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Clinical Research Associate Remote Jobs in Indiana

IQVIA

Associate Principal Scientist

Indianapolis, IN · On-site +1

$80K - $167K/yr

We are seeking an Associate Principal Scientist to join IQVIA Laboratories in Indiana. We hire ... IQVIA is a leading global provider of clinical research services, commercial insights and health ...

Intuitive

Clinical Territory Associate

South Bend, IN · On-site +1

Primary Function of Position The Clinical Territory Associate (CTA) is a 24+ month developmental role that will partner with the Indiana team to gain knowledge in all aspects of our business to ...

Intuitive

Clinical Territory Associate

Fort Wayne, IN · On-site +1

Primary Function of Position The Clinical Territory Associate (CTA) is a 24+ month developmental sales role that will partner with the Indiana team to gain knowledge in all aspects of our business to ...

Briljent

Clinical Auditor - RN

Indianapolis, IN · Remote

This is a remote position with occasional travel required within Indiana. Key Responsibilities ... Research Indiana Medicaid rules and maintain internal repositories of bulletins, policies, and ...

ProPharma Group

With deep domain expertise in regulatory sciences, clinical research solutions, quality ... Remote working - with over 85% of our workforce successfully working from home, we can offer a ...

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Clinical Research Associate Remote information

See Indiana salary details

$34.3K

$89.7K

$136.6K

How much do clinical research associate remote jobs pay per year?

As of Jul 19, 2026, the average yearly pay for clinical research associate remote in Indiana is $89,746.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,500.00 and $121,800.00 per year, depending on experience, location, and employer.

What does a Clinical Research Associate do when working remotely?

A Clinical Research Associate (CRA) working remotely is responsible for monitoring clinical trials to ensure they comply with regulatory requirements and study protocols. They coordinate with clinical sites, review data, ensure proper documentation, and communicate findings with research teams—all from a remote location. While they may occasionally travel for on-site visits, most of their tasks, such as reviewing electronic records, participating in virtual meetings, and managing trial documentation, are performed online. Remote CRAs play a vital role in maintaining the integrity and quality of clinical studies.

What are some common challenges faced by Clinical Research Associates working remotely, and how can they be addressed?

Remote Clinical Research Associates often face challenges such as coordinating across different time zones, maintaining clear communication with site staff, and ensuring data integrity without being physically present. These challenges can be addressed by leveraging robust digital tools for project management and communication, setting clear expectations with research sites, and establishing regular virtual check-ins. Staying organized, proactive, and responsive is key to successfully managing multiple studies and fostering effective collaboration from a remote environment.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate (Remote), and why are they important?

To excel as a Clinical Research Associate (Remote), you generally need a background in life sciences or a related field, experience with clinical trial processes, and knowledge of regulatory guidelines like GCP. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and relevant certifications such as ACRP or SOCRA are highly valuable. Strong organizational, communication, and problem-solving skills are essential for managing remote monitoring and collaborating with research teams. These competencies ensure data integrity, regulatory compliance, and effective coordination across geographically dispersed clinical trial sites.
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Clinical Research Associate Remote jobs near you
Associate Principal Scientist

Associate Principal Scientist

IQVIA

Indianapolis, IN • On-site, Remote

$80K - $167K/yr

Full-time

Medical, Life

Re-posted 20 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

55th of 210 rated it services

Job description

We are seeking an Associate Principal Scientist to join IQVIA Laboratories in Indiana.
We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.
Job Summary:
The Associate Principal Scientist provides scientific leadership in in vitro and in vivo metabolism and biotransformation studies, with a primary focus on mass spectrometry data interpretation, metabolite profiling, and rapid, highquality reporting to support drug discovery and development programs.
What You'll Be Doing:
  • Independently analyze, interpret, and report MS and MS/MS data from in vitro and in vivo metabolism studies
  • Develop, implement, and troubleshoot analytical methods for metabolite identification and profiling
  • Assign metabolite structures and propose metabolic pathways using sound scientific judgment
  • Manage study flow to ensure highquality, ontime delivery of reports in a fastpaced, highthroughput environment
  • Serve as a scientific resource for complex data interpretation, assay development, and problem solving
  • Collaborate with project teams and interact with clients to discuss scientific principles and study outcomes
  • Mentor and provide guidance to junior scientists and new team members
What We Are Looking For:
  • PhD, Master's, or Bachelor's degree in chemistry, biochemistry, biology, or a related scientific discipline.
  • Indepth experience with drug metabolism and biotransformation, including metabolite profiling and structural elucidation
  • Strong expertise in mass spectrometry, including MS and MS/MS data collection and interpretation
  • Handson knowledge of analytical method development and troubleshooting for metabolism studies
  • Other Equivalent combination of education, training, and experience may be accepted in lieu of degree
The Knowledge, Skills and Abilities Needed for This Role:
  • Ability to rapidly interpret complex data and produce clear, concise scientific reports under tight timelines
  • Strong understanding of ADME metabolism principles and highthroughput discovery workflows
  • Excellent written and verbal communication skills with the ability to engage internal teams and clients
  • Demonstrated attention to detail, sound scientific judgment, and commitment to data quality
  • Ability to manage multiple projects simultaneously in a productiondriven CRO environment
What We Offer You:
We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social wellbeing so they can thrive at home and at work, at any stage of their wellbeing journey.
To learn more about our benefits, visit https://jobs.iqvia.com/benefits.
If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $80,200.00 - $167,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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