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Political Data Science Jobs in Indiana (NOW HIRING)

Alexander Chemical Corp

QEC Manager

La Porte, IN · On-site

Performs statistical analysis of data to generate Statistical Process Controls (SPC) and Certified ... Bachelor's degree with emphasis in Chemical Engineering or Quality Control/Environmental Science ...

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Political Data Science information

What are the key skills and qualifications needed to thrive in the Political Data Science position, and why are they important?

To thrive in Political Data Science, you need expertise in statistics, quantitative research methods, and programming (such as Python or R), often supported by a degree in data science, political science, or a related field. Familiarity with data visualization tools like Tableau, statistical software, and experience with databases and big data platforms are typically important, and certifications in data analytics can be an asset. Strong analytical thinking, collaboration, and effective communication skills help you explain complex findings to non-technical stakeholders. These abilities are crucial for providing actionable insights that influence strategic decisions in political campaigns, policy analysis, or governmental organizations.

What are typical daily responsibilities for a Political Data Science professional?

Political Data Science professionals typically spend their days collecting and cleaning large datasets related to voter behavior, public opinion, or legislative trends, and developing statistical models to interpret this information. They collaborate closely with campaign strategists, policy analysts, and communication teams to translate data-driven findings into actionable strategies. Presenting results through visualizations and clear reports is a key part of the job, ensuring that technical insights can influence decisions. The work often involves managing multiple projects simultaneously and adapting quickly to the fast-paced environment of politics and public policy.

What is a Political Data Science job?

A Political Data Science job involves analyzing political data to uncover trends, inform policy decisions, and support political campaigns or organizations. Professionals in this field use statistical modeling, machine learning, and data visualization to interpret voter behavior, public opinion, and legislative patterns. They often work with large datasets from surveys, elections, and social media to provide data-driven insights.

What are the most commonly searched types of Political Data Science jobs in Indiana? The most popular types of Political Data Science jobs in Indiana are:
What are popular job titles related to Political Data Science jobs in Indiana? For Political Data Science jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Political Data Science jobs in Indiana look for? The top searched job categories for Political Data Science jobs in Indiana are:
What cities in Indiana are hiring for Political Data Science jobs? Cities in Indiana with the most Political Data Science job openings:
Political Data Science jobs near you
Infographic showing various Political Data Science job openings in Indiana as of June 2026, with employment types broken down into 50% Full Time, 25% Part Time, and 25% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution.
Clinical Research Coordinator I

Clinical Research Coordinator I

American Oncology Network

Indianapolis, IN • On-site

$19.66 - $34.59/hr

Full-time

Posted yesterday

American Oncology Network rating

6.4

Company rating: 6.4 out of 10

Based on 28 frontline employees who took The Breakroom Quiz

Job description

Location:
Hematology Oncology of Indiana
Pay Range:
$19.66 - $34.59
Job Description Summary
Responsible for the performance of the research study under the medical supervision of the Principal Investigator. The Clinical Research Coordinator I (non-RN) is responsible for the overall successful implementation and ongoing management of the research studies. Ability to perform basics tasks and exhibit the knowledge of key aspects of clinical research at an essential or foundational level
Primary responsibility includes study designs with entry-level complexity (phase 4, observational/registry trial design) and associated study procedures. Administratively and clinically manage an average 5 clinical trials open to accrual annually and/or active (on study treatment) patient volume 2-10 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.
  • Identify and explain key protocol elements and perform study tasks under direct supervision
  • Conduct protocol feasibility assessments and complete feasibility/site assessment questionnaires
  • Identifies and explains inclusion/exclusion criteria and the process of subject identification, prescreening, screening and re-screening
  • Knowledge of the required elements of an informed consent form and the essential elements of the informed consent process.
  • Review of diagnostic tests 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. Document different types of adverse events under direct supervision
  • Ensures proper storage, dispensing, handling and destruction processes for investigational products.
  • Follows process for handling investigational products that have been compromised.

KPA 2 - Regulatory and Data Integrity
  • Follows Institutional Review Board (IRB) / Independent Ethics Committee (IEC) review, approval and reporting requirements for the site. 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.
  • Collect, record and report accurate data and demonstrate per FDA guidelines, and review them against the patient's medical record for completeness and accuracy under direct supervision
  • Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials
  • Prepare documents for monitoring visits under direct supervision. Review visit monitoring follow-up reports / letters and perform requested activities.
  • 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
  • Identifies elements of a study budget as it relates to execution of a protocol.

Position Qualifications/Requirements
Education
  • High school education required
  • Some college is preferred

Previous Experience
  • Prior research or 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.

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