ZipRecruiter

Log In

2

Remote Document Review Jobs in Worcester, MA (NOW HIRING)

Sigma Systems, Inc.

Medical Writer

Marlborough, MA · Remote

... Remote Medical Writer The Medical Writer is responsible for authoring, reviewing, and coordinating the development of high-quality clinical and regulatory documents that support global clinical ...

BerryDunn

Proposal Coordinator

Waltham, MA · On-site +1

$26 - $30/hr

This position may be based in Portland, Maine, one of our other office locations, or remote in ... document review features. * Familiarity with leveraging AI tools to improve productivity ...

Beacon Talent

Remote Psychiatrist

Worcester, MA · Remote

$150 - $200/hr

Location: Remote (United States) Type: 1099 Independent Contractor, Part-Time or Full-Time ... Document within our behavioral health EMR to the standard required for payer review * Escalate ...

Beacon Talent

Remote Psychiatrist

Littleton, MA · Remote

$150 - $200/hr

Location: Remote (United States) Type: 1099 Independent Contractor, Part-Time or Full-Time ... Document within our behavioral health EMR to the standard required for payer review * Escalate ...

Dutch

Virtual Care Veterinarian (Remote)

Woonsocket, RI · Remote

$50 - $80/hr

Review medical history, symptoms, and treatment concerns shared through Dutch's digital platform ... Document all encounters thoroughly using Dutch's EMR * Collaborate with Dutch's clinical leadership ...

micro1 AI

Physics Modeling Expert - Remote

Worcester, MA · Remote

$80 - $140/hr

Solve advanced physics problems from your specialization, delivering rigorous, well-documented ... Iterate on submitted solutions in response to feedback from project reviewers, ensuring corrections ...

VIVA USA INC

Clinical Pharmacist Advisor

Woonsocket, RI · On-site +1

$113K - $135K/yr

Remote Description: Position Summary As a Clinical Pharmacist Advisor, Medicare B Operations, you ... Accurately set up cases, review documentation, and apply work instructions to ensure correct and ...

next page

Showing results 1-20

All JobsDocument Review JobsRemote Document Review JobsRemote Document Review Jobs in Worcester, MA

Remote Document Review information

See Worcester, MA salary details

$13

$23

$33

How much do remote document review jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for remote document review in Worcester, MA is $23.33, according to ZipRecruiter salary data. Most workers in this role earn between $19.71 and $26.92 per hour, depending on experience, location, and employer.

What is remote document review?

Remote document review is a legal process where attorneys or contract professionals examine and analyze documents electronically from remote locations, rather than in a traditional office setting. This work is often done for litigation, investigations, or regulatory compliance, and involves identifying relevant, privileged, or confidential information within large sets of electronic files. Advances in secure technology allow reviewers to access, review, and tag documents using specialized software, all while maintaining data security and client confidentiality. Remote document review offers flexibility for workers and law firms, as well as cost savings on office space and resources.

What are remote document review jobs?

In a remote document review job, you focus on verifying the accuracy and completion of important documents, typically while working from home or another remote location. The most common job in this field is that of remote document review attorney because most documents that need verification are legal documents, such as contracts and court filings. As part of the service you provide for a company, you may also offer legal advice when something on a document is incorrect, explain which documents are likely to be needed for a particular project, and act as a second pair of eyes for content already reviewed by an attorney. Outside of legal jobs, most remote document review roles entail duties like filing for contracts with the federal government or translating material that companies do not want to rely on one translator to review.

What are the key skills and qualifications needed to thrive as a remote document review professional, and why are they important?

To thrive as a Remote Document Review professional, you need strong analytical skills, attention to detail, and a background in law—often requiring a JD degree or paralegal certification. Familiarity with e-discovery platforms such as Relativity or Concordance, as well as secure file-sharing systems, is typically expected. Excellent time management, effective written communication, and the ability to work independently are standout soft skills. These competencies ensure accurate, efficient review of legal documents while maintaining confidentiality and meeting tight deadlines.

What are some common challenges faced in remote document review roles, and how can they be managed effectively?

