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Clin Rsrch Project Coord I


Job Location:

Pawtucket, RI - USA

Monthly Salary: Not provided by the employer
Posted: 26 August 2026 (26 days ago)
Application Deadline: 4 December 2026
Vacancies: 1 Vacancy

Job Summary

About Us

Care New England Health System (CNE)and its member institutions Butler Hospital Women & Infants Hospital Kent Hospital VNA of Care New England Integra The Providence Center and Care New England Medical Group is a trusted integrated health care organization that fuels the latest advances in medical research attracts the nations top specialty-trained doctors hones renowned services and innovative programs and engages in the important discussions people need to have about their health and end-of-life wishes. Care New England is helping to transform the future of health care providing a leading voice in the ongoing effort to ensure the health of the individuals and communities we serve.

Job Summary

The Clinical Research Project Coordinator I provides supervision and non-clinical administrative support for the project. Responsible for initiating and maintaining recruitment managing daily operations monitoring for continued support for the project. This position coordinates the daily activities assists with processing applicants and tracks the progress of study participants. Maintains data required by sponsors and serves as a resource to all entities/individuals involved in the program. Assists with marketing initiatives and web-site maintenance and ensures compliance with all grant criteria.

Duties & Responsibilities
  • Responsible for the management of research project(s).
  • Trains and supervises project specific staff (Clinical Research Assistants I-III volunteers students consultants etc); records HR issues as needed.
  • Assists in the planning implementation and management of project data.
  • Promotes the project(s) through marketing website other sources etc.
  • Coordinates project meetings including creating agendas and drafting minutes.
  • Collaborates on presentations publications and dissemination of project results as requested.
  • Supervises biospecimen collection packaging shipping and infection control procedures.
  • Aids in preparation of IRB protocols amendments annual reviews risk assessments adverse event reports and informed consent documents; communicates with IRB throughout submission and review process.
  • Supports Investigator in preparing regulatory reports including convening DSMB meetings and writing DSMB reports and assisting with NIH RPPRs.
Requirements
  • Bachelors Degree Required
  • Minimum 1 to 3 Years of experience
  • CCRP CCRA or ACRP-CP preferred
  • Excellent communication skills and analytic abilities
  • Basic computer skills e.g. familiarity with Microsoft software completing spreadsheet/data entry.
  • Ability to work with diverse populations and support an inclusive culturally responsive environment.

Americans with Disability Act Statement: External and internal applicants as well as position incumbents who become disabled must be able to perform the essential job-specific functions either unaided or with the assistance of a reasonable accommodation to be determined by the organization on a case-by-case basis.

EEOC Statement: Care New England is an equal opportunity employer. All applicants will be considered for employment without attention to race color religion sex sexual orientation gender identity national origin veteran or disability status

Ethics Statement: Employee conducts himself/herself consistent with the ethical standards of the organization including but not limited to hospital policy mission vision and values.


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