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Research Study Coordinator Jobs in Indiana (NOW HIRING)

... researchers, pharmaceutical companies and health systems make confident decisions and improve ... Study Coordinator I - Bioanalytical Work Schedule - Monday - Friday (Day Shift) Job ...

... researchers, pharmaceutical companies and health systems make confident decisions and improve ... Study Coordinator I - Bioanalytical Work Schedule - Monday - Friday (Day Shift) Job ...

Research Contracts Admin

Evansville, IN · On-site

$19.14 - $26.79/hr

You'll work closely with research leadership, investigators, study coordinators, sponsors, Contract Research Organizations (CROs), and finance teams to evaluate new research opportunities, negotiate ...

Is responsible for the coordination and delivery of primary care to BMG research patients entered on clinical research studies. Provides support to the patient (and caregiver) throughout the ...

Is responsible for the coordination and delivery of primary care to BMG research patients entered on clinical research studies. Provides support to the patient (and caregiver) throughout the ...

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Showing results 1-20

Research Study Coordinator information

See Indiana salary details

$20.5K

$76.7K

$107K

How much do research study coordinator jobs pay per year?

As of Aug 14, 2026, the average yearly pay for research study coordinator in Indiana is $76,667.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,000.00 and $94,700.00 per year, depending on experience, location, and employer.

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

AspectResearch Study CoordinatorResearch Assistant
CredentialsBachelor's degree often required; certification optionalTypically requires a bachelor's degree or current student status
Work EnvironmentLeads study activities, manages protocols, interacts with staff and participantsSupports data collection, performs administrative tasks, assists with experiments
Employer & Industry UsageUsed in clinical research, academic, and healthcare settingsCommon in research labs, universities, and clinical trials

The Research Study Coordinator and Research Assistant roles often overlap in credentials and work environments, but coordinators typically have more responsibility in managing study protocols and participant interactions. Both roles are essential in research settings, with coordinators taking a leadership role in study execution.

What is a research study coordinator?

Research Study Coordinators are professionals responsible for managing and overseeing the day-to-day operations of clinical trials or research studies. They ensure that studies are conducted according to protocols, regulatory guidelines, and ethical standards. Their duties often include recruiting and enrolling participants, collecting and managing data, coordinating with research teams, and maintaining accurate documentation. Research Study Coordinators play a crucial role in ensuring the integrity and success of research projects.

What are some typical challenges faced by research study coordinators when managing multiple clinical trials simultaneously?

Research Study Coordinators often juggle several studies at once, which requires exceptional organizational and time-management skills. Common challenges include keeping meticulous records for each trial, ensuring protocol compliance, and coordinating schedules among investigators, sponsors, and participants. Managing regulatory documentation and staying updated with changing study protocols can also be demanding. Successful coordinators proactively communicate with their teams and utilize digital tools to streamline processes, ensuring each study stays on track.

What are the key skills and qualifications needed to thrive as a research study coordinator?

To thrive as a Research Study Coordinator, you need a background in life sciences or health-related fields, experience with research protocols, and often a bachelor's or master's degree. Familiarity with data management systems, regulatory compliance platforms (such as IRB software), and sometimes certifications like CCRC are typically required. Strong organizational abilities, attention to detail, and effective communication help manage study logistics and participant interactions. These skills are important to ensure studies run efficiently, data is accurate, and compliance with ethical and regulatory standards is maintained.

Do research study coordinators need a degree?

Research study coordinators typically need at least a bachelor's degree in a health-related field such as nursing, biology, or psychology. Relevant skills include knowledge of clinical protocols, data management, and regulatory compliance, and some positions may require certification or experience in research methods.

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 are popular job titles related to Research Study Coordinator jobs in Indiana?

For Research Study Coordinator jobs in Indiana, the most frequently searched job titles are:

What cities in Indiana are hiring for Research Study Coordinator jobs?

Cities in Indiana with the most Research Study Coordinator job openings:

Infographic showing various Research Study Coordinator job openings in Indiana as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 85% Full Time, 11% Part Time, and 2% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $76,667 per year, or $36.9 per hour.

Study Coordinator I

Labcorp

Indianapolis, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago


Labcorp rating

6.6

Company rating: 6.6 out of 10

Based on 1,140 frontline employees who took The Breakroom Quiz

97th of 120 rated laboratories


Job description


Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world's most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you'll have the opportunity to do meaningful work, grow your career and make a real impact on people's health around the world. Together, we're improving health and improving lives.


Study Coordinator I - Bioanalytical

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

  • 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

  • Obtains client approval for study finalization

Minimum Qualifications:

  • Bachelors Degree

  • 2 or more years of experience in data analytics position

Preferred Qualifications:

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

  • 3 or more years 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

Position will be posted 8/5 thru 8/10/2026

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

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit ouraccessibility siteor contact us atLabcorp Accessibility. Formore information about how we collect and store your personal data, please see ourPrivacy Statement.



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