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Cra Clinical Research Associate Jobs in Indiana (NOW HIRING)

Beacon Health System

Research Nurse (BMG)

Elkhart, IN · On-site

Reports to the Nurse Manager, Clinical Research. Is responsible for the coordination and delivery ... ORGANIZATIONAL RESPONSIBILITIES Associate complies with the following organizational requirements:

Beacon Health System

Research Nurse (BMG)

Elkhart, IN · On-site

Reports to the Nurse Manager, Clinical Research. Is responsible for the coordination and delivery ... ORGANIZATIONAL RESPONSIBILITIES Associate complies with the following organizational requirements:

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Cra Clinical Research Associate information

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$66

How much do cra clinical research associate jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for cra clinical research associate in Indiana is $39.13, according to ZipRecruiter salary data. Most workers in this role earn between $27.45 and $50.10 per hour, depending on experience, location, and employer.

What is a clinical research associate?

CRA Clinical Research Associates are professionals who monitor clinical trials to ensure they are conducted in accordance with regulatory requirements, study protocols, and Good Clinical Practice guidelines. They act as a bridge between the sponsor of a clinical trial and the sites where the trial is conducted, overseeing data collection, patient safety, and compliance. Their responsibilities include site visits, reviewing documentation, and ensuring accurate reporting of study results. CRAs play a critical role in advancing medical research by maintaining the integrity and quality of clinical studies.

What are the key skills and qualifications needed to thrive as a clinical research associate?

To thrive as a Clinical Research Associate (CRA), you need a solid background in life sciences, experience in clinical trial monitoring, and typically a bachelor's degree in a related field. Familiarity with Good Clinical Practice (GCP) guidelines, electronic data capture (EDC) systems, and regulatory requirements is essential, and certifications like ACRP or SOCRA are often advantageous. Strong attention to detail, organizational skills, effective communication, and adaptability help CRAs excel in coordinating studies and collaborating with diverse stakeholders. These skills ensure clinical trials are conducted ethically, efficiently, and in compliance with regulatory standards, safeguarding both data integrity and patient safety.

What are some common challenges faced by clinical research associates when managing multiple clinical trial sites?

CRAs often juggle oversight of multiple clinical trial sites, which can present challenges such as coordinating visits, ensuring consistent protocol adherence, and managing varying site performance. Effective communication and strong organizational skills are crucial, as CRAs need to address site-specific issues, maintain accurate documentation, and ensure timely data collection. Additionally, adapting to diverse team dynamics and staying updated with regulatory requirements across sites are common aspects of the role. Employers typically provide training and support, but successful CRAs proactively develop strategies to manage these complexities.

What is the difference between Cra Clinical Research Associate vs Clinical Trial Coordinator?

AspectCra Clinical Research AssociateClinical Trial Coordinator
CredentialsTypically requires a bachelor's degree in life sciences, nursing, or related field; certifications like CCRP or RAC are commonUsually holds a bachelor's degree in health sciences, nursing, or related field; certifications like CCRP are also beneficial
Work EnvironmentWorks primarily on-site at clinical trial sites, monitoring study progress and complianceCoordinates trial activities, manages schedules, and ensures protocol adherence, often working at trial sites or offices
Employer & IndustryEmployed by pharmaceutical companies, CROs, or research institutions in the clinical research industryEmployed by hospitals, research centers, or pharmaceutical companies to manage trial logistics

While both roles support clinical trials, Cra Clinical Research Associates focus on monitoring and compliance, whereas Clinical Trial Coordinators handle trial logistics and coordination. Both require relevant certifications and work in similar environments within the clinical research industry.

What are popular job titles related to Cra Clinical Research Associate jobs in Indiana? For Cra Clinical Research Associate jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Cra Clinical Research Associate jobs in Indiana look for? The top searched job categories for Cra Clinical Research Associate jobs in Indiana are:
What cities in Indiana are hiring for Cra Clinical Research Associate jobs? Cities in Indiana with the most Cra Clinical Research Associate job openings:
Cra Clinical Research Associate jobs near you
Infographic showing various Cra Clinical Research Associate job openings in Indiana as of August 2026, with employment types broken down into 2% As Needed, 76% Full Time, 16% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $81,398 per year, or $39.1 per hour.

