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Profile details
Job category searched
» Health and social professions
» Management
» Production, maintenance, quality
» Services
» Health, pharmacy, hospitals, medical equipment
» Pharmaceutical industry
» Research and development
» Temporary work, recruitment
Professional Experience:
Volunteer in-house monitor
MRC/UVRI/LSHTM
11.2021 - 11.2022
Source data verification,
Trial master file management,
Regulatory affairs management,
Site initiation preparation for new studies.
Interim monitoring,
Study close out.
Start up preparations
QC.QA nurse
MRC/UVRI/LSHTM
08.2019 - 12.2022
Trial master file management.
Regulatory affairs management.
Source data verification,
Staff training and mentorship.
Clinical care Coordination.
Study participant screening and
recruitment.
Bedside nursing.
Critical care nursing.
Planning and managing meetings.
Maintaining communication trails.
Report writing.
Maintaining supplies and inventory.
Trial nurse
Mbale clinical research institute
07.2014 - 12.2017
Screening study volunteers
Obtaining consent.
Randomising consented participants.
Obtaining outcome measurements.
Managing physiological wellbeing.
Offering holistic nursing care.
Communicating patient outcomes including adverse reactions.
Emergency care nursing.
Home followup.
Attending and planning work meetings and dtraining.
Clinical coordination.
Data collection and cleaning
Skills
Electronic Trial master file management.
Electronic source data verification and management.
Electronic and paper data capture and review.
Essential document verification and management.
source data verification.
Adverse event review and reporting
Clinical trial monitoring
Study start up, interim monitoring and close out.
Regulatory affairs management.
Clinical trial Communications.
Training and mentorship.
PowerPoint Presentation and planning.
Risk assessment planning
Education . Master
Master's in Clinical trials
Grace Among
Since 09.2022
Distance learning at London School of Hygiene and Tropical Medicine.
covering modules in: review and reporting in clinical trials.
Clinical trials in practice,
Fundamentals of clinical trials,
Basic statistics in clinical trials.
Project management and coordination,
Regulatory affairs, GCp and ethics,
Protocol development,
Trial design.
CRA post graduate certificate in Clinical Research monitoring, ICH-GCP regulatory management
The CRA training institute Texas, USA
03.2022 - 08.2022
Protocol development,
CRF development, Consent form development, essential document management, electronic trial data management systems.
Source data verification.
Quality control and Assurance.
Site Study qualification assessment and initiation.
Interim monitoring and study close out.
Adverse event reporting.
Problem solving and escalation reporting.
Risk assessment and planning.
Bachelor degree
Cavendish University Uganda
06.2014 - 03.2017
Public health.
Communicable and non communicable diseases.
Health in emergency
Mental health.
Occupational health.
Project planning and management
Health law and. Ethics.
Health education.
Research methods.
Research report writing.
Epidemiology 1 and 2
Biostatistics 1 and 2
Community health among others.
among others
Diploma comprehensive Nursing
Soriti School of Comprehensive Nursing
11.2010 - 11.2013
General Nursing
Midwifery
Domiciliary
Community health nursing.
Languages
english›fluent
german›beginner
More information
immediately
Bwizibwera - Entebbe - Gulu - Hoima - Jinja - Kampala - Kasese - Kira - Lira - Masaka - Mbale - Mbarara - Mukono - Nansana - Rest of Uganda - International
Masaka
Permanent contract - Fixed-term contract - Temporary work - Internship - Freelance - Cooperative Education Program - Part-time work
15.04.2023
33
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