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Clinical Research Operations Manager Jobs in Indiana

MediSphere Medical Research Center, LLC

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Clinical Research Assistant II

Evansville, IN · On-site

Documentation & Data Management * Accurately complete source documentation during participant ... Maintain study supply inventory. * Assist with general office and clinical operations. Other ...

DaVita

$23.50 - $31/hr

Experience in managing confidential information and/or issues using discretion and Judgment * Certified Clinical Research Coordinator (SOCRA or ACRP) - preferred DaVita Clinical Research (DCR), a ...

DS Research

Medical Assistant, Clinical Research

Clarksville, IN · On-site

$16.25 - $20.75/hr

In this role, you will support our clinical research efforts and contribute to the advancement of ... time management skills - Proficient computer skills, including MS Office Suite and Google Docs ...

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Clinical Research Operations Manager information

See Indiana salary details

$33.3K

$93.3K

$177.5K

How much do clinical research operations manager jobs pay per year?

As of Aug 31, 2026, the average yearly pay for clinical research operations manager in Indiana is $93,290.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,000.00 and $108,000.00 per year, depending on experience, location, and employer.

What does a clinical research operations manager do?

A Clinical Research Operations Manager oversees the daily operations of clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory standards. They coordinate between research staff, sponsors, and regulatory bodies, manage budgets and timelines, and ensure proper documentation and reporting. Their role is essential in maintaining the quality and integrity of clinical studies from start to finish.

How does a clinical research operations manager collaborate with cross-functional teams during a study?

As a Clinical Research Operations Manager, you will work closely with cross-functional teams including clinical trial coordinators, data managers, regulatory affairs specialists, and principal investigators. Your role involves facilitating clear communication between departments, ensuring that study milestones are met, and resolving operational issues as they arise. Regular meetings and status updates are common, and you'll often act as a liaison to keep all stakeholders aligned on study objectives, timelines, and compliance requirements. This collaborative approach is crucial for maintaining study integrity and ensuring successful trial outcomes.

What are the key skills and qualifications needed to thrive as a clinical research operations manager, and why are they important?

To thrive as a Clinical Research Operations Manager, you need a solid background in clinical research, regulatory compliance, and project management, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and certifications such as ACRP or SOCRA are highly valuable. Leadership, problem-solving, and excellent organizational and communication skills help you manage teams and collaborate effectively with stakeholders. These skills and qualities are crucial for ensuring the successful execution of clinical trials while maintaining regulatory standards and operational efficiency.

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

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

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

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

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

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

Clinical Research Operations Manager jobs near you
Infographic showing various Clinical Research Operations Manager job openings in Indiana as of August 2026, with employment types broken down into 84% Full Time, 13% Part Time, 1% Temporary, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $93,290 per year, or $44.9 per hour.

Mobile Clinical Research Operations Associate

Medasource

Greenwood, IN • On-site

Other

Posted 10 days ago

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