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.
Apply via :
krb-xjobs.brassring.com
