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Remote Senior Science Writer Jobs in Atco, NJ (NOW HIRING)

Elsevier

Senior Business Analyst I

Philadelphia, PA · On-site +1

$93K - $148K/yr

... scientific evidence Responsibilities * Contributing to the development of new tools, standard ... Working between remote development teams, internal IT and business to ensure requirements are being ...

RELX

Senior Business Analyst I

Philadelphia, PA · On-site +1

$93K - $148K/yr

... scientific evidence Responsibilities * Contributing to the development of new tools, standard ... Working between remote development teams, internal IT and business to ensure requirements are being ...

Iridium Satellite, LLC

Senior Software Developer

Philadelphia, PA · On-site +1

$55 - $72.75/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... militaries, scientific researchers, and lone workers, as well as ships, aircraft and remote ... Excellent written and verbal communication skills, with the ability to clearly articulate products ...

Iridium Satellite, LLC

Senior Software Developer

Philadelphia, PA · On-site +1

$55 - $72.75/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... militaries, scientific researchers, and lone workers, as well as ships, aircraft and remote ... Excellent written and verbal communication skills, with the ability to clearly articulate products ...

Truvani

Direct Response Copywriter - REMOTE

Philadelphia, PA · On-site +1

$75K - $105K/yr

  • Medical

  • Retirement

  • PTO

Senior Creative Strategist, Performance Advertising Compensation: $75,000-$105,000 base, based on ... Write ad copy, hooks, scripts, and creative briefs for Meta, YouTube, and other paid channels ...

Truvani

Direct Response Copywriter - REMOTE

Philadelphia, PA · Remote

$75K - $105K/yr

  • Medical

  • Retirement

  • PTO

Senior Creative Strategist, Performance Advertising Compensation: $75,000-$105,000 base, based on ... Write ad copy, hooks, scripts, and creative briefs for Meta, YouTube, and other paid channels ...

Truvani

Direct Response Copywriter - REMOTE

Philadelphia, PA · Remote

$75K - $105K/yr

  • Medical

  • Retirement

  • PTO

Senior Creative Strategist, Performance Advertising Compensation: $75,000-$105,000 base, based on ... Write ad copy, hooks, scripts, and creative briefs for Meta, YouTube, and other paid channels ...

Wood Plc

Senior Process Engineer

Philadelphia, PA · On-site +1

$104K - $135K/yr

Overview / Responsibilities Senior Process Engineer (Life Sciences) Wood is currently seeking a ... Excellent oral and written communication skills, decision making capabilities, problem resolution ...

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All JobsScience Writer JobsRemote Senior Science Writer JobsRemote Senior Science Writer Jobs in Atco, NJ

Remote Senior Science Writer information

See Atco, NJ salary details

$30.3K

$92K

$169.9K

How much do remote senior science writer jobs pay per year?

As of Aug 18, 2026, the average yearly pay for remote senior science writer in Atco, NJ is $91,968.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,500.00 and $100,400.00 per year, depending on experience, location, and employer.

What does a remote senior science writer do?

A Remote Senior Science Writer is responsible for creating, editing, and reviewing scientific content for a variety of audiences, such as academic journals, research institutions, or the general public, all while working from a remote location. They translate complex scientific concepts into clear, accurate, and engaging materials like articles, reports, white papers, or grant proposals. Senior Science Writers often collaborate with researchers, subject matter experts, and editors to ensure scientific accuracy and accessibility. Their role may also involve mentoring junior writers, managing projects, and staying updated on the latest developments in science and science communication.

What are some common challenges faced by remote senior science writers when collaborating with global research teams?

Remote Senior Science Writers often work with international research teams, which can present challenges such as navigating time zone differences, ensuring clear communication despite cultural and language barriers, and managing multiple collaborative platforms. To succeed, writers need to be proactive in scheduling meetings, use collaborative tools effectively, and maintain organized documentation of revisions and feedback. Building strong relationships with team members and setting clear expectations for project timelines can help streamline the writing and review process.

