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Clinical Trials Jobs in Indiana (NOW HIRING)

Actalent

Clinical Research Coordinator

Indianapolis, IN · On-site

$21.25 - $28.25/hr

Recruit patients for industry-sponsored drug trials by clearly explaining study opportunities and ... Clinical research experience, with a strong preference for at least 2 years as a Clinical Research ...

Actalent

Clinical Research Nurse

Indianapolis, IN · On-site

$28 - $37/hr

Support the conduct of oncology clinical trials across Phases I-IV, ensuring adherence to study protocols and timelines. * Assist with patient visits by scheduling, preparing visit documentation, and ...

Actalent

Clinical Research Nurse

Indianapolis, IN · On-site

$28 - $37/hr

Support the conduct of oncology clinical trials across Phases I-IV, ensuring adherence to study protocols and timelines. * Assist with patient visits by scheduling, preparing visit documentation, and ...

Actalent

Oncology RN - Clinical Research

Indianapolis, IN · On-site

$40 - $45/hr

Clinical Research Nurse - Oncology (Phase I Trials) This clinical research nurse role focuses on supporting phase I oncology clinical trials by providing direct patient care during study visits. The ...

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Clinical Trials information

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How much do clinical trials jobs pay per hour?

As of Jul 30, 2026, the average hourly pay for clinical trials 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 are the key skills and qualifications needed to thrive in the Clinical Trials position, and why are they important?

To thrive in Clinical Trials roles, you need a strong understanding of clinical research principles, Good Clinical Practice (GCP) guidelines, and a background in life sciences or healthcare. Familiarity with electronic data capture (EDC) systems, regulatory compliance software, and relevant certifications such as GCP or CCRA is highly valuable. Attention to detail, organizational skills, and effective communication enable collaboration across multidisciplinary teams. These competencies are crucial for ensuring protocol adherence, data integrity, and the successful execution of trial activities.

How to get into clinical trial work?

To work in clinical trials, individuals typically need a background in healthcare, life sciences, or related fields, along with relevant certifications such as Good Clinical Practice (GCP). Entry-level roles often require strong organizational skills, attention to detail, and familiarity with regulatory requirements; some positions may also require a bachelor's degree or higher. Gaining experience through internships or training programs can improve job prospects in this field.

How much money can I make doing clinical trials?

Clinical trial participants can earn anywhere from $50 to several thousand dollars depending on the study's duration, complexity, and requirements. Compensation varies based on factors such as the type of trial, location, and whether medical procedures or tests are involved. Participants often receive payment after completing the study or specific milestones within it.

Which clinical trials pay the most?

Clinical trials involving high-risk or complex treatments, such as oncology or rare disease studies, often offer higher compensation to participants and staff. Additionally, roles like clinical research coordinators or principal investigators in well-funded trials tend to earn more due to their responsibilities and expertise. Compensation varies based on trial phase, location, and the level of experience required.

What are some common career paths or advancement opportunities for professionals working in Clinical Trials?

Many professionals in Clinical Trials start their careers as Clinical Research Coordinators, Clinical Research Associates, or Data Managers. With experience, you can advance to roles such as Senior Clinical Research Associate, Clinical Trial Manager, or Project Manager, and potentially move into areas like regulatory affairs, medical writing, or quality assurance. The role offers continuous learning opportunities, exposure to innovative therapies, and often provides the chance to lead larger, more complex studies as you progress. Advancement is typically supported by additional certifications, strong performance, and a proactive approach to professional development. Teamwork and networking within the industry can also open new doors for growth.

Are clinical trial jobs in high demand?

Clinical trial jobs are in high demand due to the ongoing need for new medical treatments and the growth of the healthcare industry. Positions such as clinical research coordinators and data managers are often sought after, especially for those with relevant certifications and experience in regulatory compliance and data management tools.

What is a Clinical Trials job?

A Clinical Trials job involves managing, coordinating, or supporting research studies that evaluate the safety and effectiveness of medical treatments, drugs, or devices. Professionals in this field work on trial design, patient recruitment, data collection, regulatory compliance, and reporting results. Roles can range from clinical research coordinators to trial managers and regulatory specialists. The goal is to ensure that studies follow ethical guidelines and produce reliable data for medical advancements.

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 are popular job titles related to Clinical Trials jobs in Indiana? For Clinical Trials jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Clinical Trials jobs in Indiana look for? The top searched job categories for Clinical Trials jobs in Indiana are:
What cities in Indiana are hiring for Clinical Trials jobs? Cities in Indiana with the most Clinical Trials job openings:
Clinical Trials jobs near you
Infographic showing various Clinical Trials job openings in Indiana as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 18% Part Time, and 7% 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 23 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

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