Clinical Data Coordinator (Clinical Research Technician)
Company: Indiana University
Location: Indianapolis
Posted on: May 9, 2024
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Job Description:
The mission of the IU Simon Comprehensive Cancer Center (IUSCCC)
Clinical Trials Office (CTO) is to support and facilitate the
conduct of quality clinical research by IUSCCC translational
clinical investigators. The CTO is a centralized resource available
to all clinical investigators of the IUSCCC whose services enable
the safe and efficient conduct of adult and pediatric trials. The
CTO provides a comprehensive range of services. These services
begin in the early stages of protocol development and continue
throughout the study implementation, publication and long-term
follow-up.
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; 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; for research including any storage measures.
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;
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.
Education beyond the minimum required may be substituted for work
experience. Work experience beyond the minimum required may be
substituted for education.
EDUCATION / WORK EXPERIENCE
Bachelor's degree in science or health-related field; Associate's
degree in allied health profession plus 1 year of patient-related
or research experience; Bachelor's degree in any field OR 3 years
of college-level science plus 2 years of patient-related or
research experience; 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.
Demonstrates a high commitment to quality.
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.
IUSCCC Clinical Trials Office
For full-time staff employees, Indiana University offers a wide
array of benefits including:
- Multiple plan options for medical insurance
- Dental insurance
- Health Savings Account with generous IU contribution
- Base retirement plan contribution from IU, subject to vesting
- Additional supplemental retirement plan options
- 10 paid holidays per year
- Employee Assistance Program (EAP)
Learn more about our benefits by reviewing our online Benefits
Brochure.
Research
Clinical Research
To guarantee full consideration, please submit your application
within 5 business days of the Posted Date.
Indiana University prohibits discrimination based on age,
ethnicity, color, race, religion, sex, sexual orientation, gender
identity or expression, genetic information, marital status,
national origin, disability status or protected veteran status.
Questions or complaints regarding Title IX may be referred to the
U.Department of Education Office for Civil Rights or the university
Title IX Coordinator. The Annual Security and Fire Safety Report,
containing policy statements, crime and fire statistics for all
Indiana University campuses, is available online. Telephone:
812-856-1234
Keywords: Indiana University, Lawrence , Clinical Data Coordinator (Clinical Research Technician), Healthcare , Indianapolis, Indiana
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