Research Coordinator (Be Well Research)
Job
Summary:
Under general supervision, responsible for providing specialized administrative support in a laboratory and/or clinical research environment.
Job Duties:
Coordinates multiple research protocols and grant submissions.
Assists with monitoring budgets, spending, purchasing, and participant payments.
Creates, completes, and tracks forms and reports for study sponsors.
Schedules on-site visits or meetings and prepares agendas as indicated.
Provides routine technical/administrative assistance in performing assigned and delegated tasks in support of research projects to ensure continuous clinical research operations.
Maintains research subject files for each clinical study and enters all subject data into a research database.
Monitors ongoing activities on various research studies to ensure compliance with local, state & federal regulations.
Serves as research study subject recruiter, interviewer, screener, and evaluator of candidates for studies.
May perform study procedures as per the study protocol.
Performs all other duties as assigned.
Education:
Bachelor's degree in a related field is required.
Experience:
Three (3) years of progressive experience in grant administration, research coordination, data collection, and/or facilitating the patient experience in research projects is required.
Recommended Skills Administration Agenda Development Clinical Research Coordinating Data Collection Financial Management Estimated Salary: $20 to $28 per hour based on qualifications.
Summary:
Under general supervision, responsible for providing specialized administrative support in a laboratory and/or clinical research environment.
Job Duties:
Coordinates multiple research protocols and grant submissions.
Assists with monitoring budgets, spending, purchasing, and participant payments.
Creates, completes, and tracks forms and reports for study sponsors.
Schedules on-site visits or meetings and prepares agendas as indicated.
Provides routine technical/administrative assistance in performing assigned and delegated tasks in support of research projects to ensure continuous clinical research operations.
Maintains research subject files for each clinical study and enters all subject data into a research database.
Monitors ongoing activities on various research studies to ensure compliance with local, state & federal regulations.
Serves as research study subject recruiter, interviewer, screener, and evaluator of candidates for studies.
May perform study procedures as per the study protocol.
Performs all other duties as assigned.
Education:
Bachelor's degree in a related field is required.
Experience:
Three (3) years of progressive experience in grant administration, research coordination, data collection, and/or facilitating the patient experience in research projects is required.
Recommended Skills Administration Agenda Development Clinical Research Coordinating Data Collection Financial Management Estimated Salary: $20 to $28 per hour based on qualifications.
|
|
 | |
