Neurology Clinical Research Coordinator

Socket.dev; Knoxville (TN); On-site; USD 55,000 - 75,000; Full time

Job summary

Socket.dev is seeking a Clinical Research Coordinator (Neurology) to coordinate clinical studies under the direction of the Research Manager, Medical Director, and Principal Investigator. You will handle IRB submissions, consent processes, data entry, and regulatory compliance while coordinating patient care for memory disorders.

Responsibilities include screening and enrollment, protocol adherence, and collaboration with physicians, monitors, and sponsors to ensure high-quality trial conduct.

Qualifications

• Bachelor’s of Science degree from an accredited college or university (nursing degree accepted but not required).
• Experience with GCP and regulatory requirements.
• Experience administering and rating Cognitive Scales/Assessments.
• Perform venipuncture and ECGs.
• Processing laboratory and pathology samples as required per study protocol.

Responsibilities

• Participate in the implementation and management of clinical trials including IRB submissions and patient screening.
• Ensure adherence to SOPs, good clinical practice, and FDA regulations.
• Record data on case report forms according to protocol/sponsor requirements.
• Plan and implement pre-study activities and timelines for trials.
• Recruit, enroll, and follow-up with patients in assigned trials.
• Develop systems to meet accrual goals and resolve protocol queries.

Skills

Cognitive assessments

GCP compliance

Data management

Interpersonal skills

Attention to detail

Education

Bachelor’s of Science degree

Nursing degree accepted

Tools

Microsoft Excel

Microsoft Word

PowerPoint

Data management software

Job description

Socket.dev is seeking a Clinical Research Coordinator (Neurology) to coordinate clinical studies under the direction of the Research Manager, Medical Director, and Principal Investigator. You will handle IRB submissions, consent processes, data entry, and regulatory compliance while coordinating patient care for memory disorders.

Responsibilities include screening and enrollment, protocol adherence, and collaboration with physicians, monitors, and sponsors to ensure high-quality trial conduct.