University of Massachusetts Medical School
Research Coordinator I
University of Massachusetts Medical School, Shrewsbury, Massachusetts, us, 01546
Overview
GENERAL SUMMARY OF POSITION:
Under the direction of the Principal Investigator or designee, the Research Coordinator I is responsible for carrying out multiple complex research protocols.
At Lifeline for Families, we develop and scale practical approaches to integrating mental healthcare into perinatal, infant, and child healthcare. We develop, implement, and test scalable models of care, trainings, and tools that support families, regardless of what professional or setting they present to. Lifeline for Families is a mission-based, women-led organization which supports parents (all child caregivers) and their children in their relationship with one another in traditionally adult- or child-centric settings. We promote mental health for parents and/or children through social connections, trust, and nurturing. Lifeline for Families has two programs: Lifeline for Moms, which drives innovative solutions to addressing multi-level barriers (patient, clinician, practice, population, and policy levels) to perinatal mental health care, and Lifeline for Kids, which addresses the impact of trauma on children and families while simultaneously promoting protective factors, operating under the principle of “you don’t have to be a therapist to be therapeutic.” These programs are synergistic with each other; together, we work to create a holistic landscape of trauma-informed family care with an equity lens.
The Research Coordinator I will work primarily on a project funded by the Patient-Centered Outcomes (PCORI). This project, Pathways for Perinatal Mental Health Equity (Pathways), is a clinical trial that is being conducted at Lifeline for Families.
The Research Coordinator I for the Pathways project will:
Participate in qualitative and quantitative data collection and storage.
Assist the study team with the creation and dissemination of materials for project team meetings and activities.
Work closely with all investigators to coordinate project activities and adhere to project work plans.
Coordinate communication with all collaborators on the project, including participants, research staff, project personnel, and representatives from PCORI and support these relationships via active communication.
Responsibilities MAJOR RESPONSIBILITIES:
Collaborate with investigators in the design, development, and documentation of data forms, questionnaires, and other survey materials
Responsible for aspects of the development of research recommendations and the design of research projects
Participate in the grant, manuscript, and Institutional Review Board process
Develop overall research plan for conducting surveys in the community
Conduct in-person or telephonic field research
Monitor selection and randomization process of study participants
Coordinate data collection of study participants, complete case report forms, and develop and maintain spreadsheets
Collect and maintain questionnaires and other data forms from study participants
Perform literature searches and write detailed written summaries of the findings
Collaborate with other project leaders on data presentation, interpretation and writing of scientific reports
Develop and maintain computerized data files for all data to be collected
May assist with budget /operational aspect of grant and contract proposals
Prepare summary reports and ongoing project evaluations for investigators
May help recruit, select, supervise and direct the activities of data collection employees and Research Technicians
Conduct quality control check on field data collection system
Collaborate with other research sites to insure consistency between research sites and accuracy of documentation
Perform other duties as required.
ADDITIONAL RESPONSIBILTIES:
Collect and disseminate questions from the data collection teams for discussion to ensure consistent data collection practices
Create and maintain standard operating procedure (SOP) documents for quantitative and qualitative data collection.
Assist with running analytics, compiling data, and drafting reports
Assist with drafting content, formatting and releasing e-newsletters
Request and collect data required for reports to funders
Attend local and/or national conferences
Qualifications REQUIRED QUALIFICATIONS:
Bachelor’s degree in the sciences, health care, or equivalent experience
1 year of related experience
Experience in using computer-based tools (Word, Excel, Access, Outlook, PowerPoint, etc.)
Oral and written communication skills
Excellent organization, analytical, and interpersonal skills required
Ability to travel to off-site locations
PREFERRED QUALIFICATIONS:
Previous experience with REDCap databases
An interest in healthcare research
Previous experience with qualitative research
SUPERVISION RECEIVED :
Under the direction of the Principal Investigator or designee
SUPERVISION EXERCISED:
May supervise and direct the activities of data collection employees and Research Technicians
ENVIRONMENTAL WORKING CONDITIONS:
Usual office environment, laboratory, medical, surgical, and off campus study sites
Under the direction of the Principal Investigator or designee, the Research Coordinator I is responsible for carrying out multiple complex research protocols.
