health issues in Africa and throughout the world. The Unit is based at the UVRI Entebbe campus with established outposts in Kalungu, Masaka, Wakiso and Kampala Districts. The Unit is now seeking enthusiastic and experienced individuals to fill the following position above.
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Name *
Email *
Gender *
Age *
Phone number *
Current Location of Residence *
Nationality *
If Other, Please Specify
Have you Applied to the Unit Before? *
Select Your Highest level of Academic Qualification. *
If other, Please specify.
Please Specify Your  Highest Acadamic Qualification e.g Diploma in Counselling.
Graduation Year
MM
/
DD
/
YYYY
State any Other Qualification you have Attained.
Years of Experience Working in Clinical Practice. *
Years of Experience Working in a Clinical Research Setting. *
Years of Experience Working in a Clinical Research Setting Monitoring a Medical Research Study. *
Years of Experience Working in a Clinical Research Setting Monitoring an NCD Study. *
Years of Experience With the Following;   *
Less than 1 Year
1 Year
2 Years
3 Years
4 Years & Above
5 Years & Above
None but Willing to Learn
Development of SOPs
Randomised clinical trials
Implementing study protocols
Report Writing
Drafting & sharing monitoring reports
Managing post-monitoring activities
Conducting training
Protocol deviation documentation
Tracking of research-staff CVs, GCP, HSP, SOP and protocol-specific trainings
Review of protocols
Do you have an Updated Practicing Licence? If your Response is "Yes i have", Please Attach it to the Application Documentation. *
Do you have a Certificate and Knowledge in GCP Guidelines for Human Research? If Yes to Both Please Attach a Certificate to the Submitted Documents. *
Do you have a thorough understanding of local and international research guidelines.   *
If your response to the above is "yes" or "Fairly", please list some of the guidlines you know of. *
Current /Most Recent Employer. *
Position Current /Most Recently Held. *
Years of Service with Current /Most Recent Employer. *
Years of Service with Your Previous Employer. *
Current Salary Earning (State Salary After Tax). *
Salary Expectation (State Salary After Tax). *
How Soon Can You Start Work? *
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