Neuro Clinical Research Coordinator - Academic Trials

Indiana University; Indianapolis (IN); On-site; USD 52,000 - 76,000; Full time

Benefits offered by this job

Comprehensive medical and dental_ins

Health savings account with generousIU

Tuition subsidy for employees and/or家

10 paid holidays + winter break

Generous paid time off

Employee assistance program (EAP)

Job summary

Indiana University in Indiana is seeking a Clinical Research professional for the Neurology department. The role focuses on protocol design, regulatory compliance, and subject recruitment within a busy academic research setting.

Responsibilities include budgeting, IRB submissions, subject screening, data collection, and coordination with healthcare teams. Strong organizational skills and attention to quality are essential for success.

Qualifications

• Bachelor's degree plus 1 year clinical research experience, OR Associate's degree plus 3 years clinical research experience.
• SOCRA/ACRP certification preferred at date of hire.

Responsibilities

• Initiates and conducts protocol review, evaluations, study design, and risk assessments.
• Participates in study budget negotiations and reconciles budget accounts.
• Develops recruitment materials and monitors enrollment goals.
• Ensures regulatory compliance and submits IRB documents and regulatory paperwork.
• Identifies and screens potential subjects and conducts interviews.
• Follows up with stakeholders and manages study documentation.
• Reviews SAE information and assists PI with submission determinations.
• Performs non-medical/behavioral assessments and required procedures.
• Records protocol deviations and stays current with regulatory affairs.

Skills

Analytical skills

Multitasking

Technical aptitude

Quality focus

Organizational skills

Education

Bachelor's degree in science or health-related field

Associate's degree in science or health-related field

Job description

Indiana University in Indiana is seeking a Clinical Research professional for the Neurology department. The role focuses on protocol design, regulatory compliance, and subject recruitment within a busy academic research setting.

Responsibilities include budgeting, IRB submissions, subject screening, data collection, and coordination with healthcare teams. Strong organizational skills and attention to quality are essential for success.