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DescriptionIn the Longitudinal Research Program in Late-Life Suicide, Our research lab seeks to understand the interacting risk and protective factors related to biological and psychosocial factors of aging that lead to the elevated suicide rate in late life. We conduct a longitudinal study of late-life suicide attempters, which provides a unique opportunity to evaluate the predictive value of these risk factors on prospectively assessed suicidal behavior. Currently over 600 participants contributed to our unique dataset. In addition to our detailed clinical characterization (DSM diagnoses, personality traits, suicide history) we use neurocognitive assessments, game theory experiments, and decision process measures to understand how cognitive abilities and decision making contribute to suicide risk. More information about the lab’s research can be found at gsuicide.pitt.edu. The Research Coordinator will primarily assist with training on diagnostic interviews, mood, behavioral, and neuropsychological assessments and, self-administer some assessments and be responsible for reliable administration and data entry. All team members attend weekly enrichment meetings discussing research in the field. They may also attend the inpatient psychiatric unit in order to conduct assessments. Applicants with both Bachelor and Master’s degree are encouraged to apply. The ideal candidate has experience working with populations with mental or emotional health diagnoses and has experience with diagnostic interviews and neuropsychological assessments. The candidate may also have an interest in or experience with data management, with many on the job opportunities to learn more about advanced data management.This position is grant funded.Purpose:This position is for a casual Research Coordinator involved in patient-related studies. This position will involve overseeing junior staff, training junior staff, contact with study participants, scheduling appointments, administering research questionnaires, follow-up of study participants, collecting, entering and verifying data, assisting in quality control procedures and general clinical research assistance.Responsibilities:Perform duties for approved research projects according to defined protocols and procedures including appropriate collection, recording, and storage of data.
Assist in collection, data analysis and data presentation and publication.
Assist in data collection and data entry and quality control of data.
Administer questionnaires, and assist with procedures for obtaining patient screening and recruitment as well as obtaining data.
Follow appropriate research policies and procedures including all applicable laws and regulations and maintains scientific integrity including accurate data storage.
Follow the mandatory reporting procedures for any incident or serious event that did affect or potentially could have affected the clinical care of any patient.
Coordinate the daily activities and special projects for department.
Coordinate scheduling of assessments.
Assist with quality assurance over all aspects of data collection and management, including data flow, data entry and verification, maintenance of all project databases, data security and confidentiality.
Provides regular supervision for junior staff.
Communicate effectively with the research, clinical, and administrative staff related to this research.
Coordination of recruitment ie. Advertisements, tracking recruitment, and developing strategies to increase response in targeted populations.
Responsible for the submission of regular reports detailing the progress of the research, including NIH progress reports.
QualificationsB.A. degree, or equivalent combination of experience and training - including 3-5 years of experience in coordinating multiple aspects of research projects (patient recruitment, assessment, treatment planning, and data collection,) required.
Experience working or volunteering with populations with mental or emotional health diagnoses preferred.
Experience with Redcap or other data management preferred.
Experience with diagnostic interviews and neuropsychological assessments preferred.
Computer Skills (Microsoft Office Products).
IRB experience preferred.
Ability to accurately collect, and store research data.
Excellent communication skills both verbal and written.
Demonstrated ability to effectively communicate with patients, staff and investigators as well as maintain patient confidentiality.
Strong organizational skills.
Ability to work independently, must be able to work a flexible schedule based on study needs.
Ability to interact with patients/study participants and research and medical staff.
Knowledge of the principles of growth and cognition over the life span and possess the ability to assess data reflective of the patient's status and interpret the appropriate information needed to identify each patient's requirements relative to his/her age specific needs and to provide the care needs as described in the department's policy and procedures.
Licensure, Certifications, and Clearances:Act 34 with renewal
UPMC is an Equal Opportunity Employer/Disability/VeteranREQNUMBER: 555449207
Vacancy expired!