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Lead Scientific Writer Jobs (NOW HIRING)

Houston Methodist

... Lead scientific writing efforts, including manuscripts, abstracts, white papers, and institutional reports Co-lead the design and execution of clinical trials, pragmatic studies, and health system ...

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$40K

$87.4K

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How much do lead scientific writer jobs pay per year?

As of Sep 9, 2026, the average yearly pay for lead scientific writer in the United States is $87,435.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,500.00 and $112,000.00 per year, depending on experience, location, and employer.

What is a lead scientific writer?

Lead Scientific Writers are experienced professionals who oversee the creation, editing, and management of scientific documents such as research articles, grant proposals, regulatory submissions, and technical reports. They often lead a team of writers, ensuring the accuracy, clarity, and consistency of scientific communications. Their role may also involve collaborating with scientists, researchers, and subject matter experts to translate complex scientific data into accessible written materials for various audiences.

How does a lead scientific writer typically collaborate with subject matter experts and project teams?

As a Lead Scientific Writer, you will frequently work alongside subject matter experts, researchers, and multidisciplinary project teams to ensure scientific accuracy and clarity in documentation. This role involves facilitating interviews, reviewing research data, and translating complex scientific concepts into accessible language for various audiences. Effective communication and project management skills are essential, as you often coordinate feedback, manage timelines, and ensure that all materials meet regulatory and publication standards. Regular collaboration helps maintain the integrity and consistency of scientific messaging across multiple projects.

What are the key skills and qualifications needed to thrive as a lead scientific writer, and why are they important?

To thrive as a Lead Scientific Writer, you need advanced scientific knowledge (often with an advanced degree in a life science), excellent writing skills, and experience interpreting complex research data. Familiarity with reference management software, scientific publication platforms, and style guides such as AMA or APA is typically required. Strong project management, attention to detail, and the ability to effectively collaborate with cross-functional teams are essential soft skills. These competencies ensure that scientific content is accurate, accessible, and delivered on time, supporting the credibility and impact of research communications.

What cities are hiring for Lead Scientific Writer jobs?

Cities with the most Lead Scientific Writer job openings:

What states have the most Lead Scientific Writer jobs?

States with the most job openings for Lead Scientific Writer jobs include:

What are popular job titles related to Lead Scientific Writer jobs?

For Lead Scientific Writer jobs, the most frequently searched job titles are:

Infographic showing various Lead Scientific Writer job openings in the United States as of August 2026, with employment types broken down into 89% Full Time, 9% Part Time, and 2% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $87,435 per year, or $42 per hour.

Medical Writer

Pennington, NJ • On-site

Artech Information System LLC
Recruiting and Staffing Services • 10K+ employees
Learn more about Artech Information System LLCexternal

Contractor

Re-posted 22 days ago

Key responsibilities

  • Coordinate and author regulatory documents such as CSRs, CTD summary documents, aggregate safety reports, and risk management plans, ensuring integration of scientific, medical, and regulatory input.

  • Participate in document strategy sessions and manage timelines for all components of assigned documents.

  • Review, edit, and ensure the quality and timely completion of documents while complying with internal and external processes and guidelines.

Job description

Company Description

Artech Information System, a global staffing and IT consulting company. We are constantly on the lookout for professionals to fulfill the staffing needs of our clients and we currently have a job opening that may interest you.

Job Description

Position: Medical Writer

Location: Pennington, New Jersey-08534

Duration: 6 Months

Job Description:

Scientific Writer for Aggregate Reports:

  • Coordinate and author documents needed for regulatory submissions (eg, CSRs, CTD summary documents, aggregate safety reports, risk management plans), ensuring the coordination and integration of the scientific, medical, and regulatory input from cross-functional team members.
  • Participate in relevant document sub team(s) and ensure effective planning and management of timelines for all components of assigned documents.
  • Participate in document strategy sessions, including messaging, document flow, logic, and consistency for assigned projects.
  • Comply with internal and external processes and guidelines while managing the review process and, on an ongoing basis, resolve issues, errors, or inconsistencies with pertinent team members to ensure timely completion and high quality of assigned documents.
  • Review and edit documents as required.
  • Considerable experience in Assignment on Cross Functional Teams would be an advantage.

Qualifications:

  • PhD/MD/PharmD in a relevant scientific discipline or MS / BS with a minimum of 3 years (MS) to 5 years (BS) in pharmaceutical regulatory documentation, or equivalent, and good understanding of requirements for regulatory submission documents. In addition, (i) demonstrated strong writing skills as evidenced by good quality writing in pharmaceutical regulatory documentation and/or publications in peer-reviewed journals, (ii) good understanding of global pharmaceutical drug development and requirements for submission of regulatory dossiers to global health authorities, (iii) demonstrated ability to manage timelines and quality of work using strong organizational, communication, facilitation and interpersonal skills in a cross-functional team, (iv) working knowledge of a document management system and basic knowledge of document publishing process, (v) analyzed and interpreted complex data from a broad range of scientific disciplines.Coordinate and author regulatory documents (e.g. phase I/II clinical study reports, Investigator's Brochure) ensuring the coordination and integration of the scientific, medical and regulatory input from development team members.2. When assigned as Lead Writer, ability to lead other writers, including developing strategies/ plans and managing projects, in order to complete multiple documents for regulatory submissions.3. Demonstrate mastery of complex writing assignments (e.g., Phase III CSRs, CSS, CSE, Background Packages, etc.) across therapeutic areas or multiple projects.4. Participate in relevant filing subteam(s) and ensure effective planning and management of timelines for all components of assigned documents.5. Lead or co-lead (with Doc Lead) teams to define content and data displays for CSR prototypes and shells. 6. Able to collaborate with project team to respond to health authority questions, requests, etc.7. Provide departmental management with adequate information to help assess resource needs.
Additional Information

All your information will be kept confidential according to EEO guidelines.

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About Artech

Sourced by ZipRecruiter

Artech is a leading IT staffing and consulting company based in Morristown, NJ, US. Since its foundation in 1992, Artech has mastered in complementing human expertise with technology and business acumen to produce world-class staffing solutions. The company caters to diverse industry sectors, including financial services, healthcare, telecommunication, energy and utilities, supply chain, and retail. It provides IT consulting, project management, professional and staff augmentation, and managed staffing services. Artech's mission is to provide exceptional IT staffing services to its clients by comprehending their business needs and then crafting a customized staffing strategy. Its notable achievement includes being recognized as one of the largest IT staffing companies in the U.S, according to Staffing Industry Analysts (SIA).

Industry

Recruiting and staffing services

Company size

10,000+ Employees

Headquarters location

Morristown, NJ, US

Year founded

1992

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