1

Research Associate Jobs in Angola, IN (NOW HIRING)

Fashion Team Associate

Auburn, IN · On-site

$14 - $27/hr

Mid-Shift, Closing Location Walmart Supercenter #1570 505 TOURING DR, AUBURN, IN, 46706, US Job Overview Fashion Team Associate Benefits & perks At Walmart, we offer competitive pay as well as ...

Mid-Shift, Closing Location Walmart Supercenter #1388 2501 E NORTH ST, KENDALLVILLE, IN, 46755, US Job Overview Fashion Team Associate Benefits & perks At Walmart, we offer competitive pay as well as ...

Mid-Shift, Closing Location Walmart Supercenter #1388 2501 E NORTH ST, KENDALLVILLE, IN, 46755, US Job Overview Home associates greet customers on the salesfloor, offer them assistance and recommend ...

Mid-Shift, Closing Location Walmart Supercenter #1593 800 E CHICAGO ST, COLDWATER, MI, 49036, US Job Overview Front End Checkout associates run our registers. They smile, greet and thank customers ...

Mid-Shift, Closing Location Walmart Supercenter #1709 2016 N WAYNE ST, ANGOLA, IN, 46703, US Job Overview Entertainment associates greet customers on the salesfloor and offer them assistance. They ...

Mid-Shift, Closing Location Walmart Supercenter #1570 505 TOURING DR, AUBURN, IN, 46706, US Job Overview Entertainment associates greet customers on the salesfloor and offer them assistance. They are ...

Mid-Shift, Closing Location Walmart Supercenter #1388 2501 E NORTH ST, KENDALLVILLE, IN, 46755, US Job Overview Entertainment associates greet customers on the salesfloor and offer them assistance.

Mid-Shift, Closing Location Walmart Supercenter #2191 1215 S MAIN ST, BRYAN, OH, 43506, US Job Overview Front End Service associates are focused on compliance and customer service. They smile, greet ...

Opening, Morning, Mid-Shift, Closing Location Walmart Supercenter #2191 1215 S MAIN ST, BRYAN, OH, 43506, US Job Overview Online Order Filling associates have one focus: to fill and dispense online ...

Opening, Morning, Mid-Shift, Closing Location Walmart Supercenter #1570 505 TOURING DR, AUBURN, IN, 46706, US Job Overview Online Order Filling associates have one focus: to fill and dispense online ...

Opening, Morning, Mid-Shift, Closing Location Walmart Supercenter #1709 2016 N WAYNE ST, ANGOLA, IN, 46703, US Job Overview Online Order Filling associates have one focus: to fill and dispense online ...

Opening, Morning Location Walmart Supercenter #1771 1500 S CENTERVILLE RD, STURGIS, MI, 49091, US Job Overview Online Order Filling associates have one focus: to fill and dispense online orders. They ...

Opening, Morning, Mid-Shift, Closing Location Walmart Supercenter #2191 1215 S MAIN ST, BRYAN, OH, 43506, US Job Overview Online Order Filling associates have one focus: to fill and dispense online ...

Licensed Optical Manager

Angola, IN · On-site

$27 - $37/hr

... with Associates and listening to concerns researching issues reviewing Company policies and procedures and suggesting resolution for Associates Coordinates completes and oversees jobrelated ...

next page

Showing results 1-20

Research Associate information

See Angola, IN salary details

$15

$30

$44

How much do research associate jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for research associate in Angola, IN is $30.59, according to ZipRecruiter salary data. Most workers in this role earn between $24.62 and $34.81 per hour, depending on experience, location, and employer.

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

To thrive as a Research Associate, you need a strong background in research methodology, data analysis, and subject-specific knowledge, typically supported by a relevant bachelor's or master's degree. Familiarity with statistical software (such as SPSS, R, or Python), laboratory equipment, and research databases is often essential. Attention to detail, critical thinking, and clear written and verbal communication skills set outstanding Research Associates apart. These skills ensure accurate data collection, effective collaboration, and the production of reliable, impactful research outcomes.

What is a research associate?

