COMMUNITY HEALTH of SOUTH DADE, Inc.
RESEARCH COORDINATOR
COMMUNITY HEALTH of SOUTH DADE, Inc., Miami, Florida, us, 33222
Community Health of South Florida Research Coordinator:
The primary focus of the position is patient/participant recruitment, providing intervention materials, data collection, and data entry. This position is expected to work under general supervision and leadership from the Health Choice Network Research Team and Community Health of South Florida and will help meet specific deliverables with research collaborators at Moffitt Cancer Center, to implement and coordinate a research intervention study, including administrative procedures. The individual in this role will interact with research team members at Health Choice Network, Community Health of South Florida, and Moffitt Cancer Center for guidance and supervision. The individual in this role with interact with patients at Community Health of South Florida sites and will be required to be in-person at the partnering sites multiple days per week. Our team is seeking a responsible, dependable, and detail-oriented individual who will interact with team members and patients in a respectful manner.
Job duties include (but not limited to):
Identify and screen patients for eligibility.Complete informed consent procedures with interested and eligible individuals in English and Spanish.Provide intervention materials to eligible enrolled participants.Document the consent process accurately pursuant to regulatory, Health Choice Network, and Moffitt Cancer Center guidelines.Enter data and other pertinent information into the appropriate databases (i.e., Redcap, EHR or other sponsor specific electronic data capture (EDC) system).Responsible for quality of the data coming in and ensuring that the protocol is being followed appropriately.Ensure participants are provided intervention materials at the correct time points.Responsible for delivering surveys and/or conducting interviews in English and Spanish.Collaborate with study team members.Completing study follow-up with participants according to study protocol.Prepare reports as requested.Qualifications/study needs:
Associate's degree required in field relating to public health, psychology, biological sciences or relevant field with 1 year of relevant research experience.Fluent in both English and Spanish.Have a personal vehicle/valid driver's license and be willing to drive to clinic study sites multiple days per week.
WE ARE AN EQUAL OPPORTUNITY EMPLOYER
The primary focus of the position is patient/participant recruitment, providing intervention materials, data collection, and data entry. This position is expected to work under general supervision and leadership from the Health Choice Network Research Team and Community Health of South Florida and will help meet specific deliverables with research collaborators at Moffitt Cancer Center, to implement and coordinate a research intervention study, including administrative procedures. The individual in this role will interact with research team members at Health Choice Network, Community Health of South Florida, and Moffitt Cancer Center for guidance and supervision. The individual in this role with interact with patients at Community Health of South Florida sites and will be required to be in-person at the partnering sites multiple days per week. Our team is seeking a responsible, dependable, and detail-oriented individual who will interact with team members and patients in a respectful manner.
Job duties include (but not limited to):
Identify and screen patients for eligibility.Complete informed consent procedures with interested and eligible individuals in English and Spanish.Provide intervention materials to eligible enrolled participants.Document the consent process accurately pursuant to regulatory, Health Choice Network, and Moffitt Cancer Center guidelines.Enter data and other pertinent information into the appropriate databases (i.e., Redcap, EHR or other sponsor specific electronic data capture (EDC) system).Responsible for quality of the data coming in and ensuring that the protocol is being followed appropriately.Ensure participants are provided intervention materials at the correct time points.Responsible for delivering surveys and/or conducting interviews in English and Spanish.Collaborate with study team members.Completing study follow-up with participants according to study protocol.Prepare reports as requested.Qualifications/study needs:
Associate's degree required in field relating to public health, psychology, biological sciences or relevant field with 1 year of relevant research experience.Fluent in both English and Spanish.Have a personal vehicle/valid driver's license and be willing to drive to clinic study sites multiple days per week.
WE ARE AN EQUAL OPPORTUNITY EMPLOYER