This program provide volunteer with hands-on experience in the Clinical Trials Research and Sudies, Building manners and professional values, and clinical insight under the mentorship of certified professionals.
Responsibilities
- Work as clinical research coordinator Or assistant under a direct supervision of the section precept.
- Participate in the design and execution of clinical research projects as applicable.
- Assist in performing data collection and statistical analysis as applicable.
- Participate in collecting clinical samples, recording vital signs and ensuring that all related forms and documentation are complete.
- Assist in performing project communications and recordkeeping as applicable.
- Assist in working as a liaison between the study patients and other members of the research team.
- Assist in arranging and scheduling patients visits for evaluation and assessments as applicable.
- Assist in assist in compiling all relevant patients’ information and data as applicable.
- 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 bachelor 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).
- Submit the Health Screening Form.
- Able to volunteer for 6 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
