Clinical Research Specialist

Indiana University Indianapolis; Indianapolis (IN); On-site; USD 40,000 - 65,000; Full time

Job summary

An established institution is seeking a dedicated Research Coordinator to assist in recruiting and managing research study subjects. This role involves coordinating study procedures, monitoring compliance, and ensuring data integrity. With a focus on professionalism and effective communication, the ideal candidate will thrive in a dynamic environment while contributing to impactful research initiatives. The position offers a chance to grow within a supportive team while making a meaningful difference in the field of health and science. Comprehensive benefits and opportunities for development are included, making this a rewarding career choice.

Benefits

Comprehensive health insurance

Retirement plans

Tuition subsidies

Paid holidays

Qualifications

• Bachelor's degree in science or health-related field with 1 year experience.
• Associate's degree in allied health with 3 years experience.

Responsibilities

• Assists with identifying and recruiting potential research study subjects.
• Records study data, samples, and results in databases.
• Monitors study team compliance with protocols and SOPs.

Skills

Proficient communication

Professionalism

Time management

Quality focus

Flexibility

Dependability

Initiative

Customer relationship building

Education

Bachelor's degree in science or health-related field

Associate's degree in allied health

Job description

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Job Responsibilities

1. Assists with identifying and recruiting potential research study subjects; determines eligibility according to the IRB/protocol approved methodologies, coordinates study procedures, and monitors the progress of research studies or projects.
2. Conducts study visit activities and coordinates screening, consenting, and scheduling of tests, exams, and assessments involving study subjects; manages follow-up activities based on protocols.
3. Records study data, samples, and results in databases; maintains and validates data; produces reports for study stakeholders.
4. Monitors study team compliance with protocols and SOPs; submits regulatory paperwork; communicates with PIs and investigators about protocol concerns or changes.
5. Assists in developing communication strategies for recruitment and participant information materials.
6. Stays current on regulatory affairs and research best practices through continuing education.
7. Provides additional support such as budget assistance, invoicing, billing compliance, and patient billing resolution.
8. May support or guide less experienced staff.

Qualifications

Education / Work Experience:

• Bachelor's degree in science or health-related field with 1 year experience OR
• Associate's degree in allied health with 3 years experience

Skills:

• Proficient communication
• Professionalism
• Time management
• Quality focus
• Flexibility
• Dependability
• Initiative
• Customer relationship building

Additional Information

The role involves physical activity, including moving objects weighing up to 25 pounds and working near mechanical parts. Accommodations will be provided if needed.

Location

Indianapolis, Indiana

Benefits

Comprehensive health insurance, retirement plans, tuition subsidies, paid holidays, and more.

Application Details

Apply within 5 business days for full consideration. Include a cover letter if desired.

Equal Opportunity Employer

Indiana University is an equal opportunity employer and provider of ADA services.