ZipRecruiter

Log In

1

Research Study Assistant Jobs in Indiana (NOW HIRING)

Inotiv

Research Technician

Evansville, IN · On-site

$23/hr

Support GLP-compliant studies that advance drug development * Participate in reviewing and updating ... and assist during surgical procedures * Monitor anesthetized animals and manage post-op care ...

Inotivco

Research Technician

Evansville, IN · On-site

$23/hr

Support GLP-compliant studies that advance drug development * Participate in reviewing and updating ... and assist during surgical procedures * Monitor anesthetized animals and manage post-op care ...

next page

Showing results 1-20

All JobsResearch Study Assistant JobsResearch Study Assistant Jobs in Indiana

Research Study Assistant information

See Indiana salary details

$8

$20

$30

How much do research study assistant jobs pay per hour?

As of Jul 1, 2026, the average hourly pay for research study assistant in Indiana is $20.85, according to ZipRecruiter salary data. Most workers in this role earn between $17.60 and $24.23 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Research Study Assistant, and why are they important?

To thrive as a Research Study Assistant, you need a solid understanding of research methods, data collection, and basic statistical analysis, often supported by a bachelor's degree in a relevant field. Familiarity with data management software (such as REDCap or SPSS) and compliance with research ethics certifications are typical requirements. Attention to detail, strong organizational abilities, and effective communication skills are vital soft skills for this role. These competencies ensure accurate data handling, adherence to protocols, and successful collaboration with research teams.

What qualifications do I need to be a research assistant?

Research Study Assistants typically need a high school diploma or equivalent; some positions prefer or require a bachelor's degree in a related field. Strong organizational skills, attention to detail, and familiarity with data collection tools or software are also important qualifications for this role.

What is the difference between Research Study Assistant vs Research Coordinator?

AspectResearch Study AssistantResearch Coordinator
CredentialsTypically requires a bachelor's degree in a related fieldOften requires a bachelor's degree; some roles prefer or require additional certifications
Work EnvironmentAssists with data collection, participant recruitment, and administrative tasks in research settingsOversees study protocols, manages staff, and ensures compliance in research projects
Employer & IndustryHospitals, universities, research institutesHospitals, research organizations, academic institutions

The main difference is that Research Study Assistants support data collection and administrative tasks, while Research Coordinators manage study operations and oversee research projects. Both roles are essential in research settings but differ in responsibilities and level of oversight.

What are Research Study Assistants?

Research Study Assistants are professionals who support the design, implementation, and management of research studies, often in academic, medical, or scientific settings. Their responsibilities typically include recruiting participants, collecting and organizing data, maintaining study records, and ensuring compliance with research protocols. They work closely with principal investigators and other research staff to ensure studies run smoothly and efficiently. Research Study Assistants play a crucial role in maintaining data integrity and supporting the overall success of research projects.

How hard is it to get a job as a research assistant?

Securing a research assistant position typically requires relevant educational background, such as a degree in a related field, and strong organizational or data management skills. Competition can vary depending on the institution and field, but having prior research experience or familiarity with tools like statistical software can improve chances.

What are some typical challenges Research Study Assistants face when coordinating participant recruitment and data collection?

Research Study Assistants often encounter challenges such as recruiting enough qualified participants within tight timelines and maintaining participant engagement throughout the study. Managing scheduling conflicts, ensuring informed consent, and adhering to strict data collection protocols are also common hurdles. Successful assistants are proactive in communication, detail-oriented, and adept at troubleshooting unexpected issues that may arise during recruitment or data gathering. Building rapport with participants and collaborating closely with the research team helps address these challenges effectively.

What does a research assistant do?

A research assistant supports data collection, analysis, and organization for research projects. They may conduct experiments, review literature, and prepare reports, often using tools like spreadsheets or statistical software, and typically work under the supervision of a lead researcher.

What is a research study assistant?

A research study assistant is a professional who supports the planning, coordination, and execution of research projects, often handling tasks such as data collection, data entry, and maintaining study documentation. They typically work under the supervision of researchers and may use tools like spreadsheets or specialized software to ensure accurate and efficient data management.
What are the most commonly searched types of Research Study jobs in Indiana? The most popular types of Research Study jobs in Indiana are:
What cities in Indiana are hiring for Research Study Assistant jobs? Cities in Indiana with the most Research Study Assistant job openings:
Research Study Assistant jobs near you

Clinical Research Coordinator II

Iterative Health

New Albany, IN • On-site

$22.50 - $29.75/hr

Full-time

Posted 24 days ago

Job description

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.
We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.
Clinical Research Coordinator II
Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.
We are seeking a full-time, experienced Clinical Research Coordinator - Level II (CRC II). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.
Responsibilities:
  • Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management. Manage a full schedule of complex study visits and corresponding tasks with minimal direction.
  • Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies, with accountability for achieving enrollment goals
  • Schedule all patient research visits and procedures consistent with protocol requirements
  • Conduct patient visits as outlined within each study protocol
  • Dispense study medication, collect vital signs and perform ECGs
  • Perform blood draws, process and ship specimens per study protocol and IATA regulations
  • Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms. Maintain high quality data entry within established timelines
  • Act as point of contact for study participants
  • Adhere to Research SOPs, Good Clinical Practices, and the study protocols
  • Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager, central Iterative Health team, and PI throughout the study. Resolve routine sponsor and CRO issues independently
  • Ensure all safety data is reviewed by the PI in a timely manner
  • Maintain inventory of study equipment and supplies onsite at all times
  • Contribute to status updates to management; contribute and implement ideas to improve site performance
  • Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol. Meet requirements for data query resolution times and quality.
  • Schedule and prepare for monitor visits
  • Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations
  • Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance
  • Complete and maintain case report forms per FDA guidelines, and review them against the patient's medical record for completeness and accuracy

Iterative Health Expectations
All employees are expected to:
  • Perform quality work within deadlines with or without direct supervision
  • Interact professionally with other employees, customers and suppliers
  • Work effectively as a team contributor on all assignments
  • Work independently while understanding the necessity for communicating and coordinating work efforts with other employees and organizations

Qualifications
  • Medical Assistant, LPN, Associates or Bachelor's degree in a clinical or scientific-related discipline preferred
  • Minimum 3 years of clinical research experience
  • Ability to own issues and problem solve independently
  • Experience in phlebotomy preferred
  • Strong written and verbal communication skils
  • Ability to read, interpret, and apply clinic policies and research protocols
  • Ability to use standard office software
  • Must be able to lift up to 25 pounds

At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.
At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.

Apply