Research Associates are professionals who support research projects in academic, scientific, or business settings. They assist with designing studies, collecting and analyzing data, and preparing reports or publications. Research Associates often work under the supervision of principal investigators or senior researchers, contributing their expertise to advance the goals of the project. Their responsibilities can vary depending on the field, but typically involve both administrative and hands-on research tasks.

How much does a research associate earn?

Research associates typically earn a median annual salary ranging from $40,000 to $60,000, depending on experience, education, and industry. Salaries can vary based on location, specialization, and the organization’s size, with some roles offering additional benefits such as research funding or professional development opportunities.

What does a research associate do?

As a research associate, you conduct research and analysis as directed by a senior researcher or project manager. Researchers work in a number of fields, including medical science, the social sciences, natural sciences, finance, management, and academia. Your specific duties and responsibilities differ depending on the field in which you work, but some features of your work are similar across industries. You typically do primary and secondary source research, organize and process data, analyze said data, and report on your findings to lead researchers or clinicians.

What are some typical challenges a research associate might face when managing multiple research projects simultaneously?

As a Research Associate, juggling multiple projects often requires strong organizational skills and the ability to prioritize tasks effectively. You might encounter challenges such as balancing deadlines, coordinating with various team members, and adapting to shifting project goals or data requirements. Effective communication and proactive time management are essential to ensure each project progresses smoothly and meets its milestones. Many teams use project management tools and regular check-ins to help mitigate these challenges and support collaboration.

What is the difference between Research Associate vs Research Scientist?

AspectResearch AssociateResearch Scientist
Required CredentialsBachelor's or Master's degree in relevant fieldMaster's or PhD in relevant field
Work EnvironmentLaboratories, research institutions, universitiesLaboratories, research institutions, industry settings
Employer & Industry UsageAcademic, government, non-profitAcademic, industry, biotech, pharma
Common Search & ComparisonYesYes

The main difference between a Research Associate and a Research Scientist lies in their educational requirements and level of experience. Research Associates typically hold a bachelor's or master's degree and assist in research projects, while Research Scientists usually have a PhD and lead research efforts. Both roles work in similar environments like labs and research institutions, but Research Scientists often have more independence and responsibility.

Is a research associate a good career?

A research associate role is a valuable entry-level position in academia, industry, or government, involving data collection, analysis, and reporting. It offers opportunities to develop research skills, collaborate with professionals, and advance to higher-level positions with experience and additional qualifications.
What are the most commonly searched types of Research jobs in Angola, IN? The most popular types of Research jobs in Angola, IN are:
What cities near Angola, IN are hiring for Research Associate jobs? Cities near Angola, IN with the most Research Associate job openings:
Infographic showing various Research Associate job openings in Angola, IN as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $63,633 per year, or $30.6 per hour.

