Behavioral Research Coordinator II - Adolescent Medicine
2 weeks ago(1/7/2019 3:44 PM)
Behavioral Research Coordinator II – Adolescent Medicine: Based on specific research program needs, patient facing vs. data administrative responsibilities will vary. Coordinates all clinical research activities with moderate supervision.
Conducts quality assurance activities.
Conducts study start-up activities and prepares and maintains all regulatory documents required by sponsor and/or regulatory agencies.
Prepares protocols, informed consent documents,
modifications, renewals and other necessary documents for review by the IRB and/or sponsor and trains staff on protocol/procedures
Coordinates study conduct with other departments to effectively implement behavioral research projects; obtains required letters of support and/or approvals as needed (i.e., IBC, SRC, etc.) and protocol is followed.
Identifies and recruits eligible study subjects; conducts informed consent/assent process.
Arranges and conducts behavioral research visits including delivering behavioral interventions when appropriate.
Attends appropriate research meetings.
Abstracts data from medical records and enters medical information/data onto protocol specific case report forms, study flow sheets, and other required study forms; prepares abstracted/coded data for processing/analysis.
Coordinates reimbursement of subjects.
Collects specimens from subjects and processes specimens or works with Research lab to ensure samples are processed/sent out correctly when appropriate
Records data on source documents and CRFs and/or electronic web based systems.
Monitors/assesses adverse events and reports them as required.
Adheres to research protocol in compliance with applicable institutional, local and federal regulations (OHRP, FDA, GCP, etc.)
Functions as participant liaison for study questions, billing issues, etc.
Maintains all study documents (regulatory binders, source documents, correspondence, etc.)
Promotes the ethical conduct of research by actively participating in research related educational meetings/conferences
Performs job functions adhering to service principles with customer service focus of innovation, service excellence and teamwork to provide the highest quality care and service to our patients.
QA/QC checks for database validity and data monitoring.
Tracking deadlines for grants/deliverables.
Conducts statistical analysis under PI supervision
High School Diploma with three to five years research experience -or-Bachelors with one to three years research experience.
Combination of education and/or experience may be considered in lieu of the degree when the experience is directly related to the duties of the job
Associates /two years of College with two to four years research experience –or-
Knowledge of research regulations preferred.
Good clinical practices documentation required.
Familiarity and experience with IRB regulatory requirements preferred.