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Clinical Research Operations Jobs in Indiana (NOW HIRING)

MediSphere Medical Research Center, LLC

Be Seen First

Clinical Research Assistant II

Evansville, IN · On-site

Maintain study supply inventory. * Assist with general office and clinical operations. Other Related Duties * Cross-train in additional Clinical Research Coordinator responsibilities as assigned.

Actalent

Clinical Research Coordinator

Indianapolis, IN

$21.25 - $28.25/hr

Job Title: Clinical Research Coordinator - Oncology The Clinical Research Coordinator will ... Experience in oncology research and familiarity with cancer center operations. * Demonstrated ...

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Clinical Research Operations information

See Indiana salary details

$46.6K

$102.1K

$179.8K

How much do clinical research operations jobs pay per year?

As of Aug 23, 2026, the average yearly pay for clinical research operations in Indiana is $102,137.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,100.00 and $116,600.00 per year, depending on experience, location, and employer.

What is clinical research operations?

Clinical research operations refer to the planning, execution, and management of clinical trials and studies that test new medical treatments, drugs, or devices. This field ensures that studies are conducted ethically, efficiently, and in compliance with regulatory guidelines. Professionals in clinical research operations coordinate activities such as patient recruitment, data collection, regulatory submissions, and quality control. Their work is essential for advancing medical knowledge and ensuring the safety and effectiveness of new healthcare interventions.

What are the key skills and qualifications needed to thrive in clinical research operations?

To thrive in Clinical Research Operations, you need a strong understanding of clinical trial protocols, regulatory guidelines (such as ICH-GCP), and project management, typically supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are often required. Exceptional organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating teams and ensuring compliance. These competencies are vital for maintaining data integrity, meeting regulatory standards, and successfully managing complex clinical studies.

What are some common challenges faced in clinical research operations and how can they be addressed?

Professionals in clinical research operations often encounter challenges such as managing complex regulatory requirements, coordinating across multidisciplinary teams, and ensuring adherence to strict timelines. Successfully addressing these challenges typically involves strong project management skills, effective communication with stakeholders, and staying updated on regulatory changes. Leveraging technology for data management and fostering a collaborative work environment can also help streamline processes and improve trial outcomes.

What is the difference between Clinical Research Operations vs Clinical Research Coordinators?

AspectClinical Research OperationsClinical Research Coordinators
CredentialsTypically requires a degree in life sciences, certifications like CCRP or RACOften requires a bachelor's degree in health sciences or related field, with certifications like CCRP beneficial
Work EnvironmentOversees multiple studies, manages teams, and collaborates with sponsors and regulatory bodiesWorks directly with study participants, manages data collection, and ensures protocol adherence
Employer & Industry UsageUsed in pharmaceutical companies, CROs, and research institutionsCommonly employed in hospitals, clinics, and research sites

Clinical Research Operations professionals focus on managing entire research programs, budgets, and teams, while Clinical Research Coordinators handle day-to-day study activities and participant interactions. Both roles are essential but differ in scope and responsibilities within the clinical research field.

Is clinical research operations a good career?

Clinical research operations involves managing and coordinating clinical trials to ensure they meet regulatory standards and are completed efficiently. It offers opportunities for growth, requires strong organizational and communication skills, and often involves working with cross-functional teams and specialized software. Many professionals find it a rewarding field with stable employment prospects in the healthcare and pharmaceutical industries.

What are the most commonly searched types of Clinical Research Operations jobs in Indiana?

The most popular types of Clinical Research Operations jobs in Indiana are:

What are popular job titles related to Clinical Research Operations jobs in Indiana?

For Clinical Research Operations jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Clinical Research Operations jobs in Indiana look for?

The top searched job categories for Clinical Research Operations jobs in Indiana are:

What cities in Indiana are hiring for Clinical Research Operations jobs?

Cities in Indiana with the most Clinical Research Operations job openings:

Clinical Research Operations jobs near you
Infographic showing various Clinical Research Operations job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $102,137 per year, or $49.1 per hour.

Mobile Clinical Research Operations Associate

Medasource

Greenwood, IN • On-site

Other

Posted 2 days ago

New

Job description

Job Title: Mobile Research Community Engagement Operations Associate

Contract Length: 18-months

Home Location: Greenwood, IN - Travel Required 2 times per month!

Hours: 8a-5p

Start Date: ASAP


Job Description:

The MRU Operations Associate supports the successful execution of Mobile Research Community Events (MRCEs) by managing on-site logistics, operational setup, and research supply coordination. This role is responsible for ensuring Mobile Research Unit (MRU) readiness, maintaining clinical trial materials and equipment, and supporting compliant, efficient research operations at deployment sites. The ideal candidate is highly organized, adaptable, and comfortable working in a fast-paced, event-based environment while collaborating with cross-functional clinical and operational teams.


Key Responsibilities

  • Support the execution of Mobile Research Community Events (MRCEs) as part of the MRU Operations team.
  • Coordinate on-site event setup, operational activities, and teardown to ensure efficient and compliant event execution.
  • Manage inventory, storage, and transportation of clinical trial materials and operational supplies.
  • Prepare, set up, maintain, and troubleshoot MRU equipment at the Global Innovation Center (GIC) and research event locations.
  • Partner with local clinical teams and internal stakeholders to ensure seamless operational support while adhering to defined MRU deployment responsibilities.
  • Ensure research sites are organized, operationally ready, and compliant with applicable SOPs and operational standards.
  • Represent Lilly professionally at community research events while fostering effective communication with clinical teams, research staff, and event stakeholders.
  • Identify operational issues and escalate or resolve them to minimize disruption to research activities.
  • Support continuous improvement initiatives to enhance MRU operational processes and event execution.

Qualifications

Required:

  • Bachelor's degree or equivalent combination of education and relevant experience.
  • Experience supporting logistics, operations, event coordination, healthcare, research, or clinical environments.
  • Strong organizational skills with the ability to manage multiple priorities in a dynamic environment.
  • Excellent communication and interpersonal skills.
  • Proficiency with Microsoft Office Suite.
  • Willingness to travel extensively and work flexible hours, including occasional evenings and weekends.

Preferred:

  • Experience supporting clinical research, healthcare operations, or mobile healthcare initiatives.
  • Familiarity with inventory management and equipment coordination.
  • Experience working in regulated environments (clinical, healthcare, or life sciences).
  • Knowledge of Good Clinical Practice (GCP) or clinical research operations.


Apply