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Study Coordinator Jobs in Indiana (NOW HIRING)

Corteva Agriscience

Study Monitor

Indianapolis, IN · On-site

In this role, you will be responsible for coordinating and executing studies at global contract labs that are required for crop protection and biological registrations, both for active ingredients ...

Deaconess

Research Contracts Admin

Evansville, IN · On-site

$19.14 - $26.79/hr

... with Study Coordinator and/or investigator, review to verify and approve all procedures. * Review fee ticket drafts with Coding & Reimbursement Manager, verify the appropriate service codes ...

Iterative Health

Clinical Research Coordinator I

New Albany, IN · On-site

$22.50 - $29.75/hr

Clinical Research Coordinator I Iterative Health is a healthcare technology and services company ... Dispense study medication, collect vital signs and perform ECGs * Perform blood draws, process and ...

Iterative Health

Clinical Research Coordinator I

New Albany, IN · On-site

$22.50 - $29.75/hr

Clinical Research Coordinator I Iterative Health is a healthcare technology and services company ... Dispense study medication, collect vital signs and perform ECGs * Perform blood draws, process and ...

DaVita

$23.50 - $31/hr

Responsible for performing research procedures according to the study protocol and working in ... Certified Clinical Research Coordinator (SOCRA or ACRP) - preferred DaVita Clinical Research (DCR ...

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Study Coordinator information

See Indiana salary details

$20.9K

$52.2K

$76.6K

How much do study coordinator jobs pay per year?

As of Jun 17, 2026, the average yearly pay for study coordinator in Indiana is $52,196.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,900.00 and $59,500.00 per year, depending on experience, location, and employer.

Is CRA higher than CRC?

A Clinical Research Associate (CRA) typically has a higher level of responsibility and seniority than a Clinical Research Coordinator (CRC). CRAs often oversee multiple sites, monitor clinical trials, and ensure compliance with regulations, while CRCs handle day-to-day trial activities at a single site. Advancement from CRC to CRA usually requires additional experience and certifications in clinical research.

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

To thrive as a Study Coordinator, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, usually backed by a bachelor’s degree in a science or health-related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is typically required. Strong organizational skills, attention to detail, and effective communication help you manage study logistics and collaborate with research teams and participants. These skills ensure that studies are conducted ethically, efficiently, and in accordance with regulatory standards.

What jobs pay 2000 a day?

Some high-paying roles for study coordinators or similar positions can reach $2,000 per day, especially in specialized clinical research, consulting, or executive-level roles. These positions often require advanced qualifications, extensive experience, or working in high-stakes environments, and may involve long hours or project-based compensation structures.

Can you be a CRA with no experience?

A Clinical Research Associate (CRA) typically requires prior experience in clinical trials, monitoring, or related roles. Entry-level positions may be available for those with strong organizational skills and relevant education, but most CRAs gain experience through related positions such as study coordinators or research assistants before advancing to a CRA role.

What Is a Study Coordinator?

A study coordinator works in a clinical research environment. In this position, your job duties are to oversee the day-to-day operations of a given study under the guidance of a research director. You direct tests, ensure all research is done according to ethical standards, and ensure the comfort and safety of subjects. As a study coordinator, you also ensure all patients provide informed consent prior to participation. Overall, your responsibility is to provide a safe environment for the study. To be a study coordinator, the qualifications are usually a bachelor’s degree or an RN degree. You typically need several years of experience in a clinical setting, and you must demonstrate skills in research.

What is a Study Coordinator?

A Study Coordinator is a professional responsible for managing and overseeing clinical or research studies, ensuring protocols are followed, data is accurately collected, and regulatory requirements are met. They often work closely with researchers, participants, and institutional review boards, and may require knowledge of Good Clinical Practice (GCP) and data management tools. The role typically involves scheduling, documentation, and compliance tasks to support study integrity.

What are study coordinators?

Study coordinators are professionals who manage the day-to-day operations of clinical research studies. They are responsible for tasks such as recruiting participants, ensuring protocol compliance, collecting and managing data, and maintaining communication between investigators, participants, and regulatory bodies. Study coordinators play a vital role in making sure that research studies are conducted ethically, efficiently, and according to regulatory guidelines. Their work ensures the integrity of study data and the safety of participants throughout the research process.

