Clinical Research Coordinator jobs in Rhode Island
Clinical Research Coordinator organizes research information for clinical projects. Selects and observes subjects and assists with data analysis and reporting. Being a Clinical Research Coordinator oversees experiment scheduling and collection of data. Requires a high school diploma or equivalent. Additionally, Clinical Research Coordinator typically reports to a supervisor or manager. The Clinical Research Coordinator works under moderate supervision. Gaining or has attained full proficiency in a specific area of discipline. To be a Clinical Research Coordinator typically requires 1-3 years of related experience. (Copyright 2024 Salary.com)
Recently Added Clinical Research Coordinator jobs
Clinical Research Coordinator - Open Rank
- UMass Chan Medical School
-
Lincoln, RI
FULL_TIME
-
POSITION SUMMARY:
Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator is responsible for independently performing delegated tasks and procedures involving human subject research. This work includes coordination of regulatory activities and aspects of collection and management of data for research protocols related to treatment, ancillary services, and prevention practices.
This is an open-rank posting (there are 4 levels of Clinical Research Coordinator) - candidates will be hired into the level commensurate with their experience.
ESSENTIAL FUNCTIONS:
Clinical Research Coord I:- Obtain consent of research participants in accordance with the IRB approved protocols and all applicable regulations including HIPAA
- Identify, schedule and/or conduct participant study visits, tests and/or interviews/telephone follow up calls
- Coordinate participant remuneration/compensation per protocol
- Maintain all regulatory documentation, including local or central IRB and study data. Provide data/support to study Investigators, sponsors and/or external monitors/auditors
- Identify issues with protocol compliance. Keep principal investigator and manager aware of any issues regarding compliance
- Document and collect data and/or samples for research related procedures performed during participant study visits.
- Ensure clinicians and/or PI accurately document their study activities according to protocol
- Track and maintain study enrollment and completion of milestones
- Assist with financial /operational aspects of grant and contracts. May be responsible for clinical research billing review within the required timeframe.
- Track and maintain study related information in the data management system within the required timeframe
- Responsible for monitoring the inventory of research related supplies
- Participate in grant preparation, manuscript writing, data presentations and Institutional Review Board (IRB) processes
- Provide detailed written summaries from literature searches and related sources to serve as a resource for the study team and clinicians/PIs
- Present study status reports related to assigned research projects
- Participate in the design, development, and documentation of study related data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)
- Maintain strict adherence to all study protocols, including all regulatory requirements adhering to appropriate federal, local and institutional guidelines.
- Comply with all safety and infection control standards appropriate to this position
- Adhere with established policies, health and safety regulations and requirements, procedures, and department objectives
- Adhere to Good Clinical Practice (GCP) guidelines and all human subject protection practices
- Must practice discretion and adhere to school and hospital confidentiality at all times
- Perform other duties as required.
Duties Noted Above Plus:- Conduct preliminary quality assurance reviews of study data
- Contribute to data presentations and Institutional Review Board (IRB) processes
- Track and maintain study related information in the data management system within the required timeframe
- Contribute to the design, development, and documentation of study related data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)
- Document and collect data/ samples for research related procedures performed during participant study visits. Ensure clinicians and/or PI accurately document their study activities according to protocol.
- Monitor strict adherence to all study protocols, including all regulatory requirements adhering to appropriate federal, local and institutional guidelines. Identify and resolve issues with protocol compliance. Keep principal investigator and manager aware of any issues regarding compliance
Duties Noted Above Plus:- Assist with recruiting, screening, selecting, maintaining and terminating study subjects for multiple protocols
- Ensure accuracy and completion of all regulatory documentation, including local or central IRB and study data. Provide data/support to study Investigators, sponsors and/or external monitors/auditors
- Direct the activities of research support staff. Assist with the training of staff
- Develop preliminary designs for study related documentation of data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)
- Contribute to grant preparation, assessment of protocol feasibility, manuscript writing, data presentations and Institutional Review Board (IRB) processes
Duties Noted Above Plus:- Responsible for internal review/monitoring of clinical data for quality assurance purposes. Reports findings
- Responsible for the smooth operation of all assigned studies on a day-to-day basis, interacting with investigators, staff members, clinicians, sponsors, etc. to ensure project timelines and goals are met
- Contribute independently to the development of preliminary designs for study related documentation of data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)
- May Supervise the activities of research support staff. Assist with the selection, training, and supervision of staff
- Prepare ongoing summary reports from various data sources, and collaborate with investigators on data presentation, interpretation, and the writing of manuscripts for publication and grant proposals
- Identify and resolve issues with protocol compliance. Keep principal investigator and manager aware of any issues regarding compliance
- Accountable for quality assurance reviews of study data
- Assist with financial /operational aspects of grant and contracts. Responsible for clinical research billing review within the required timeframe.
