Coord,Clinical Research I
Company: UMass Med School
Location: Worcester
Posted on: March 16, 2023
Job Description:
Coord,Clinical Research I
Minimum Salary
US-MA-Worcester
Job Location
3 days ago(3/10/2023 10:56 AM)
Requisition Number
2020-35866
# of Openings
1
Posted Date
Day
Shift
Exempt
Exempt/Non-Exempt Status
Non Union Position -W60- Non Unit Professional
Overview
POSITION SUMMARY:Under the direction of the Principal Investigator
(PI) or designee, the Clinical Research Coordinator I 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.
Responsibilities
ESSENTIAL FUNCTIONS:
Obtain consent of research
participants in accordance with the IRB approved protocols and all
applicable regulations including HIPAAIdentify, schedule and/or
conduct participant study visits, interviews, and testsCoordinate
participant remuneration/compensation per protocolMaintain all
regulatory documentation, including local or central IRB and study
data. Provide data/support to study Investigators, sponsors and/or
external monitors/auditorsIdentify issues with protocol compliance.
Keep principal investigator and manager aware of any issues
regarding complianceDocument 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 protocolTrack and maintain study enrollment
and completion of milestonesAssist 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 timeframeResponsible for monitoring the
inventory of research related suppliesParticipate in grant
preparation, manuscript writing, data presentations and
Institutional Review Board (IRB) processesProvide detailed written
summaries from literature searches and related sources to serve as
a resource for the study team and clinicians/PIsPresent study
status reports related to assigned research projectsParticipate 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
positionAdhere with established policies, health and safety
regulations and requirements, procedures, and department
objectivesAdhere to Good Clinical Practice (GCP) guidelines and all
human subject protection practicesMust practice discretion and
adhere
Qualifications
REQUIRED QUALIFICATIONS:
Bachelor's degree in a scientific or
health related field, or equivalent experience0-1 year of related
experienceAbility to travel off site locations SUPERVISION
RECEIVED: Under the direction of the Principle Investigator or
designee SUPERVISION EXERCISED: None ENVIRONMENTAL WORKING
CONDITIONS:Usual office environment, laboratory, medical, surgical,
and off campus study sites
Keywords: UMass Med School, Worcester , Coord,Clinical Research I, Healthcare , Worcester, Massachusetts
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