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Contract Proofreader Jobs in Boston, MA (NOW HIRING)

Clinical Trial Associate

Boston, MA · On-site

$86K - $100K/yr

Manages study investigator CDAs, contract approval and purchase order creation. * Coordinates cross ... Requires strong attention to detail in composing and proofing materials, establishing priorities ...

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Contract Proofreader information

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How much do contract proofreader jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for contract proofreader in Boston, MA is $30.04, according to ZipRecruiter salary data. Most workers in this role earn between $22.21 and $36.54 per hour, depending on experience, location, and employer.

What is a contract proofreader?

A Contract Proofreader is a freelance or temporary professional who reviews written content for grammar, spelling, punctuation, and formatting errors. They ensure accuracy and consistency in various types of documents, such as articles, reports, marketing materials, or legal papers. Contract Proofreaders typically work on a project basis for businesses, publishers, or individuals, providing their services remotely or onsite as needed. This role requires strong attention to detail, language proficiency, and familiarity with style guides like AP, Chicago, or MLA.

What are the key skills and qualifications needed to thrive as a contract proofreader?

To thrive as a Contract Proofreader, you need exceptional grammar, spelling, and punctuation skills, along with a keen attention to detail and a solid understanding of style guides such as AP or Chicago Manual of Style. Familiarity with editing and proofreading tools like Microsoft Word's Track Changes, Adobe Acrobat, and online platforms such as Grammarly is often required. Strong time management, reliability, and the ability to communicate clearly with clients or project managers are standout soft skills. These qualities ensure error-free content, efficient workflow, and successful collaboration in fast-paced, contract-based environments.

What are the typical challenges faced by contract proofreaders and how can they be managed?

Contract Proofreaders often face tight deadlines, a high volume of content, and the need to quickly adapt to varied editorial styles across different clients. Managing these challenges requires strong organizational skills, the ability to prioritize multiple assignments, and maintaining effective communication with clients to clarify expectations or resolve ambiguities. Building a reliable workflow—such as setting aside distraction-free time for careful review—can help minimize errors. Proactively staying updated on industry trends and style guide updates also supports consistent quality and client satisfaction.

What are the most commonly searched types of Proofreader jobs in Boston, MA?

The most popular types of Proofreader jobs in Boston, MA are:

What are popular job titles related to Contract Proofreader jobs in Boston, MA?

For Contract Proofreader jobs in Boston, MA, the most frequently searched job titles are:

What cities near Boston, MA are hiring for Contract Proofreader jobs?

Cities near Boston, MA with the most Contract Proofreader job openings:

Infographic showing various Contract Proofreader job openings in Boston, MA as of August 2026, with employment types broken down into 86% Full Time, 5% Part Time, 2% Temporary, and 7% Contract. Highlights an 86% Physical, 6% Hybrid, and 8% Remote job distribution, with an average salary of $62,489 per year, or $30 per hour.

Clinical Trial Associate

Verastem

Boston, MA • On-site

$86K - $100K/yr

Full-time

Re-posted 25 days ago


Job description

Company Profile:
At Verastem Oncology, we address urgent needs of patients living with cancers driven by RAS/MAPK pathway mutations, a key driver of tumor growth and treatment resistance. FDA approval of AVMAPKI FAKZYNJA CO-PACK delivered the first therapy for women living with recurrent KRAS-mutated low-grade serous ovarian cancer, a rare cancer with significant unmet need. We've launched this novel/novel combination therapy in the U.S. and are exploring pathways for Europe and Japan. We continue to advance our pipeline of drugs to help block cancer cell survival, inhibit tumor growth, and overcome treatment resistance. This is an exciting opportunity to shape the future of cancer care and make a meaningful impact in the lives of patients.
Summary:
Responsible for assisting and providing support to the members of the clinical operations project team to facilitate the operational execution of the clinical trial processes in accordance with regulatory guidelines and ICH/GCP standards.
Responsibilities:
  • Manages trial related documents in the Veeva Vault Trial Master File (TMF); manages user access and facilitate training for internal/external users as needed; trains new users.
  • Uploads and reviews TMF documents for completeness, accuracy and compliance with protocol and applicable regulations, standard operating procedures and best practices.
  • Performs quality checks and follow-up on resolution of open issues to ensure cross functional study team members are compliant with use of required documents within the TMF.
  • Audits TMFs and resolves discrepancies with minimal supervision.
  • Creates and maintains internal folders on company share drive(s).
  • Manages study investigator CDAs, contract approval and purchase order creation.
  • Coordinates cross function project team meetings with Clinical Project Manager and assists in preparation of agendas, minutes and tracking of action items.
  • Assists in the creation of study materials, including but not limited to documents, presentations and reports.
  • Supports CPM to established and maintain the tracking tools for project metrics such as site activation, patient enrollment and site contacts.
  • Reviews and assists in the collection of essential documents for completeness and compliance with SOPs, the protocol and appropriate regulations.
  • Creates and reviews IMP release packet prior to initiation; review background information of potential new sites (e.g. debarment check, Inspection history, etc).
  • Assists study team and sites with preparation for audits/inspections.
  • Participates in inter-departmental workgroups to create or enhance processes.
  • May participate in the training of CRO teams, investigators and study team members.
  • May serve as the point of contact for vendors and oversee selected vendor activities.
  • May be responsible for updating Clintrials.gov.
  • Performs administrative tasks to support team members with clinical trial execution, as needed.

Qualifications:
  • Bachelor's degree or nursing degree is required. Scientific/health care field preferred, but not required.
  • Minimum of 4 years' experience in relevant field (e.g. clinical site, CRO, Sponsor or clinical trial vendor).
  • Relevant experience in clinical research or related field.
  • Adequate Good Clinical Practice training.
  • General knowledge of guidelines governing clinical research.
  • Comfortable with technology and ability to learn new systems quickly.
  • Experienced with Veeva TMF.
  • Strong knowledge of MS Word, Excel, PowerPoint and Outlook.
  • Requires strong attention to detail in composing and proofing materials, establishing priorities, scheduling and meeting deadlines.
  • Must be able to professionally interact and communicate with visitors, vendors and individuals at all levels of the organization.
  • Must be able to work in a fast-paced environment with demonstrated ability to work on multiple competing tasks and demands.
  • Ability to work successfully within a cross-functional team.

The base salary range (86K-100K) provided reflects our current estimate of what we anticipate paying for this position. Your actual base salary will be based on several factors, including job-related skills, experience, internal equity, relevant education or training, location, and market dynamics. In addition, you will be eligible for an annual bonus, equity compensation, and a competitive benefits package.