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Part Time Library Data Entry Jobs in Arizona (NOW HIRING)

Charter One is currently accepting applications for a Part-Time HR File Clerk who will work at our ... Performs HRIS data entry * Other duties as assigned Minimum qualifications: * Detail-oriented and ...

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PART-TIME LAW FIRM RECEPTIONIST/FILE CLERK, Monday through Friday, 1:00 pm to 5:00 pm for busy ... Administrative support: Assist with filing, data entry, and other administrative tasks as needed.

Part-Time Court Clerk

Fountain Hills, AZ ยท On-site

$23.34 - $33.38/hr

Fountain Hills, AZ Job Type: Part-time Job Number: PTCourtClerk2026 Department: Municipal Court ... Performs a variety of data entry into the case management system, including citation entry, case ...

APPAREL/CLERK

Phoenix, AZ ยท On-site

$14.25 - $19.25/hr

Whether you're seeking a part-time position or a new career path, we've got a fresh opportunity for you. Apply today to become part of our Fry's family! What you'll receive from us: The Kroger Family ...

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Part Time Library Data Entry information

What are the key skills and qualifications needed to thrive as a Part Time Library Data Entry Clerk, and why are they important?

To thrive as a Part Time Library Data Entry Clerk, you need strong attention to detail, accurate typing skills, and basic computer literacy, often supported by a high school diploma or equivalent. Familiarity with library cataloging software, data management systems, and spreadsheets like Microsoft Excel is typically required. Organizational skills, dependability, and the ability to work independently make someone stand out in this position. These skills ensure accurate and efficient data management, helping maintain the quality and accessibility of library records.

What jobs pay $400 an hour?

Part time library data entry jobs typically do not pay $400 an hour, as such high rates are uncommon for entry-level or administrative roles. High-paying jobs at this level are usually specialized professions requiring advanced skills, certifications, or extensive experience, such as consulting, legal, or medical roles. For most part time data entry positions, wages are significantly lower and depend on the employer and location.

What are part time library data entry jobs?

Part time library data entry jobs involve entering, updating, and maintaining library records and databases. Employees in these roles typically input information about books, periodicals, and other library materials, ensuring that catalogues are accurate and up to date. They may also assist with digitizing records, checking data for errors, and supporting other administrative tasks. These positions often require attention to detail, basic computer skills, and the ability to work independently for a set number of hours each week.

Can you get hired at a library with no experience?

Part-time library data entry positions often do not require prior experience, as they mainly involve basic computer skills and attention to detail. Employers may provide on-the-job training, and having familiarity with library software or data management tools can be helpful. Entry-level roles are accessible to those new to the field.

Can I work a data entry job with no experience?

Part time library data entry jobs typically do not require prior experience, as training is often provided. Basic skills such as typing accuracy, attention to detail, and familiarity with spreadsheet or database software are usually sufficient to start. Employers may prefer candidates with some computer skills, but many entry-level positions are accessible to beginners.

Is AI replacing librarians?

AI is not replacing librarians, especially in roles like part-time library data entry, where human oversight is essential for accuracy and context. AI tools can assist with tasks such as cataloging and data management, but librarians' expertise in information organization, customer service, and community engagement remains vital. The job typically requires attention to detail and familiarity with library systems and software.

What are some common challenges faced in a part-time library data entry role, and how can they be managed?

A common challenge in a part-time library data entry position is maintaining accuracy while handling large volumes of cataloging or circulation data within tight timeframes. To manage this, it's helpful to develop strong attention to detail and establish a routine for double-checking entries. Additionally, learning the library's cataloging software and understanding classification systems can streamline the workflow and reduce errors. Working closely with librarians and other staff for clarification can also help resolve uncertainties quickly and keep records consistent.

What is the difference between Part Time Library Data Entry vs Part Time Library Clerk?

AspectPart Time Library Data EntryPart Time Library Clerk
CredentialsBasic computer skills, data entry experienceHigh school diploma or equivalent, customer service skills
Work EnvironmentOffice or library setting, focused on data inputPublic library, interacting with visitors and managing collections
Employer & Industry UsageLibraries, educational institutions, data management companiesPublic and academic libraries, community centers
Common Search & Comparison IntentUnderstanding data entry roles in librariesCustomer service and library assistance roles

Part Time Library Data Entry primarily involves inputting and managing library data, requiring strong computer skills. In contrast, Part Time Library Clerk focuses on assisting visitors, managing library materials, and providing customer service. Both roles are essential in library operations but differ in responsibilities and skill requirements.

