Clinical Research Coordinator 2 - Medical Center

Rolfes Lab

Washington, DC, US
On-campus
Manage and coordinate clinical studies
Conduct study visits according to protocol
Maintain patient confidentiality
The Clinical Research Coordinator 2 (CRC2) position at Rolfes Lab involves managing and coordinating clinical studies focused on Neuromuscular Disorders (ALS) at Georgetown University. Candidates should possess significant experience in clinical trials, particularly in patient interactions and regulatory compliance, and will benefit from a supportive, mission-driven environment. ###

Job Summary

  • The Clinical Research Coordinator 2 is responsible for managing and coordinating the ALL ALS studies, primarily in the disease states of Neuromuscular Disorders (ALS).
  • The CRC2 must maintain a comprehensive functional knowledge of ancillary departments to be involved in trial visits and must be able to communicate and coordinate with such departments effectively.
  • As an employee of Georgetown University, the CRC2 directly supports the University’s mission of cura personalis.

Matching Summary

Match Score: 85

The Clinical Research Coordinator 2 (CRC2) position at Rolfes Lab involves managing and coordinating clinical studies focused on Neuromuscular Disorders (ALS) at Georgetown University. Candidates should possess significant experience in clinical trials, particularly in patient interactions and regulatory compliance, and will benefit from a supportive, mission-driven environment. ###

Skills & Requirements

Must-have

  • Manage and coordinate clinical studies
  • Conduct study visits according to protocol
  • Maintain patient confidentiality
  • Accurate data entry and reporting
  • Communicate with patients and sponsors

Nice-to-have

  • Experience with central IRB protocols
  • Ability to operate a centrifuge
  • Phlebotomy experience

Key Requirements

  • Bachelor's degree minimum
  • 5 years minimum work experience as Clinical Trial Coordinator or Clinical Research Assistant
  • 3 years experience in clinical setting with direct patient interaction
  • 2 years experience as Clinical Trial Coordinator, Clinical Research Assistant, or equivalent
  • Experience working with Neurology patients (MS and neuromuscular clinics)
  • Experience with regulatory maintenance and IRB submissions
  • Current CITI Group 1 Biomedical, HIPAA, and IATA Training
  • Experience handling human biological specimens
  • Experience accessing and reading patient medical records
  • Experience measuring vital signs and obtaining medical histories

Work Rights

Not specified

Tailored Resume

Cover Letter