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Research Study Coordinator Jobs in Indiana (NOW HIRING)

ObjectiveHealth

Clinical Research Coordinator I

South Bend, IN · On-site

$23.75 - $31.50/hr

Clinical Research Coordinator I Our clinical research company is looking to hire a qualified ... Taking ownership of assigned studies and patients * Communicating promptly and effectively with ...

Indiana University

Research Analyst

Indianapolis, IN · On-site

$50K - $60K/yr

... basic research in genetic and genomic mechanisms, translational research in disease models, and ... Monitors study timelines. * Coordinates with internal groups to ensure samples move smoothly ...

Ivy Tech

Work Study - ON CAMPUS

Bloomington, IN · On-site

Work in a range of settings including academic departments, research labs, and student services ... Questions specific to Title IX may be referred to the College's Title IX Coordinator or to the US ...

Ivy Tech

Work Study - ON CAMPUS

Bloomington, IN · On-site

Work in a range of settings including academic departments, research labs, and student services ... Questions specific to Title IX may be referred to the College's Title IX Coordinator or to the US ...

Ivy Tech

Work Study - ON CAMPUS

Goshen, IN · On-site

$15/hr

Work in a range of settings including academic departments, research labs, and student services ... Questions specific to Title IX may be referred to the College's Title IX Coordinator or to the US ...

Ivy Tech

Work Study - ON CAMPUS

South Bend, IN · On-site

$15/hr

Work in a range of settings including academic departments, research labs, and student services ... Questions specific to Title IX may be referred to the College's Title IX Coordinator or to the US ...

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All JobsResearch Study JobsResearch Study Coordinator JobsResearch Study Coordinator Jobs in Indiana

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 job categories do people searching Research Study Coordinator jobs in Indiana look for?

The top searched job categories for Research Study Coordinator jobs in Indiana are:

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

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

Research Study Coordinator jobs near you
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.

Clinical Research Coordinator I

ObjectiveHealth

South Bend, IN

$23.75 - $31.50/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 10 days ago

Job description

Description

Clinical Research Coordinator I

Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator. The ideal candidate will possess certification such as an MA, phlebotomy, or similar and have a strong desire to work directly with patients.


Who We Are

ObjectiveHealth is a clinical research company that uses proprietary technology to:

  1. Increase patient access to research trials within our communities,
  2. Provide physicians with enhanced care options for current patients, and
  3. Deliver superior clinical research enrollment metrics to Pharma sponsors

All with the goal of Improving Patient Outcomes at the Point of Care. We want you to join us in doing just that.


Who You Are

  • A lover of patient interaction and skilled at providing patient care
  • A team player with a bias for action and an attitude that takes personal responsibility
  • Skilled in all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc.
  • Skilled at performing and assisting with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG, etc.
  • Possess an acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set-up and maintenance, and strict protocol adherence
  • An expert communicator with the goal of fostering relationships between the research team, PIs, Sponsors, Monitors, and others
  • A strong advocate for Company values, mission, and initiatives
  • Not easily distracted: You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies
  • Energized by the idea of playing a role in the future of new therapy development in the areas of Gastroenterology, Urology, Dermatology, and/or Oncology


What Success Looks Like for This Role

  • Taking ownership of assigned studies and patients
  • Communicating promptly and effectively with leadership and coworkers when you have a question or see something that needs correction
  • Showing up on time, every time
  • Ensuring strict compliance to the laws, regulations, and requirements of all applicable governing bodies
  • Learning and using the technologies we provide to increase efficiency in your day-to-day activities
  • Embodying our core values of Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication


What We Offer

Competitive compensation, 401(k) with Company match, a clear career pathway for advancement within the Company, Short- and Long-Term Disability, Health Savings and Flexible Spending Accounts, Health, Dental and Vision insurance Plans, Generous PTO, Adoption Assistance, Paid Holidays, and a wide selection of other voluntary benefits.

Requirements

This job requires legal authorization to work in the US. We are not currently accepting work visas. ObjectiveHealth is an EEO Employer and an E-Verify participant.

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