This program provides a great opportunity to gain experience in various aspects of research, such as managing and organizing clinical research activities.
Responsibilities
- Participates in clinical research study activities based on the study protocol, such as, schedule patients for study procedures, coordinate drug orders, coordinate laboratory procedures.
- Assist in obtaining informed consent form.
- Assist in data collection and analysis.
- Assist in development of the study forms.
- Provide assistance and support to principal investigator as applicable.
- Work as a research technician under the direct supervision of the section preceptor.
- Assist in collecting, processing, and preparing samples as applicable.
- Participate in all related laboratory tasks and duties as needed.
- Assist in performing lab experiments under the direct supervision of the section preceptor.
- Follow all Hospital related policies and procedures.
- Adhere to all Safety and Infection control practices.
*The above responsibilities are subject to change according to the operational needs and assigned based on volunteer's qualifications.
Eligibility
- Must have a bachelor’s degree in one of the following:
- (Medicine, Public Health, Epidemiology, Nursing, Pharmacy, Respiratory Therapy, Medical Technology in Clinical Laboratory Sciences, Microbiology, Biology, Biochemistry, Chemistry, Toxicology, Biotechnology or related field).
- Completed one certificate related to clinical research such as Good Clinical Practice (GCP).
- Proficient in English language.
- Submit the Health Screening Form.
- Able to volunteer for (8) weeks.
- Adhere to the following business hours from Sunday - Thursday:
- Working hours: 08:00 am – 04:00 pm * expect Thursdays: 08:00 am - 03:00 pm
