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Clinical Research Coordinator

2 months ago

Boston, United States SQRL Full time

Highlights:


  • $34.00/Hr. - $36.00/Hr. + Monthly CRC commission that could be up to $2,000.00
  • Full Benefits and Consistent M-F schedule
  • Fast growing company with tons of opportunity


**This is an on-site position in the Roslindale area of Boston, MA. Please do not apply if you are seeking Hybrid or remote**


The Company:


Our client is a growing multi-site, multi-phase clinical research company with a network of locations in Boston and Northern MA, Portsmouth, NH, Charleston, SC, and Detroit, MI. They have established a strong presence across Phase I-IV studies and a variety of therapeutic areas.


The Role:


Responsible for coordinating and overseeing various aspects of clinical research studies, ensuring compliance with protocols and regulatory requirements.


  • Perform patient-facing duties such as screening patients for study enrollment, scheduling study visits, informing patients of consent to partake in trials, doing follow-up visits, and obtaining vital signs and ECGs.
  • Enter data into the EDC and answer queries.
  • May perform basic lab procedures per protocol, such as blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens, and notification of courier for specimen pick-up
  • Request and track medical record requests.
  • Update and maintain logs, and chart filings.
  • Maintain & order study-specific supplies.
  • Conduct monitoring visits and resolve issues as needed in a timely manner.
  • Ensure study-related reports and patient results are reviewed by the investigator in a timely manner.
  • File SAE/Deviation reports to Sponsor and IRB as needed.
  • Document and report adverse events.
  • Complete all needed activities for study start-up, including completing required training, uploading/printing certificates to file in ISF, etc.
  • Prepare and attend site initiation visits (SIVs) and Investigator Meetings (IMs), as needed.


Requirements:


  • 2+ years of Clinical Research experience as a Clinical Research Coordinator
  • Phlebotomy experience