Clinical Research Coordinator II
SoundCloud
full-time
Posted on:
Location Type: Office
Location: Worcester • Massachusetts • 🇺🇸 United States
Visit company websiteJob Level
Junior
Tech Stack
Google Cloud Platform
About the role
- 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
- Ensure accuracy and completion of all regulatory documentation, including local or central IRB and study data
- Conduct preliminary quality assurance reviews of study data
- Assist with financial /operational aspects of grant and contracts. May be responsible for clinical research billing review within the required timeframe
- Present study status reports related to assigned research projects
- 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
- Provide detailed written summaries from literature searches and related sources to serve as a resource for the study team and clinicians/PIs
- Contribute to the design, development, and documentation of study related data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)
- Responsible for monitoring the inventory of research related supplies
- 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
- Comply with all safety and infection control standards appropriate to this position
- Adhere to Good Clinical Practice (GCP) guidelines and all human subject protection practices
- Perform other duties as required.
Requirements
- Bachelor’s degree in a scientific or health related field, or equivalent experience
- 1-3 years of related experience
- Ability to travel off site locations
Benefits
- Health insurance
- Professional development
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
data managementquality assuranceregulatory documentationclinical research billingdata collection toolsliterature searchesprotocol complianceGood Clinical Practice (GCP)IRB processesstudy design
Soft skills
communicationorganizationalproblem-solvingattention to detailteam collaborationtime managementadaptabilityreportinginterpersonalmonitoring