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Clinical Study Associate Jobs in Indiana (NOW HIRING)

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Clinical Study Associate information

See Indiana salary details

$12

$30

$52

How much do clinical study associate jobs pay per hour?

As of Jul 24, 2026, the average hourly pay for clinical study associate in Indiana is $30.01, according to ZipRecruiter salary data. Most workers in this role earn between $20.14 and $39.57 per hour, depending on experience, location, and employer.

What are Clinical Study Associates?

Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.

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

AspectClinical Study AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficialBachelor's degree in health sciences or related field; certifications like CCRP advantageous
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, clinics, research centers
Job FocusMonitoring clinical trials, ensuring protocol compliance, data accuracyManaging daily trial activities, patient recruitment, data collection
Employer & Industry UsageCommonly employed in pharma and CROsPrimarily in healthcare and academic research settings

Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.

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

To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.

What are some common challenges Clinical Study Associates face when managing multiple clinical trials simultaneously?

Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.
What are the most commonly searched types of Clinical Study jobs in Indiana? The most popular types of Clinical Study jobs in Indiana are:
What cities in Indiana are hiring for Clinical Study Associate jobs? Cities in Indiana with the most Clinical Study Associate job openings:
Infographic showing various Clinical Study Associate job openings in Indiana as of July 2026, with employment types broken down into 1% As Needed, 73% Full Time, 23% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $62,426 per year, or $30 per hour.
Associate Scientist - Immunohematology Reference Lab

Associate Scientist - Immunohematology Reference Lab

Versiti, Inc.

Indianapolis, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago


Versiti rating

5.7

Company rating: 5.7 out of 10

Based on 46 frontline employees who took The Breakroom Quiz

789th of 890 rated healthcare providers


Job description

Overview

Versiti is a fusion of donors, scientific curiosity, and precision medicine that recognize the gifts of blood and life are precious. We are home to the world-renowned Blood Research Institute, we enable life saving gifts from our donors, and provide the science behind the medicine through our diagnostic laboratories. Versiti brings together outstanding minds with unparalleled experience in transfusion medicine, transplantation, stem cells and cellular therapies, oncology and genomics, diagnostic lab services, and medical and scientific expertise. This combination of skill and knowledge results in improved patient outcomes, higher quality services and reduced cost of care for hospitals, blood centers, hospital systems, research and educational institutions, and other health care providers. At Versiti, we are passionate about improving the lives of patients and helping our healthcare partners thrive.

Position Summary

Under direction of the Laboratory Manager serves in an associate scientist capacity to learn and perform immunohematology testing on clinical and research specimens for the resolution of serologic problems and provides the correct blood product for transfusion based on these results. In addition to performing these functions, the associate scientist will gain the required knowledge of immunohematology and laboratory transfusion medicine theory to complete training and educational curriculum to successfully obtain the BB (ASCP) certification.

Total Rewards Package

CompensationThe target salary is based on internal averages. Versiti sets salary ranges aligned to local markets in which the job is performed. Compensation decisions take into account internal salary averages and differentiation based on education, experience, skills, and performance. Specific salary and benefits information is shared at the time of the phone screening based on your location and qualifications.BenefitsVersiti provides a comprehensive benefits package based on your job classification. Full-time regular employes are eligible for Medical, Dental, and Vision Plans, Paid Time Off (PTO) and Holidays, Short- and Long-term disability, life insurance, 7% match dollar for dollar 401(k), voluntary programs, discount programs, others.

Responsibilities
  • Duties and responsibilities will increase as the associate scientist progresses based on successful competency assessments and understanding of theory.
  • Handles and processes specimens, ensuring proper identification.
  • Performs serologic and molecular tests according to SOP on clinical, study, QC and research samples.
  • Performs component preparation as ordered by the provider (if applicable to the lab)
  • Issues appropriate products for transfusion. (if applicable to the lab)
  • Recognizes and resolves procedural discrepancies in testing results.
  • Maintains accurate and complete records.
  • Perform reagent preparation
  • Operates laboratory equipment correctly and perform quality control testing on equipment and reagents. Knows acceptable levels of performance.
  • Maintains controlled inventories of reagents and laboratory materials.
  • Interprets laboratory results.
  • Reports laboratory results.
  • Adheres to all required FDA, AABB (American Association of Blood Banks),CLIA (Clinical Laboratory Improvement Act), OSHA (Occupational Safety and Health Administration), and CAP (College of American Pathology) regulations. Follows cGMP (current Good Manufacturing Practices) standards.
  • Listens, anticipates and responds to the needs of internal and external customers and strives to meet expectations.
  • Communicates clearly, accurately and respectfully with customers, donors, and colleagues, ensuring that necessary information is shared.
  • Notifies management or other appropriate persons of problems or issues as appropriate.
  • Works effectively with inter or intra-department(s) and project teams to meet customer needs and organizational goals.
  • Participates in quality and process improvement.
  • Supports and promotes Versiti mission and values, both at work and in the community.
  • Performs other duties as required or assigned which are reasonably within the scope of the duties in this job classification
  • Understands and performs in accordance with all applicable regulatory and compliance requirements
  • Complies with all standard operating policies and procedures
Qualifications

Education

  • Bachelor's Degree from an accredited college or university with a major in biological science or chemistry OR a Bachelor's degree from an accredited college or university with a combination of 30 semester hours in biology and chemistry within or in addition to the Bachelor's degree required

Experience

  • 1-3 years experience working in a laboratory setting preferred

Knowledge, Skills and Abilities

  • Skill in the operation of laboratory equipment, instrument, computer and materials.
  • Effective time managing and organizational skills to perform multiple laboratory tests simultaneously.
  • Maintain accurate, timely records of patient information and laboratory results.
  • Strong detail orientation and analytical ability to evaluate and ensure accuracy of data related to laboratory results and patient information.
  • Effective verbal and written communication skills, including the ability to convey understanding of factual and theoretical information and make recommendations to customers.
  • Effective problem-solving skills.
  • Ability to work independently and as a team member.

Tools and Technology

  • Personal Computer (desktop, laptop, tablet) required
  • General office equipment (computer, printer, fax, copy machine) required
  • Microsoft Suite (Word, Excel, PowerPoint) required
  • General laboratory equipment including centrifuges, automated cell washers and incubator/waterbaths for performing clinical tests. required
  • Molecular instrumentation such as light cyclers required
  • Pipettes (single channel, multi-channel, electronic, etc.) required
  • pH meter, microscopes required
Employment Type: FULL_TIME

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