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Clinical Trials Associate Jobs in Indiana (NOW HIRING)

Indiana University

Clinical Research Technician

Indianapolis, IN · On-site

$37K - $42K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

Assists in the conduct of clinical research studies or trials following established protocols and ... Associate's degree in an allied health profession plus 1 year of patient-related or research ...

Indiana University

Clinical Research Coordinator

Indianapolis, IN · On-site

$23.25 - $30.75/hr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

The division has multiple research laboratories, programs, and clinical trials conducting studies ... OR * Associate's degree in science or a health-related field and 3 years of clinical research ...

Indiana University

Clinical Research Coordinator

Indianapolis, IN · On-site

$23.25 - $30.75/hr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

The division has multiple research laboratories, programs, and clinical trials conducting studies ... OR * Associate's degree in science or a health-related field and 3 years of clinical research ...

Indiana University

Clinical Research Coordinator

Indianapolis, IN · On-site

$50K - $60K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

... trials in rare and common genetic diseases. Job Summary * Initiates and conducts protocol review ... OR * Associate's degree in science or a health-related field and 2 years of clinical research ...

Indiana University

Clinical Research Coordinator

Indianapolis, IN · On-site

$50K - $60K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

... trials in rare and common genetic diseases. Job Summary * Initiates and conducts protocol review ... OR * Associate's degree in science or a health-related field and 2 years of clinical research ...

Genezen

Senior/Lead Associate, QA Operations

Indianapolis, IN · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... clinical trials and are proud to be a part of the process that leads to new cures. WORKING AT ... Review work performed by junior associates for accuracy, completeness, and compliance prior to ...

New

Indiana University

Clinical Research Coordinator

Indianapolis, IN · On-site

$23.25 - $30.75/hr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

... and clinical trials in rare and common genetic diseases. Job Summary * Oversees day-to-day ... Society of Clinical Research Associates (SOCRA)/ Association of Clinical Research Professionals ...

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Showing results 21-40

All JobsClinical Trials Associate JobsClinical Trials Associate Jobs in Indiana

Clinical Trials Associate information

See Indiana salary details

$16

$38

$66

How much do clinical trials associate jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for clinical trials associate in Indiana is $38.05, according to ZipRecruiter salary data. Most workers in this role earn between $30.67 and $41.88 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical trials associate, and why are they important?

To thrive as a Clinical Trials Associate, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, typically supported by a life sciences degree. Familiarity with systems such as electronic data capture (EDC), clinical trial management systems (CTMS), and knowledge of Good Clinical Practice (GCP) guidelines or related certifications is important. Strong organizational skills, attention to detail, and effective communication help you excel in coordinating study activities and collaborating with diverse teams. These skills ensure accurate trial execution, regulatory adherence, and successful study outcomes.

What do I need to be a clinical trials associate?

To become a clinical trials associate, candidates typically need a bachelor's degree in life sciences, healthcare, or a related field. Relevant skills include knowledge of Good Clinical Practice (GCP), attention to detail, and experience with clinical trial management systems; certifications like CCRP can be advantageous.

What are some common challenges faced by clinical trials associates, and how can they be managed effectively?

Clinical Trials Associates often face challenges such as coordinating with multiple stakeholders, managing tight deadlines, and ensuring strict compliance with regulatory guidelines. Balancing administrative tasks with participant communication requires strong organizational skills and attention to detail. Staying proactive in communication, utilizing project management tools, and seeking guidance from senior team members can help manage these challenges effectively while fostering a collaborative team environment.

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

AspectClinical Trials AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like ACRP or SOCRA are commonBachelor's degree in health sciences or related field; certifications like CCRP are advantageous
Work EnvironmentTypically works in clinical trial sites, pharmaceutical companies, or CROsWorks directly at clinical sites, hospitals, or research centers
Job FocusSupports trial setup, data entry, and regulatory complianceManages patient recruitment, scheduling, and data collection

While both roles support clinical research, Clinical Trials Associates primarily focus on trial logistics and compliance, whereas Clinical Research Coordinators handle patient interactions and site management. Both positions require similar educational backgrounds and certifications, often working in the same environments, but their daily responsibilities differ.

