Research Coordinator - Open Rank

University of Massachusetts Medical School•Worcester, MA
•$40,000 - $60,000

About The Position

Under the direction of the Principal Investigator or designee, the Research Coordinator carries out multiple complex research protocols. The posting describes two open levels: Research Coordinator I and Research Coordinator II. Research Coordinator II performs the duties of Research Coordinator I and takes on additional project, clinical-study, regulatory, and operational responsibilities.

Requirements

  • Research Coordinator I: bachelor’s degree in the sciences or health care, or equivalent experience.
  • Research Coordinator I: one year of related experience.
  • Research Coordinator I: experience using computer-based tools such as Word, Excel, Access, Outlook, and PowerPoint.
  • Oral and written communication skills.
  • Excellent organization, analytical, and interpersonal skills.
  • Ability to travel to off-site locations.
  • Research Coordinator II: requirements for Research Coordinator I, plus a bachelor’s degree in a scientific or health care field, or equivalent experience.
  • Research Coordinator II: three years of related experience.
  • Research Coordinator II: demonstrated knowledge of federal requirements for conducting clinical trials.
  • Research Coordinator II: experience using computer-based tools such as Word, Excel, Access, Outlook, and PowerPoint.

Responsibilities

  • Collaborate with investigators to design, develop, and document data forms, questionnaires, and other survey materials.
  • Contribute to research recommendations and the design of research projects.
  • Participate in grant, manuscript, and Institutional Review Board processes.
  • Develop plans for conducting community surveys and conduct in-person or telephone field research.
  • Monitor participant selection and randomization.
  • Coordinate participant data collection, complete case report forms, and develop and maintain spreadsheets and computerized data files.
  • Collect and maintain questionnaires and other participant data forms.
  • Conduct literature searches and prepare detailed written summaries of findings.
  • Collaborate with project leaders on data presentation, interpretation, and scientific reports.
  • Assist with budget and operational aspects of grant and contract proposals, as applicable.
  • Prepare summary reports and ongoing project evaluations for investigators.
  • May recruit, select, supervise, and direct data collection employees and Research Technicians.
  • Conduct quality-control checks on field data collection systems.
  • Coordinate with other research sites to promote consistency and accurate documentation.
  • For Research Coordinator II: support projects by implementing work plans and preparing deliverables, project-meeting materials, IRB submissions, reports, evaluations, and arrangements such as interviews.
  • For Research Coordinator II: take administrative responsibility for clinical aspects of patient study subjects and testing.
  • For Research Coordinator II: prepare and carry out project-specific surveys, interviews, and focus groups with patients, state agency personnel, and other key informants; record and analyze data and evaluate and update it in relation to protocols.
  • For Research Coordinator II: design and execute protocols and experiments, modify protocols as needed, and potentially lead an independent research project.
  • For Research Coordinator II: oversee development of data-collection instruments, survey tools, and interview guides; perform or oversee data collection, management, and analysis.
  • For Research Coordinator II: assist with writing scientific publications and grants and review literature.
  • For Research Coordinator II: assist multiple principal investigators with the design, development, and implementation of research.
  • For Research Coordinator II: assist with revenue and expense account operations, compile expenses for fiscal reports and grant budgets, and assist with grant reporting requirements.
  • For Research Coordinator II: maintain regulatory paperwork throughout study initiation, continuation, and termination, including IRB applications, informed consents, and HIPAA authorizations.
  • For Research Coordinator II: may recruit, select, supervise, and direct data collection employees, Research Technicians, and Research Coordinators.
  • For Research Coordinator II: comply with applicable safety and infection-control standards and maintain inventory of research-related supplies.
  • Perform other duties as required.
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