Clinical Trials Data Coordinator & Study Support

Indiana University; Indianapolis (IN); On-site; USD 55,000 - 85,000; Full time

Benefits offered by this job

Medical and dental insurance

Health savings account (HSA)

Tuition subsidy

Paid holidays & time off

Retirement benefits

Employee assistance program

Job summary

Indiana University in Indianapolis seeks a Clinical Research Support role within the IUSCCC CTO to aid conduct of adult and pediatric trials. The position supports protocol development, data collection, and regulatory documentation in a fast-paced research environment.

The role involves coordinating study activities, assisting with recruitment and consent, and ensuring quality documentation for audits and sponsor requirements. A relevant degree and experience are preferred.

Qualifications

• Proficient written and verbal communication skills.
• Maintains a high degree of professionalism.
• Demonstrates time management and priority setting skills.
• Demonstrates a high commitment to quality.
• Possesses flexibility to work in a fast paced, dynamic environment.
• Highly thorough and dependable.

Responsibilities

• Assists in the conduct of clinical research studies or trials following established protocols and SOPs.
• Assists with identifying and recruiting subjects for clinical research studies or trials; calls/schedules subjects for appointments per protocol; performs screening, consenting and interviewing/data collection in adherence with the assigned study protocol and in accordance with good clinical principles; collects patient consent and authorization for treatment intervention documents and performs those interventions as needed.
• Conducts routine experiments and/or coordinates research study procedures in accordance with SOPs; records study data; keeps researchers/PI up-to-date on problems related to the study; may collect clinical samples for research.
• Assists with advertising and other information for participant recruitment; develops and shares educational resources with subjects and families.
• Ensures proper documentation of Case Report Forms, regulatory documents, PI notes, and other mandatory study documents; archives per sponsor/government requirements; maintains records for audits.
• Maintains and manages inventory and research supplies; may facilitate disbursement of participant payments.
• Provides additional research support such as literature reviews, grant preparation, manuscript review/editing, and literature searches.

Education

Bachelor's degree in science or a health-related field

Associate’s degree in an allied health profession

High school diploma or equivalent with 5 years of patient-related or research experience

Tools

Proficient written and verbal communication skills

Job description

Indiana University in Indianapolis seeks a Clinical Research Support role within the IUSCCC CTO to aid conduct of adult and pediatric trials. The position supports protocol development, data collection, and regulatory documentation in a fast-paced research environment.

The role involves coordinating study activities, assisting with recruitment and consent, and ensuring quality documentation for audits and sponsor requirements. A relevant degree and experience are preferred.