Thomas Jefferson University & Jefferson Health
Research Coordinator - Psychiatry Administration
Thomas Jefferson University & Jefferson Health, Phila, Pennsylvania, United States, 19117
About JeffersonNationally ranked, Jefferson, which is principally located in the greater Philadelphia region, Lehigh Valley and Northeastern Pennsylvania and southern New Jersey, is reimagining health care and higher education to create unparalleled value. Jefferson is more than 65,000 people strong, dedicated to providing the highest-quality, compassionate clinical care for patients; making our communities healthier and stronger; preparing tomorrow#39;s professional leaders for 21st-century careers; and creating new knowledge through basic/programmatic, clinical and applied research. Thomas Jefferson University, home of Sidney Kimmel Medical College, Jefferson College of Nursing, and the Kanbar College of Design, Engineering and Commerce, dates back to 1824 and today comprises 10 colleges and three schools offering
200+
undergraduate and graduate programs to more than
8,300 students.
Jefferson Health, nationally ranked as one of the top 15 not-for-profit health care systems in the country and the largest provider in the Philadelphia and Lehigh Valley areas, serves patients through millions of encounters each year at
32 hospitals campuses
and
more than 700 outpatient and urgent care locations
throughout the region. Jefferson Health Plans is a not-for-profit managed health care organization providing a broad range of health coverage options in Pennsylvania and New Jersey for more than 35 years.Jefferson is committed to providing equal educashy;tional and employment opportunities for all persons without regard to age, race, color, religion, creed, sexual orientation, gender, gender identity, marital status, pregnancy, national origin, ancestry, citizenship, military status, veteran status, handicap or disability or any other protected group or status.Covid Vaccination is a requirement for employment at Jefferson for employees working at Jeffersonrsquo;s clinical entities or at the University. If you are not currently vaccinated you will be required to receive the vaccination prior to hire date if you are offered employment, unless you request and receive an approved medical or religious exemption from Jefferson.Under the direction and supervision of the SBIRT program manager, performs and assists with various tasks pertaining to research activities associated with screening of patients using standardized screening scores, follow-up of patients enrolled in SBIRT program as part of program activities. Assisting Research coordinator I with all program activities like preparation amp; development of training and education material, data management and, research amp; publications related to SBIRT program activities amp; goals.Responsibilities:The Research Coordinator works under limited supervision, assists with running clinical trials, completes regulatory documentation and tracks TJU IRB submission and approvals. May assist in the enrollment of human subjects. May provide clerical and technical support to ensure adherence to research protocols and quality of information received.Performs a variety of research, data base collection and processing, as well as clerical duties in support of clinical program to assist investigators in organizing, gathering and compiling clinical research data.Organizes and maintains documentation required for clinical program.Informs Program Manager/Principal Investigator and/or designated individual on any issues concerning patientsrsquo; response to program services and any communications to amp; from patients.Assists Program Manager/ Principal Investigator with regulatory body filings including IRB submissions.May assist in the enrollment of human subjects.May provide clerical and technical amp; data management support to ensure adherence to research protocols and quality of information received.Education amp; Qualifications Requirements:Associatersquo;s/Bachelor/Masterrsquo;s degree preferred in clinical / para-clinical field, Public Health, Medicine, Behavioral health.1 yr experience in research or clinical tools amp; setting preferred.MS Office suite ndash; Word, PowerPoint, Excel, Visio, SAS/SQL experience/working knowledge preferred.
200+
undergraduate and graduate programs to more than
8,300 students.
Jefferson Health, nationally ranked as one of the top 15 not-for-profit health care systems in the country and the largest provider in the Philadelphia and Lehigh Valley areas, serves patients through millions of encounters each year at
32 hospitals campuses
and
more than 700 outpatient and urgent care locations
throughout the region. Jefferson Health Plans is a not-for-profit managed health care organization providing a broad range of health coverage options in Pennsylvania and New Jersey for more than 35 years.Jefferson is committed to providing equal educashy;tional and employment opportunities for all persons without regard to age, race, color, religion, creed, sexual orientation, gender, gender identity, marital status, pregnancy, national origin, ancestry, citizenship, military status, veteran status, handicap or disability or any other protected group or status.Covid Vaccination is a requirement for employment at Jefferson for employees working at Jeffersonrsquo;s clinical entities or at the University. If you are not currently vaccinated you will be required to receive the vaccination prior to hire date if you are offered employment, unless you request and receive an approved medical or religious exemption from Jefferson.Under the direction and supervision of the SBIRT program manager, performs and assists with various tasks pertaining to research activities associated with screening of patients using standardized screening scores, follow-up of patients enrolled in SBIRT program as part of program activities. Assisting Research coordinator I with all program activities like preparation amp; development of training and education material, data management and, research amp; publications related to SBIRT program activities amp; goals.Responsibilities:The Research Coordinator works under limited supervision, assists with running clinical trials, completes regulatory documentation and tracks TJU IRB submission and approvals. May assist in the enrollment of human subjects. May provide clerical and technical support to ensure adherence to research protocols and quality of information received.Performs a variety of research, data base collection and processing, as well as clerical duties in support of clinical program to assist investigators in organizing, gathering and compiling clinical research data.Organizes and maintains documentation required for clinical program.Informs Program Manager/Principal Investigator and/or designated individual on any issues concerning patientsrsquo; response to program services and any communications to amp; from patients.Assists Program Manager/ Principal Investigator with regulatory body filings including IRB submissions.May assist in the enrollment of human subjects.May provide clerical and technical amp; data management support to ensure adherence to research protocols and quality of information received.Education amp; Qualifications Requirements:Associatersquo;s/Bachelor/Masterrsquo;s degree preferred in clinical / para-clinical field, Public Health, Medicine, Behavioral health.1 yr experience in research or clinical tools amp; setting preferred.MS Office suite ndash; Word, PowerPoint, Excel, Visio, SAS/SQL experience/working knowledge preferred.