At Lifeline for Families, we develop and scale practical approaches to integrating mental healthcare into perinatal, infant, and child healthcare. We develop, implement, and test scalable models of care, trainings, and tools that support families, regardless of what professional or setting they present to. Lifeline for Families is a mission-based, women-led organization which supports parents (all child caregivers) and their children in their relationship with one another in traditionally adult- or child-centric settings. We promote mental health for parents and/or children through social connections, trust, and nurturing. Lifeline for Families has two programs: Lifeline for Moms, which drives innovative solutions to addressing multi-level barriers (patient, clinician, practice, population, and policy levels) to perinatal mental health care, and Lifeline for Kids, which addresses the impact of trauma on children and families while simultaneously promoting protective factors, operating under the principle of “you don’t have to be a therapist to be therapeutic.” These programs are synergistic with each other; together, we work to create a holistic landscape of trauma-informed family care with an equity lens.
The Research Coordinator I will work primarily on a project funded by the Patient-Centered Outcomes (PCORI). This project, Pathways for Perinatal Mental Health Equity (Pathways), is a clinical trial that is being conducted at Lifeline for Families.
The Research Coordinator I for the Pathways project will:
Participate in qualitative and quantitative data collection and storage.
Assist the study team with the creation and dissemination of materials for project team meetings and activities.
Work closely with all investigators to coordinate project activities and adhere to project work plans.
Coordinate communication with all collaborators on the project, including participants, research staff, project personnel, and representatives from PCORI and support these relationships via active communication.
Responsibilities MAJOR RESPONSIBILITIES:
Collaborate with investigators in the design, development, and documentation of data forms, questionnaires, and other survey materials
Responsible for aspects of the development of research recommendations and the design of research projects
Participate in the grant, manuscript, and Institutional Review Board process
Develop overall research plan for conducting surveys in the community
Conduct in-person or telephonic field research
Monitor selection and randomization process of study participants
Coordinate data collection of study participants, complete case report forms, and develop and maintain spreadsheets
Collect and maintain questionnaires and other data forms from study participants
Perform literature searches and write detailed written summaries of the findings
Collaborate with other project leaders on data presentation, interpretation and writing of scientific reports
Develop and maintain computerized data files for all data to be collected
May assist with budget /operational aspect of grant and contract proposals
Prepare summary reports and ongoing project evaluations for investigators
May help recruit, select, supervise and direct the activities of data collection employees and Research Technicians
Conduct quality control check on field data collection system
Collaborate with other research sites to insure consistency between research sites and accuracy of documentation
Perform other duties as required.
ADDITIONAL RESPONSIBILTIES:
Collect and disseminate questions from the data collection teams for discussion to ensure consistent data collection practices
Create and maintain standard operating procedure (SOP) documents for quantitative and qualitative data collection.
Assist with running analytics, compiling data, and drafting reports
Assist with drafting content, formatting and releasing e-newsletters
Request and collect data required for reports to funders
Attend local and/or national conferences
Qualifications REQUIRED QUALIFICATIONS:
Bachelor’s degree in the sciences, health care, or equivalent experience
1 year of related experience
Experience in using computer-based tools (Word, Excel, Access, Outlook, PowerPoint, etc.)
Oral and written communication skills
Excellent organization, analytical, and interpersonal skills required
Ability to travel to off-site locations
PREFERRED QUALIFICATIONS:
Previous experience with REDCap databases
An interest in healthcare research
Previous experience with qualitative research
SUPERVISION RECEIVED :
Under the direction of the Principal Investigator or designee
SUPERVISION EXERCISED:
May supervise and direct the activities of data collection employees and Research Technicians
ENVIRONMENTAL WORKING CONDITIONS:
Usual office environment, laboratory, medical, surgical, and off campus study sites