What are some common challenges Study Coordinators face when managing multiple clinical trials simultaneously?

Study Coordinators often juggle several clinical trials at once, each with its own protocols, timelines, and regulatory requirements. Keeping track of participant enrollment, data collection, and compliance across different studies can be demanding and requires strong organizational skills. Effective communication with investigators, sponsors, and other team members is crucial to prevent errors, ensure deadlines are met, and maintain the quality of study data. Using robust tracking systems and prioritizing tasks can help manage these challenges efficiently.

What is the difference between Study Coordinator vs Research Assistant?

AspectStudy CoordinatorResearch Assistant
Required CredentialsTypically a bachelor's degree in health sciences, biology, or related fieldOften a bachelor's degree or current student in a related field
Work EnvironmentClinical research settings, hospitals, or research institutionsLaboratories, research centers, or clinical sites
Employer & Industry UsageUsed by hospitals, universities, and research organizationsCommonly employed in academic and research institutions
Common Search & Comparison IntentUnderstanding roles, responsibilities, and qualificationsLearning about entry-level research roles and support tasks

The Study Coordinator and Research Assistant roles share similarities in working within research environments and requiring related educational backgrounds. However, Study Coordinators typically have more responsibilities in managing study protocols and participant coordination, while Research Assistants focus on supporting research activities and data collection. Both roles are essential in advancing clinical research and often work closely together in research projects.

More about Study Coordinator jobs
What are the most commonly searched types of Study jobs in Indiana? The most popular types of Study jobs in Indiana are:
What are popular job titles related to Study Coordinator jobs in Indiana? For Study Coordinator jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Study Coordinator jobs in Indiana look for? The top searched job categories for Study Coordinator jobs in Indiana are:
What cities in Indiana are hiring for Study Coordinator jobs? Cities in Indiana with the most Study Coordinator job openings:
Study Coordinator jobs near you
Infographic showing various Study Coordinator job openings in Indiana as of June 2026, with employment types broken down into 93% Full Time, and 7% Part Time. Highlights an 100% In-person job distribution, with an average salary of $52,196 per year, or $25.1 per hour.
Study Coordinator I - Bioanalytical Lab Operations

Study Coordinator I - Bioanalytical Lab Operations

Labcorp

Indianapolis, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago

Labcorp rating

6.6

Company rating: 6.6 out of 10

Based on 1,098 frontline employees who took The Breakroom Quiz

78th of 103 rated laboratories

Job description

Study Coordinator I - Bioanalytics

Work Schedule - Monday - Friday (Day Shift)

Job Responsibilities:

  • Communicates and interacts with clients regarding study progress and reporting activities

  • Review and approve client supplied data transmission specifications

  • Address client comments and queries on data tables and reports

  • Participate in study-related meetings with clients and internal study teams

  • Collaborate with clients regarding report format requirements and transmission processes

  • Collaborate with clients regarding new service requests or changes to reporting scope

  • Learns to serve as the primary contact in communication with clients

  • Represent the Bioanalytical Study Coordination function in client visits, audits, and inspections as needed

  • Learns to support studies for key clients

  • Responsible for study report preparation and completion

  • Creates data tables and is responsible for result reporting to clients

  • Involved with quality review processes of data and reports including Quality Control and Quality Assurance reviews

  • Delivers results and study reports to clients

  • Obtains client approval for study finalization

Minimum Qualifications:

  • Bachelors Degree

  • 3 or more years of experience in data analytics position

Preferred Qualifications:

  • Bachelors Degree in a Science field (e.g. chemistry or biology)

  • 1 year or more experience preparing spreadsheet reports including tables

Additional Job Standards:

  • Use word processing software, database, spreadsheet, and specialized software

  • Excellent communication and interpersonal skills

  • Excellent attention to detail

  • Ability to prioritize, organize, and manage time

Application Window - 6/4 thru 6/10/26

Benefits:

Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan.For more detailed information, pleaseclick here

Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.

We encourage all to apply

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