Post Doc Research Associate

Purdue University

West Lafayette, IN • On-site

Full-time

Re-posted 29 days ago

Purdue University rating

7.5

Company rating: 7.5 out of 10

Based on 136 frontline employees who took The Breakroom Quiz

309th of 616 rated colleges and universities

Job description

Post Doc Research Associate
City: West Lafayette
Job Description:
Job Summary
The Kasinski Laboratory at Purdue University is seeking an exceptionally motivated, innovative, and independent Postdoctoral Research Associate to join a highly collaborative research program focused on RNA therapeutics, targeted drug delivery, extracellular vesicle biology, and translational cancer research. Our laboratory is developing next-generation small RNA therapeutics, including chemically modified microRNAs and siRNAs, with the goal of advancing novel cancer treatments toward clinical translation.
The successful candidate will lead independent research projects investigating the design, delivery, mechanism of action, and therapeutic application of RNA-based medicines in cancer. This position offers substantial opportunities for scientific leadership, career development, and direct involvement in translational research efforts spanning fundamental biology, therapeutic development, and commercialization.
The ideal candidate will possess extensive experience in molecular biology and in vivo cancer models and have a strong interest in RNA therapeutics and nucleic acid biology. The candidate will be expected to independently develop research directions, design and execute experiments, analyze and interpret data, prepare manuscripts for publication in high-impact journals, contribute to fellowship and grant applications, and actively participate in mentoring junior laboratory members.
Career Development OpportunitiesThe successful candidate will have opportunities to:
  • Lead high-impact translational research projects.
  • Publish in top-tier scientific journals.
  • Participate in the preparation of NIH, DoD, foundation, and industry-sponsored grant applications.
  • Develop skills in therapeutic development, intellectual property, and commercialization through interactions with LigamiR Therapeutics and other translational partners.
  • Receive mentorship tailored toward career advancement in academia, biotechnology, pharmaceutical research, or entrepreneurial ventures.

Education
  • Ph.D. in Molecular Biology, Cancer Biology, Genetics, Pharmacology, Biomedical Sciences, or a closely related field.

Experience
Required Qualifications
  • Ph.D. in Molecular Biology, Cancer Biology, Genetics, Pharmacology, Biomedical Sciences, or a closely related field.
  • Strong expertise in molecular and cellular biology techniques, including nucleic acid manipulation, cloning, gene expression analysis, CRISPR-based approaches, protein analysis, and functional cellular assays.
  • Extensive hands-on experience with in vivo mouse studies, including tumor implantation models, therapeutic efficacy studies, tissue collection, and downstream molecular analyses.
  • Demonstrated record of scientific productivity, including first-author publications in peer-reviewed journals.
  • Excellent written and oral communication skills.
  • Ability to work both independently and collaboratively in a fast-paced, multidisciplinary research environment.

Preferred Qualifications
  • Experience with RNA therapeutics, including microRNAs, siRNAs, antisense oligonucleotides, mRNA technologies, or related nucleic acid-based platforms.
  • Familiarity with chemically modified RNAs, oligonucleotide design, RNA chemistry, or RNA structure-function relationships.
  • Experience evaluating therapeutic efficacy, pharmacodynamics, pharmacokinetics, biodistribution, or target engagement in preclinical models.
  • Experience with cancer biology, tumor microenvironment studies, extracellular vesicle biology, or translational oncology research.
  • Experience with next-generation sequencing technologies and computational analysis of genomic or transcriptomic datasets.
  • Previous involvement in preparing fellowship applications, grant proposals, or patent disclosures.

Desired Skills and Personal Attributes
  • Highly driven scientist with a strong desire to make impactful discoveries and advance technologies toward clinical application.
  • Demonstrated ability to think creatively, identify important scientific questions, and develop innovative experimental approaches.
  • Strong commitment to scientific rigor, reproducibility, and excellence.
  • Ability to independently drive multiple projects from conception through publication.
  • Interest in pursuing external fellowship funding and contributing to grant development.
  • Excellent organizational, project management, and problem-solving skills.
  • Collaborative team player who contributes positively to laboratory culture and enjoys working with scientists from diverse backgrounds and disciplines.
  • Strong interpersonal skills, professionalism, and a willingness to mentor graduate and undergraduate trainees.
  • Enthusiasm for working at the interface of basic science, translational research, and therapeutic development.

FLSA Status
Exempt

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