Search for Jobs

16 Results
UMass Chan Medical School
Worcester, Massachusetts, United States
8 days ago
UMass Chan Medical School
Worcester, Massachusetts, United States
8 days ago
UMass Chan Medical School
Worcester, Massachusetts, United States
8 days ago
UMass Chan Medical School
Worcester, Massachusetts, United States
9 days ago
UMass Chan Medical School
Worcester, Massachusetts, United States
9 days ago
UMass Chan Medical School
Worcester, Massachusetts, United States
9 days ago
Alnylam Pharmaceuticals
Cambridge, Massachusetts, United States
10 days ago
Alnylam Pharmaceuticals
Cambridge, Massachusetts, United States
10 days ago
Alnylam Pharmaceuticals
Cambridge, Massachusetts, United States
10 days ago
Editas Medicine
Massachusetts, United States
13 days ago
Editas Medicine
Massachusetts, United States
13 days ago
Alira Health
Framingham, Massachusetts, United States
13 days ago
UMass Chan Medical School
Worcester, Massachusetts, United States
17 days ago
stratacuity
Boston, Massachusetts, United States
22 days ago
Joslin Diabetes Center
Boston, Massachusetts, United States
22 days ago
Boston Children's Hospital
Boston, MA, United States
30 days ago
1 - 16 Results of 16
UMass Chan Medical School
Worcester, Massachusetts, United States
8 days ago

Description


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 HIPAA
  • Identify, schedule and/or conduct participant study visits, interviews, and tests
  • 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.


Qualifications

REQUIRED QUALIFICATIONS:

  • Bachelor's degree in a scientific or health related field, or equivalent experience
  • 0-1 year of related experience
  • Ability to travel off site locations

Apply Here: https://www.click2apply.net/r7wxpycWBB5qslwfgqX6

PI160645159



Job Information

  • Job ID: 60917357
  • Location:
    Worcester, Massachusetts, United States
  • Position Title: Clinical Research Coordinator I
  • Company Name: UMass Chan Medical School
  • Job Function: Research
  • Job Type: Full-Time
Jobs You May Like
Filters
Job Function
Industry
State