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Weekend Document Review Jobs in Madison, WI (NOW HIRING)

Summit BHC

RN/FT/AM - Weekend Only

Middleton, WI · On-site

... and documents appropriately; transcribes and reviews physician's orders. Ensures physician's orders are legible if taken verbally and transcribed appropriately per policy and procedure. • ...

TekWissen LLC

Documentation Specialist

Madison, WI · On-site

$20 - $25/hr

Position: Documentation Specialist Location: Madison, WI, 53711 Duration: 12 Months Job Type: Part Time Work Type: Onsite Responsibilities * Manage parts setup in SAP to support new launches ...

O'Leary Dental Office

Dental hygienist

Janesville, WI · On-site

$40 - $55/hr

Part-Time Hygienist - flexible hours, no Fridays or weekends Established general dental practice ... reviewing medical histories. Utilize EMR systems for accurate documentation of patient records and ...

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Weekend Document Review information

See Madison, WI salary details

$14

$23

$33

How much do weekend document review jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for weekend document review in Madison, WI is $23.51, according to ZipRecruiter salary data. Most workers in this role earn between $19.86 and $27.12 per hour, depending on experience, location, and employer.

What is a weekend document review?

A Weekend Document Review job involves reviewing legal documents, typically for law firms or legal service providers, to identify relevant information for litigation or regulatory matters. Attorneys in these roles analyze documents for privilege, confidentiality, and relevance using specific review platforms. These projects often occur on a temporary basis and are ideal for legal professionals seeking flexible or additional work. Weekend shifts allow firms to meet tight deadlines and manage large volumes of documents efficiently.

What are the typical responsibilities and workflow for a weekend document review?

As a Weekend Document Review professional, you are primarily responsible for reviewing large volumes of legal documents to assess relevancy, privilege, and confidentiality based on case guidelines. You will typically work on secure platforms, closely following instructions provided by case managers or supervising attorneys. The workflow often involves meeting weekly milestones, flagging issues, and collaboratively discussing findings with other reviewers or team leads. While the schedule is focused on weekends, you may work independently or with a remote team to ensure project deadlines are met. This structure provides flexibility while still contributing significantly to ongoing legal matters.

What are the key skills and qualifications needed to thrive in the weekend document review position, and why are they important?

To thrive as a Weekend Document Review professional, you need a solid understanding of legal concepts, attention to detail, and strong analytical skills, typically supported by a JD or relevant paralegal certification. Proficiency with document review platforms such as Relativity or Concordance, along with experience using e-discovery tools, is highly valued. Strong organizational skills, effective communication, and the ability to work independently or within a team set top performers apart. These skills and qualities are essential to ensure accurate document analysis, timely completion of review projects, and optimal support for legal teams during critical case preparations.

What are popular job titles related to Weekend Document Review jobs in Madison, WI?

For Weekend Document Review jobs in Madison, WI, the most frequently searched job titles are:

What job categories do people searching Weekend Document Review jobs in Madison, WI look for?

The top searched job categories for Weekend Document Review jobs in Madison, WI are:

Weekend Document Review jobs near you
Infographic showing various Weekend Document Review job openings in Madison, WI as of August 2026, with employment types broken down into 75% Full Time, 7% Part Time, 4% Temporary, 10% Contract, and 4% Nights. Highlights an 83% In-person, 5% Hybrid, and 12% Remote job distribution, with an average salary of $48,899 per year, or $23.5 per hour.

Quality Specialist III, Document Control and Training

Arrowhead Pharmaceuticals

Verona, WI • On-site

$78K - $98K/yr

Full-time

Posted 3 days ago

New

Job description

Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.
The Position
Serve as an individual contributor supporting the day-to-day execution of controlled documentation and training compliance activities within the Quality Assurance function. Process and maintain controlled documents, quality records, and training records within the eQMS and learning management system, ensuring accuracy, completeness, and compliance with applicable regulatory requirements. Support the issuance, reconciliation, and review of applicable controlled documents to ensure traceability of applicable GxP documentation.
Responsibilities
Document Control and Records Management
  • Support document formatting, metadata entry, routing, approval workflows, effective date coordination, periodic review activities, and controlled document lifecycle maintenance.
  • Support issuance, reconciliation, and review of controlled documents and completed records to verify completeness and compliance with GDocP requirements.
  • Maintain organized and audit-ready document control files, including effective documents, superseded or obsolete records, document change records, and supporting documentation.
  • Support preparation and organization of document control packages for internal audits, client audits, regulatory inspections, and document change control activities.
  • Assist with controlled copy management, document distribution, retrieval, archival, and record retention activities, as applicable.
  • Assist with the development, revision, and maintenance of document control work instructions and SOPs, as directed.
  • Support formatting and routing of corporate policies through approval workflows, and coordinate periodic review timing with Legal, Health Care Compliance, IS&I and applicable stakeholders.
  • Perform additional duties as assigned.

Training Administration and Compliance
  • Monitor training completion rates, identify at-risk or past-due training items, and proactively escalate concerns, as applicable.
  • Assist in developing and updating training materials, including slide decks, assessments, and Read-and-Understand documents for GxP and SOP-based training programs.
  • Support new hire orientation and classroom training activities.
  • Compile and organize training completion data and generate routine compliance reports for review by management.
  • Maintain training records in an organized, accurate, and audit-ready state.
  • Perform additional duties as assigned.

Requirements
  • BS/BA in an applicable scientific field such as chemistry, biology, or biochemistry
  • Minimum of 5 years of experience in a pharmaceutical/biotech company, contract manufacturing organization or contract research organization writing and maintaining documents.
  • Ability to follow company procedures, work instructions, and policies.
  • Ability to multi-task and prioritize work with minimal supervision.
  • Excellent interpersonal, verbal, and written communication skills.
  • Strong organizational skills with the ability to manage multiple tasks, prioritize workload, and meet competing deadlines.

Preferred
  • Experience with an eQMS/eDMS platform (e.g., Veeva) and/or LMS software in a GxP-regulated environment.
  • Working knowledge of GMP, GCP, and/or GLP regulations.
  • Competent knowledge of, and ability to use, Adobe Acrobat, Microsoft Word, PowerPoint and Excel.

Wisconsin pay range
$78,000-$98,000 USD
Arrowhead provides competitive salaries and an excellent benefit package.
Candidates must have current, valid authorization to work in the country where this role is located.
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