Remote document review professionals often face challenges such as maintaining focus during repetitive tasks, meeting strict deadlines, and navigating communication barriers with team members. To manage these effectively, it's important to set up a distraction-free workspace, leverage organizational tools to track progress, and proactively communicate with project managers and peers about any questions or issues. Utilizing secure collaboration platforms and regularly scheduled check-ins can also help keep the review process efficient and aligned with team goals.

What is the difference between Remote Document Review vs Remote Data Entry?

AspectRemote Document ReviewRemote Data Entry
Required CredentialsHigh school diploma or equivalent; some roles may require legal or industry-specific certificationsHigh school diploma or equivalent; basic computer skills often sufficient
Work EnvironmentHome-based, often part of legal, healthcare, or compliance teamsHome-based, typically in administrative or data management departments
Employer & Industry UsageLegal firms, healthcare providers, insurance companiesBusinesses across various sectors including healthcare, finance, and retail

Remote Document Review involves analyzing and evaluating documents for legal, compliance, or industry-specific purposes, requiring attention to detail and sometimes specialized knowledge. Remote Data Entry focuses on inputting or updating data into systems, emphasizing accuracy and speed. While both roles are remote and require basic computer skills, they serve different functions within organizations.

More about Remote Document Review jobs

What are popular job titles related to Remote Document Review jobs in Worcester, MA?

For Remote Document Review jobs in Worcester, MA, the most frequently searched job titles are:

What job categories do people searching Remote Document Review jobs in Worcester, MA look for?

The top searched job categories for Remote Document Review jobs in Worcester, MA are:

What cities near Worcester, MA are hiring for Remote Document Review jobs?

Cities near Worcester, MA with the most Remote Document Review job openings:

Remote Document Review jobs near you
Infographic showing various Remote Document Review job openings in Worcester, MA as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $48,529 per year, or $23.3 per hour.

Medical Writer

Sigma Systems, Inc.

Marlborough, MA • Remote

Contractor

Posted 4 days ago

Job description

37554294 Remote Medical Writer, 7 Months Contract
Sigma Systems is currently looking for a Remote Medical Writer
The Medical Writer is responsible for authoring, reviewing, and coordinating the development of high-quality clinical and regulatory documents that support global clinical development programs. This role works closely with cross-functional stakeholders to ensure documents are scientifically accurate, strategically aligned, and delivered according to established timelines and medical writing plans

Responsibilities:

  • Author, edit, and review clinical and regulatory documents, including:
    • Clinical study protocols and protocol amendments
    • Investigator Brochures (IBs)
    • Clinical Study Reports (CSRs)
    • Briefing Book support
    • IND and NDA summary documents and other regulatory submission materials
  • Develop documents that are consistent with regulatory requirements, internal standards, and medical writing plans, while supporting the overall clinical development lifecycle and program objectives for one or more clinical development programs.
  • Collaborate with cross-functional teams, including Clinical Development, Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, Pharmacovigilance, and Medical Affairs, to gather, interpret, and integrate scientific and clinical information into clear, accurate, and submission-ready documents.
  • Negotiate document deliverable milestones and timelines with cross-functional teams to ensure alignment across functions and adherence to medical writing plans and program objectives.
  • Facilitate document review cycles, resolve reviewer comments, and drive consensus among stakeholders while maintaining quality and schedule commitments.
  • Ensure documentation complies with applicable regulatory guidance, Good Clinical Practice (GCP), company standards, and industry best practices.
  • Contribute to the development and continuous improvement of medical writing processes, templates, style guides, and operational procedures.
  • Support regulatory submissions, health authority interactions, and inspection readiness activities as needed

Core Competencies

  • Scientific and regulatory writing expertise
  • Project and timeline management
  • Cross-functional collaboration and influence
  • Strategic thinking and problem solving
  • Attention to quality and regulatory compliance
  • Effective communication and stakeholder management

Requirements:

  • Advanced degree Bachelor's degree or more.
  • Experience authoring clinical and regulatory documents within the pharmaceutical, biotechnology, or clinical research industry.
  • Strong knowledge of clinical development, regulatory requirements, and applicable guidance documents (e.g., ICH guidelines).
  • Excellent scientific writing, editing, and communication skills.
  • Demonstrated ability to manage multiple projects and negotiate timelines in a cross-functional environment.

Strong organizational skills, attention to detail, and ability to work independently and collaboratively