Overall Responsibility
The
Research Assistant will provide support to the research team in conducting this
study.
Key Responsibilities
- Assist with identifying and screening
potential participants based on inclusion/exclusion criteria and obtain
informed consent from eligible patients or their representatives.
- Collect demographic and clinical data
from medical records, ensure accurate and complete data entry into
designated study electronic databases.
- Track patient progress throughout their
hospital stay while documenting relevant clinical information.
- Assist with scheduling and coordinating
blood draws for thromboelastometry and other required blood tests.
- Proper labelling and storage of blood
samples according to study protocol and assist with sample processing
tasks as required.
- Maintain accurate and organized study
records, enter data into designated study databases in a timely and
accurate manner.
- Maintaining research files and study
documents and help prepare study reports and presentations (as needed).
The Requirements
- Bachelor’s degree in a relevant field
(e.g. Public Health, Nursing, Medical Laboratory Sciences)
- At least 1 year experience in research
experience in clinical research setting
- Strong understanding of research ethics
and informed consent procedures.
- Excellent organizational skills and
attention to detail.
- Ability to work independently and as part
of a team.
- Proficient in computer skills (data
entry, spreadsheet software).
- Excellent communication and interpersonal
skills.
How To Apply