What is a clinical trials associate?

Clinical Trials Associates (CTAs) are professionals who support the planning, coordination, and administration of clinical research studies, often working under the supervision of Clinical Research Coordinators or Managers. Their responsibilities typically include maintaining study documentation, ensuring regulatory compliance, assisting with data collection, and communicating with study sites. CTAs play a critical role in ensuring that clinical trials run smoothly and adhere to strict protocols and guidelines. Their work helps bring new medical treatments and therapies to market safely and efficiently.

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 Associate jobs?

Cities in Indiana with the most Clinical Trials Associate job openings:

Clinical Trials Associate jobs near you
Infographic showing various Clinical Trials Associate job openings in Indiana as of August 2026, with employment types broken down into 3% As Needed, 73% Full Time, 17% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $79,141 per year, or $38 per hour.

Clinical Research Coordinator II

Iterative Health

New Albany, IN • On-site

$22.50 - $29.75/hr

Full-time

Re-posted 15 days ago

Job description

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.
We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.
As a Clinical Research Coordinator II (CRC II) at Iterative Health you will play a critical role in the successful execution of clinical trials by independently coordinating daily study activities and ensuring compliance with protocol requirements, regulatory standards, and patient safety guidelines.
This role is responsible for managing complex studies with minimal oversight while partnering closely with patients, investigators, sponsors, CROs, and internal teams to drive high-quality study execution and enrollment success.
Where You'll Drive Impact
  • Independently coordinate and manage industry-sponsored clinical trials from study start-up through closeout with minimal supervision
  • Manage complex study visit schedules and protocol-related activities while ensuring adherence to study timelines and requirements
  • Lead patient recruitment and retention efforts including chart review, patient outreach, informed consent discussions, and enrollment tracking to support study enrollment goals
  • Conduct protocol-required patient visits and assessments in accordance with study protocols, GCP guidelines, and site SOPs
  • Perform protocol-required clinical procedures including vital signs, ECGs, specimen collection, investigational product accountability, and phlebotomy, as permitted by applicable regulations, training, and organizational policy
  • Process laboratory specimens and prepare shipments in accordance with protocol requirements and applicable IATA regulations
  • Maintain accurate, complete, and timely study documentation including source records, informed consent forms, CTMS updates, and case report forms
  • Ensure high-quality data entry and timely resolution of data queries in accordance with sponsor expectations and established timelines
  • Serve as a primary point of contact for study participants throughout study participation
  • Maintain ongoing communication with sponsors, CROs, investigators, site leadership, and internal teams to proactively resolve study-related issues
  • Prepare for and support sponsor, CRO, and regulatory monitoring visits, audits, and inspections
  • Review safety reports and ensure appropriate investigator review and documentation in a timely manner
  • Maintain inventory and organization of study equipment, supplies, and investigational products onsite
  • Contribute to process improvement initiatives to enhance site performance, operational efficiency, and patient experience
  • Support the protection of human research participants in compliance with federal regulations, GCP, HIPAA, and institutional policies
  • Maintain compliance with all site SOPs, privacy standards, and research protocols
  • May support onboarding and mentorship of junior research staff and coordinators
  • Perform job related duties as requested

What You Bring to the Team
  • Associate's or Bachelor's degree in a scientific, healthcare, or related discipline required
  • 3-5 years of clinical research or healthcare experience required
  • CCRC® - Certified Clinical Research Coordinator or CCRP® - Certified Clinical Research Professional or equivalent clinical research certification preferred
  • Strong organizational skills and attention to detail
  • Ability to manage competing priorities in a fast-paced environment
  • Ability to read, interpret, and apply research protocols and clinic policies
  • Proficiency with CTMS, EDC systems, and standard office software applications
  • Familiarity with CTMS or EDC systems preferred
Physical Requirements
  • Ability to sit, stand, and move throughout clinical and office environments for extended periods of time
  • Ability to lift and move up to 25 pounds as needed

At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.

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