- Contribute independently to grant preparation, assessment of protocol feasibility, manuscript writing, data presentations and Institutional Review Board (IRB) processes
Clinical Research Coord I:- Bachelors degree in a scientific or health related field, or equivalent experience
- 0-1 year of related experience
- Ability to travel off site locations
- Requirements noted for CRC I plus:
- 1-3 years of related experience
- Requirements noted for CRC I plus:
- 3-5 years of related experience
- Requirements noted for CRC I plus:
- 5-7 years of related experience
- Demonstrated knowledge of quality management principles in a scientific or hospital setting
As an equal opportunity and affirmative action employer, UMass Chan recognizes the power of a diverse community and encourages applications from individuals with varied experiences, perspectives and backgrounds. - 9 Days Ago
Clinical Research Coordinator - Open Rank
- UMass Med School
-
Lincoln, RI
FULL_TIME
- Clinical Research Coordinator - Open Rank Minimum Salary US-RI-Lincoln Job Location 7 hours ago(2/26/2024 6:51 AM) Requisition Number 2024-45550 # of Openings 1 Posted Date Day Shift Exempt Exempt/Non...
- 12 Days Ago
Clinical Research Coordinator - Open Rank
- University of Massachusetts Medical School
-
Lincoln, RI
OTHER
- Overview POSITION SUMMARY: Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator is responsible for independently performing delegated tasks and procedu...
- 2 Months Ago
Principal Investigator
- Velocity Clinical Research, Inc.
-
East Greenwich, RI
FULL_TIME
- Overview Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we ...
- 30 Days Ago
FOREIGN TRAVEL COORDINATOR - GM
- McLaughlin Research Corp
-
Newport, RI
FULL_TIME
- Job Description: McLaughlin Research Corporation (MRC) has an immediate opening for a Foreign Travel Coordinator in support of NUWC Division Newport. The qualified candidate will be responsible for An...
- 23 Days Ago
Clinical Research Assistant - RI
- Panoramic Health
-
Providence, RI
FULL_TIME
- The Clinical Research Assistant is responsible for providing support to the clinical research coordinators (CRCs) through direct and administrative involvement in the conduct of research within a PH c...
- Just Posted
Clinical Research Coordinator jobs at Popular Companies
About Rhode Island
Rhode Island (/ˌroʊd -/ (listen)), officially the State of Rhode Island and Providence Plantations, is a state in the New England region of the United States. It is the smallest state in area, the seventh least populous, the second most densely populated, and it has the longest official name of any state. Rhode Island is bordered by Connecticut to the west, Massachusetts to the north and east, and the Atlantic Ocean to the south via Rhode Island Sound and Block Island Sound. It also shares a small maritime border with New York. Providence is the state capital and most populous city in Rhode Is...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Coordinator jobs
$63,002 to $84,949
Most Popular Cities in Rhode Island for Clinical Research Coordinator Jobs
What does a Clinical Research Coordinator do?
Clinical Research Coordinator in Rock Hill, SC
A clinical research coordinator coordinates the clinical trials under the guidance of the principal investigator.
October 22, 2019
Clinical Research Coordinator in Binghamton, NY
However, many people start working in research with no experience and can receive on-the-job training and experience.
November 18, 2019
Clinical Research Coordinator in Portsmouth, NH
With an experienced coordinator, just as with an inexperienced one, it’s the same.
December 11, 2019