Clinical Research Coordinator

American Oncology Network

Wayne, IN • On-site

$23.85 - $41.96/hr

Full-time

Posted 14 days ago


American Oncology Network rating

6.7

Company rating: 6.7 out of 10

Based on 30 frontline employees who took The Breakroom Quiz

532nd of 887 rated healthcare providers


Job description

Location:
Fort Wayne Medical Oncology and Hematology
Pay Range:
$23.85 - $41.96
Job Description Summary:
Responsible for the performance of the research study under the medical supervision of the Principal Investigator. Clinical Research Coordinator II (non-RN) performs tasks independently, consistently and accurately, and demonstrate that they have achieved a moderate level of expertise in all of their skills and abilities resulting in high quality work
Primary responsibility includes complex types of study designs (phase 1-3, multi-cohort, interventional trial design) and associated study procedures. Administratively and clinically manage an average 10 clinical trials open to accrual annually and/or active (on study treatment) patient volume over 25 annually
Demonstrates working knowledge of all facets of role, relevant regulations, and organizational and departmental policies and procedures. Performs other duties and projects as assigned. Performs all duties in accordance with regulatory requirements and organizational policies and procedures.
Primary Key Performance Areas:
KPA 1 - Protocol Comprehension and Implementation: Coordination of care for patients on clinical research protocols in accordance with GCP, ICH/FDA guidelines and requirements.
  • Demonstrate an understanding of protocol elements / requirements and demonstrate the ability to execute study procedures. Demonstrate the ability to anticipate and mitigate the potential for protocol non-compliance.
  • Conduct protocol feasibility assessments and complete feasibility/site assessment questionnaires
  • Assess subjects on the basis of inclusion/exclusion criteria and demonstrate the ability to evaluate and document subject eligibility independently.
  • Reviews draft informed consent documents in compliance with regulatory requirements and GCPs. Conduct an informed consent discussion in compliance with SOPs
  • Review and interpret diagnostic test results and related documentation required per protocol
  • Follows process for capturing, assessing, determining causal relationship of adverse events to the investigational product, investigator oversight, reporting and following up on adverse events. Recognize, report and follow up on all types of adverse events
  • Maintain accurate records of the receipt, inventory, distribution and destruction of study-related materials / investigational products and research specimens.
  • Ensure that the investigational drug is received, stored, and documented, and that excess materials are returned to the sponsor according to sponsor guidelines and in accordance with Code of Federal Regulations. Assesses and manages investigational products that have been compromised.

KPA 2 - Regulatory and Data Integrity
  • Understanding of the IRB/IEC review, key elements of review considerations, approval and reporting requirements for the site. Complete all IRB/IEC-related documents over the course of a clinical study. Maintains site credentials and ensures updated GCP, licenses remain on file
  • Comply with reporting of safety related subject discontinuation and safety concerns (AE, SAE or AE of Interest) to the sponsor and IRB/IEC.
  • Autonomously collect, record and report accurate data and demonstrate per FDA guidelines, and review them against the patient's medical record for completeness and accuracy.
  • Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials
  • Manage a monitoring visit including appropriate preparations, support, documentation and follow up. Maintain proper (accurate and timely) communication with the monitor and follow up on all monitor requests
  • Implement a CAPA assessment and follow CAPA related issues through to resolution.
  • Escalates issues of protocol non-compliance to study PI and research department leadership

KPA 3 - Research Financial Practices: Budget/Contract execution and practices research billing compliance
  • Assess a protocol and study plan to develop a study budget.
  • Understanding of the payment terms of the study budget and the and tract items that need to be invoiced for a clinical study.

Position Qualifications/Requirements:
Education:.
  • High school education required
  • Some college required, bachelor's degree preferred and/or Licensed Practical Nurse required

Certifications/Licenses: Previous Experience:
  • 2-5 years prior oncology research/related medical science experience

Core Capabilities:
  • Analysis & Critical Thinking: Critical thinking skills including solid problem solving, analysis, decision-making, planning, time management and organizational skills. Must be detailed oriented with the ability to exercise independent judgment.
  • Interpersonal Effectiveness: Developed interpersonal skills, emotional intelligence, diplomacy, tact, conflict management, delegation skills, and diversity awareness. Ability to work effectively with sensitive and confidential material and sometimes emotionally charged matters.
  • Communication Skills: Good command of the English language. Second language is an asset but not required. Effective communication skills (oral, written, presentation), is an active listener, and effectively provides balanced feedback.
  • Customer Service & Organizational Awareness: Strong customer focus. Ability to build an engaging culture of quality, performance effectiveness and operational excellence through best practices, strong business and political acumen, collaboration and partnerships, as well as a positive employee, physician and community relations.
  • Self-Management: Effectively manages own time, conflicting priorities, self, stress, and professional development. Self-motivated and self-starter with ability work independently with limited supervision. Ability to work remotely effectively as required.
  • Must be able to work effectively in a fast-paced, multi-site environment with demonstrated ability to juggle competing priorities and demands from a variety of stakeholders and sites.
  • Computer Skills:
    • Proficiency in MS Office Word, Excel, Power Point, and Outlook required.
    • Prior experience with electronic medical records (EMR) is preferred
    • Prior experience with clinical trial data entry systems (EDC) preferred
    • Prior Clinical Trial Management Systems (CTMS) preferred.

Travel: 0%
Standard Core Workdays/Hours: Monday to Friday 8:00 AM - 5:00 PM.
#AONC

What American Oncology Network employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom