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Indiana University in Indianapolis is seeking a Clinical Research Technician to support day-to-day studies within the pediatric unit, ensuring activities align with protocols, SOPs, and regulatory requirements.
The role involves identifying and recruiting participants, coordinating visits and procedures, obtaining consent, collecting and documenting study data and clinical samples, and maintaining up-to-date regulatory and study records.
The Department of Pediatrics employs nearly 1,000 faculty and staff who work alongside employees of Riley Hospital for Children and students of Indiana University School of Medicine (IUSM) to make Riley Children's Health Indiana's largest and most skilled pediatric system.
At IUSM, our mission and core values define who we are, how we act, and what we aspire to accomplish.
The Clinical Research Tech supports the day-to-day conduct of clinical research studies within the unit, ensuring study activities are completed in accordance with established protocols, standard operating procedures, and regulatory requirements.
Primary responsibilities include identifying and recruiting participants, coordinating study visits and procedures, conducting screening and consenting activities, collecting and accurately documenting study data and clinical samples.
Conducts research procedures, collects clinical samples as applicable, and accurately collect, enter, and maintain study data in accordance with protocols and SOPs.
Identifies, recruits, screens, consents, and schedules research participants while coordinating study visits and protocol-required procedures.
Maintains accurate case report forms, regulatory documents, PI notes, and other required study records to support quality, compliance, and regulatory audits.
Assists in the conduct of clinical research studies or trials following established protocols and standard operating procedures.
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 principals; 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; receives, collects, and records study data in database; communicates and keeps researchers and/or PI up-to-date on any problems or concerns related to the research study or trial; may be responsible for collecting clinical samples (such as blood, sample tissue, etc.) for research including any storage measures.
Assists with advertising and other information for participant recruitment; assists in developing and sharing educational and informational resources with subjects and families.
Ensures proper documentation of Case Report Forms, regulatory documents, PI notes, and any other mandatory study-related documents and ensures quality and accuracy; archives documents for study per sponsor, government and institutional requirements; keeps accurate records and provides necessary documents for regulatory audits.
Maintains and manages inventory and research study supplies; may be responsible for facilitating disbursement of study participant payments.
Provides various additional research study support (such as protocol research in medical library/online databases, summarizing literature reviews for study hypothesis, grant preparation, manuscript review/editing, literature searches, and/or transcription).
Stays up-to-date on regulatory affairs and/or clinical research best practices by attending continuing education classes, conferences, seminars, and project team meetings.
Combinations of related education and experience may be considered. Education beyond the minimum required may be substituted for work experience. Work experience beyond the minimum required may be substituted for education.
Required
High school diploma or equivalent (such as HSED or GED) plus 5 years patient-related or research experience that includes 2 years of experience with clinical studies; ORAssociate's degree in allied health profession plus 1 year of patient-related or research experience.; ORBachelor's degree in any field or 3 years of college-level science plus 2 years of patient-related or research experience; ORBachelor's degree in science or health-related field
Required
The role regularly requires the ability to effectively communicate. The role frequently requires the ability to move about the work environment and to position oneself to operate laboratory equipment effectively. The role requires the ability to move objects weighing up to 25 pounds and will occasionally work near moving mechanical parts. The person in this role must be able to perform the essential functions with or without an accommodation.
Indianapolis, IndianaAdvertised Salary $40,000.00 - 45,000.00 annually (determined by education, experience, knowledge, skills, and abilities, as required by the role, as well as internal equity and alignment with market data)
For full-time staff employees, Indiana University offers a wide array of benefits including:
Career Level: IntermediateFLSA: NonexemptJob Function: ResearchJob Family: Clinical Research
Indiana University is an equal opportunity employer and provider of ADA services and prohibits discrimination in hiring. See Indiana University Notice of Non-Discrimination here which includes contact information
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