What job categories do people searching Part Time Library Data Entry jobs in Arizona look for? The top searched job categories for Part Time Library Data Entry jobs in Arizona are:
Infographic showing various Part Time Library Data Entry job openings in Arizona as of June 2026, with employment types broken down into 100% Part Time. Highlights an 60% In-person, and 40% Remote job distribution.
Clinical Research Associate - Part Time

Clinical Research Associate - Part Time

CND Life Sciences

Scottsdale, AZ โ€ข On-site

$36.54/hr

Part-time

Posted yesterday


Job description

Description
The Clinical Research Associate (CRA) is responsible for overseeing and monitoring clinical trials conducted at CND's internal site and investigator sites sponsored by CND or in collaboration with external partners. This role ensures that studies are executed in compliance with study protocols, Good Clinical Practice (GCP) guidelines, budget constraints, and established milestone timelines. The CRA must have a strong understanding of clinical trial methodologies, regulatory requirements, and the ability to collaborate effectively with the investigators and internal and external cross-functional teams. The CRA consistently upholds the highest standards of professionalism.
Job Responsibilities
  • Regulatory Compliance: Ensure all clinical trials are conducted in adherence to the study protocol, ICH-GCP guidelines, relevant regulations and SOPs. Manage central IRB tasks for participating sites from start-up through close-out.
  • CND Site Subject Visits: Assist providers with subject recruitment, scheduling and conducting site visits at the internal CND site as needed. Responsibilities may include obtaining informed consent (ICF), assessing inclusion/exclusion criteria, recording vitals, and performing blood draws.
  • Site Initiation: Conduct site initiation visits remotely or in person to assess site readiness, including regulatory start-up, facility reviews, annual bio-calibrations, supply storage, staff qualifications and training, study procedures and data entry management. Ensure all required site documents are collected and tracked in compliance with regulatory requirements and internal Standard Operating Procedures (SOPs). May also involve updating clinicaltrials.gov with site-specific information.
  • Study Monitoring: Perform regular site monitoring visits remotely (via eCRF) or in person (via site source documents) per study-specific monitoring plans and timelines. Oversee data entry, protocol adherence, query resolution, quality compliance, and patient safety reporting, escalating protocol deviations or subject safety concerns as needed. Assist in the development of study-specific monitoring plans.
  • Site Communication: Maintain proactive communication with site staff, responding to inquiries timely and escalating urgent matters as necessary.
  • Site Engagement and Subject Recruitment: Monitoring weekly site recruitment logs to verify subject eligibility and enrollment. Assist sites with IRB approvals for advertising and recruitment strategies. Support community patient advocacy outreach when needed.
  • Site Invoices: Review and approve site invoices based on completed EDC data entry and query resolution for all subject visits invoiced, including start-up and close-out visits.
  • Data Management: Oversee the collection, processing, and documentation of study data. Ensure data integrity through thorough data review and timely query resolution following study-specific monitoring plan milestones.
  • Safety Reporting: Oversee the reporting of adverse events and serious adverse events, ensuring compliance with regulatory requirements.
  • Site Close-Out: Conduct site close-out activities to ensure proper data lock, storage, and archiving study documents.
  • Trial Documentation: Maintain and manage all clinical trial documents, ensuring they remain current and compliant with regulatory standards.
  • Team Collaboration: Work closely with internal and external cross-functional teams and vendors to ensure clinical trials are executed efficiently, within budget and in alignment with study milestones.
  • Reporting: Provide regular updates and comprehensive reports to the Senior Director of Clinical Research and/or designated CR lead and other stakeholders on trial progress.
  • Quality Assurance and Compliance Participate in internal and external audits, addressing findings, and implement corrective and preventive actions as necessary.
  • Perform other duties as assigned.

Knowledge, Skills & Experience
  • Minimum of 5 years of clinical research experience as a Clinical Research Coordinator or at least 2 years of experience as a Clinical Research Associate.
  • Therapeutic experience in neurology is highly preferred.
  • Experience in Phase I, II or III of clinical trials; familiarity with NIH and other government-sponsored protocols a plus.
  • In-depth knowledge of ICH-GCP guidelines and relevant regulatory requirements for clinical trial conduct.
  • Strong proficiency in IT tools including the MS 365 suite, Electronic Data Capture (EDC) systems, Clinical Trial Management Systems (CTMS) and other applicable technologies.
  • Excellent written and verbal communication skills.
  • Strong multitasking skills, attention to detail, creative problem-solving, and the ability to maintain accurate records.
  • Demonstratedability to identify and resolve site-related challenges with strong negotiation skills.
  • Proven ability to work effectively in a team-based environment

Education, Certifications, and Licensures
  • Bachelor's of Science degree or related field required.
  • The Collaborative Institutional Training Initiative (CITI) Good Clinical Practice (GCP) certification, or its equivalent, or willing to complete within first month of hire.
  • International Air Transport Association (IATA) certification, if indicated

Other
  • Combination of seated and standing work to complete the core functions of the role
  • Sit and stand for long periods of time
  • Visual acuity and analytical skills
  • This job will be expected to work onsite at CND's Scottsdale, AZ headquarters 3-5 days/week