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Clinical Trials Manager Jobs in Indiana (NOW HIRING)

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Clinical Trials Manager information

See Indiana salary details

$27

$59

$91

How much do clinical trials manager jobs pay per hour?

As of Aug 2, 2026, the average hourly pay for clinical trials manager in Indiana is $59.49, according to ZipRecruiter salary data. Most workers in this role earn between $48.27 and $67.02 per hour, depending on experience, location, and employer.

What does a Clinical Trials Manager do?

A Clinical Trials Manager oversees the planning, coordination, and execution of clinical trials to ensure they are conducted safely, efficiently, and in compliance with regulatory requirements. They manage teams, budgets, timelines, and communication between stakeholders such as sponsors, investigators, and regulatory bodies. Their responsibilities also include monitoring trial progress, resolving issues, and ensuring data integrity throughout the study.

What are the key skills and qualifications needed to thrive as a Clinical Trials Manager, and why are they important?

To thrive as a Clinical Trials Manager, you need expertise in clinical research processes, regulatory compliance, and project management, often supported by a degree in life sciences and experience in clinical trial coordination. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and relevant certifications such as ACRP or SOCRA are typically required. Strong leadership, attention to detail, and effective communication are vital soft skills for managing teams and ensuring protocol adherence. These skills and qualities are crucial for maintaining trial integrity, regulatory compliance, and successful project outcomes.

What is the difference between Clinical Trials Manager vs Clinical Research Coordinator?

AspectClinical Trials ManagerClinical Research Coordinator
ResponsibilitiesOversees entire clinical trial process, manages teams, ensures compliance, and handles budgets.Assists with patient recruitment, data collection, and site coordination under supervision.
Required CredentialsBachelor’s or higher in life sciences, often with project management experience.Typically holds a bachelor’s degree in health sciences or related field; certification may be preferred.
Work EnvironmentWorks in clinical trial sites, research organizations, or pharmaceutical companies.Primarily works at clinical sites, hospitals, or research facilities.

In summary, Clinical Trials Managers oversee the entire trial process and manage teams, while Clinical Research Coordinators support daily trial activities at the site level. Both roles require relevant education and work in clinical research settings, but differ in scope and responsibilities.

What are some common challenges faced by Clinical Trials Managers and how can they be addressed?

Clinical Trials Managers often encounter challenges such as ensuring regulatory compliance, managing complex timelines, and coordinating communication among diverse stakeholders. Balancing the needs of sponsors, investigators, and regulatory bodies requires strong organizational skills and attention to detail. Proactively addressing these challenges involves implementing robust project management tools, maintaining clear documentation, and fostering open communication within the team. Building relationships with site staff and regularly updating all parties can help anticipate issues early and keep trials on track.
What are the most commonly searched types of Clinical Trials jobs in Indiana? The most popular types of Clinical Trials jobs in Indiana are:
What cities in Indiana are hiring for Clinical Trials Manager jobs? Cities in Indiana with the most Clinical Trials Manager job openings:
Infographic showing various Clinical Trials Manager job openings in Indiana as of July 2026, with employment types broken down into 2% As Needed, 76% Full Time, 14% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $123,736 per year, or $59.5 per hour.

Clinical Trials Manager - Patient Engagement (Direct Portfolio Project Manager) (Hybrid - Indianapol

Pharmavise

Indianapolis, IN • On-site

Contractor

Re-posted 25 days ago


Job description


Our Fortune 500 Pharmaceutical client has an exciting opportunity for a Clinical Trials Manager.
Job Summary:
We are seeking a Clinical Trials Manager - Patient Engagement to develop and deliver patient recruitment and retention strategies across clinical trial programs. This role combines strategic thinking, hands-on project management, and deep clinical trial experience to support patient-centered, compliant, and efficient trial execution.
This is a strong fit for someone who has worked closely in clinical trials, has coordinated or managed trial projects, and has directly supported patient engagement, recruitment, and/or retention efforts.
What You'll Do
  • Develop and implement patient recruitment and retention strategies for clinical trials and programs

  • Lead and manage trial-related projects and initiatives, ensuring efficient delivery, compliance, and adherence to regulatory and ERB requirements

  • Make informed, day-to-day decisions by understanding repeatable processes, recognizing nuances, and determining next steps based on fact-dependent parameters

  • Partner closely with cross-functional teams and stakeholders to align on strategy, execution, and priorities

  • Support clinical trial documentation and ensure record-keeping and retention compliance

  • Operate comfortably in a deadline-driven environment, prioritizing work based on defined processes and associated timelines

  • Take direction and feedback well, applying learning quickly and retaining instructions to continuously improve delivery

  • Apply lessons learned and best practices to improve patient engagement approaches and standardize processes

What We're Looking For
  • 5+ years of clinical trial experience

  • 3+ years of coordination and/or project management experience supporting clinical or cross-functional initiatives

  • 3+ years of patient engagement experience, including patient recruitment and retention strategies for clinical trials

  • Bachelor's degree in a scientific or health-related field

  • Strong understanding of clinical trial operations, compliance, and regulatory requirements

  • Comfortable working across multiple systems and technologies

  • Strong communication, organization, and collaboration skills

  • Passion for improving patient access, diversity, and inclusion in clinical research

Key Requirements for this role:
  • Onsite / Hybrid (Indianapolis, IN)

  • 5+ years of clinical trial experience

  • 3+ years of patient engagement experience

  • Project management and/or clinical coordinator experience

Other Details:
  • Schedule: Full Time

  • Work Setup: Hybrid in Indianapolis, IN

  • Contract Length: 18 months with possible contract extension