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Research Study Coordinator Jobs in Indiana (NOW HIRING)

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 ...

$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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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 Sep 5, 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 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 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.

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 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 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, 81% Full Time, 13% Part Time, 1% Temporary, and 3% Contract. Highlights an 83% Physical, 5% Hybrid, and 12% Remote job distribution, with an average salary of $76,667 per year, or $36.9 per hour.

Regional Study Coordinator - Central Labs Services - Clinical Research

Labcorp

Indianapolis, IN • Hybrid

$23.25 - $30.75/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 9 days ago


Key responsibilities

  • Serve as the regional liaison between the Global Study Manager and all CLS departments involved in study execution.

  • Oversee day-to-day local study activities, including logistics, monitoring, and study supplies, and communicate key developments to the Global Study Manager.

  • Monitor, track, and resolve local study issues while supporting proactive issue management and coordination with internal and external stakeholders.


Labcorp rating

6.6

Company rating: 6.6 out of 10

Based on 1,160 frontline employees who took The Breakroom Quiz

95th of 121 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.


Labcorp is seeking a hybrid Regional Study Coordinator to join our Central Labs Services team in Indianapolis.

Job Responsibilities

Serve as the regional liaison between the Global Study Manager and all CLS departments involved in study execution

Act as the regional point of contact for assigned client representatives (e.g., CRAs, Site Monitors) and the corresponding local CLS platform; may occasionally represent the Global Study Manager in interactions with primary client contacts

Partner closely with the Global Study Manager across all study stages-from startup through closure-to ensure seamless coordination of activities within the local platform

Review the Statement of Work (SOW) to assess local feasibility and provide informed recommendations to the Study Design Lead

Maintain deep knowledge of SOW specifications and a strong understanding of how those requirements impact operational delivery across the clinical trial

Oversee daytoday local study activities, including logistics, monitoring, and study supplies, ensuring the Global Study Manager is kept informed of key developments

Monitor, track, and resolve local study issues, maintaining consistent communication with the Global Study Manager to support proactive issue management

The Regional Study Coordinator is expected to interact internally on a regular basis and occasionally with external clients throughout all job duties mentioned above.

Minimum Qualifications

High school diploma or equivalent

Two or more years of professional experience in a clinical research or laboratory setting

Preferred Qualifications

Bachelor's degree in life science discipline

Additional Job Standards

Proven ability to plan, prioritize, and manage workload in fastpaced, deadlinedriven environments

Strong communication and organizational skills that support clear, consistent execution

Exceptional attention to detail paired with a collaborative, teamoriented approach

Demonstrated experience facilitating meetings and engaging effectively with clients to drive alignment and outcomes

Selfstarting, investigative mindset with the ability to learn quickly and adapt in dynamic environments

At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations.

Central Laboratory Services is part of a global contract research organization within Labcorp. We offer the world's largest network of central laboratories and support global clinical trials testing. A common set of processes, procedures, and instrumentation is offered throughout our sites in Europe, Asia/Pacific, and the United States, allowing us to receive samples globally and provide more than 700 assays across all laboratory science disciplines.

Application Window: Closes at the end of the day September 4, 2026.

Pay Range: 60-65K

All job offers will bebased on a candidate's skills and prior relevant experience, applicabledegrees/certifications,as well as internal equity and market data.

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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