What are the key skills and qualifications needed to thrive as a remote senior science writer, and why are they important?

To thrive as a Remote Senior Science Writer, you need advanced writing and editing skills, a strong background in science (often at least a bachelor’s or master’s degree), and experience translating complex scientific concepts for diverse audiences. Familiarity with reference management software, content management systems (CMS), and proficiency with collaborative tools like Google Workspace are typically required. Outstanding attention to detail, time management, and the ability to communicate clearly with both subject-matter experts and non-experts are crucial soft skills. These competencies ensure clear, accurate, and engaging science communication that meets publication standards and client needs in a remote work environment.
Remote Senior Science Writer jobs near you

Senior Biostatistician (Remote Status)

American Association for Cancer Research

Philadelphia, PA • On-site, Remote

Full-time

Re-posted 12 days ago

Job description

Overview
The American Association for Cancer Research (AACR), with more than 61,000 laboratory, translational, and clinical researchers; population scientists; other health care professionals; and patient advocates residing in 143 countries and territories around the world, is the first and largest organization in the world dedicated to advances in all areas of high-quality, innovative cancer research. Its mission is to prevent and cure all cancers. The programs and activities of the AACR foster the exchange of new knowledge among scientists and physicians in cancer research as well as in related sciences. The AACR publishes ten peer-reviewed scientific journals and an award-winning magazine for cancer patients and their loved ones; convenes topical scientific conferences and an annual meeting that draws more than 22,500 participants; offers educational workshops that train young investigators in a variety of scientific and clinical areas; funds research fellowships, career development awards, and research grants for both senior and junior investigators; raises public awareness of the progress in the biology, detection, diagnosis, treatment, and prevention of cancer; engages actively in advocacy for increased federal research funding and other national policies that accelerate progress against cancer; and interacts with regulatory agencies to support regulatory science and policy. Learn more at www.aacr.org.
About the Project
AACR Project Genomics, Evidence, Neoplasia, Information, Exchange (GENIE) is a publicly accessible international cancer registry of real-world clinico-genomic data assembled through data sharing between 20 of the leading cancer centers in the world. Through the efforts of strategic partners Sage Bionetworks and cBioPortal, the registry aggregates, harmonizes, and links clinical-grade, next-generation cancer genomic sequencing data with clinical outcomes obtained during routine medical practice from cancer patients treated at these institutions.
Job Summary:
AACR Project GENIE® is seeking an experienced Senior Biostatistician to provide statistical leadership across an international real-world clinico-genomic data consortium. This individual will serve as the primary statistical resource for the project, partnering with clinicians, scientists, data managers, and external collaborators to design, execute, and interpret observational research studies using real-world oncology data.
The successful candidate will independently develop statistical analysis plans, contribute to study protocols and publications, design appropriate analytical methodologies, and perform statistical programming in R. This role requires expertise in real-world data, including electronic health records, cancer registries, genomic sequencing data, and longitudinal clinical outcomes, as well as the ability to translate scientific questions into rigorous and reproducible statistical analyses.
This role is ideal for a senior biostatistician who enjoys working independently and leading the statistical design, programming, and interpretation of multiple concurrent studies within a collaborative multidisciplinary environment. The successful candidate will be a self-starter who takes initiative and balances big picture strategy with execution against project goals, bringing an entrepreneurial, visionary approach and the ability to conceive of, execute, and communicate innovative solutions. Additionally, the successful candidate should bring a strong passion for mission-driven causes and a commitment to advancing cancer research through high-quality, collaborative, statistical science.
Responsibilities
  • Serve as the statistical subject matter expert for AACR Project GENIE, providing consultation to investigators, collaborators, and project leadership on study design and analytical strategy.
  • Collaborate with investigators, pharmaceutical clients, and academic institutions to design observational studies using real-world clinico-genomic data
  • Develop statistical analysis plans (SAPs), define study populations, cohorts, endpoints, and analytical methods
  • Contribute statistical expertise to research protocols, study design, and publication planning
  • Perform statistical programming and analyses using R
  • Interpret results and contribute to manuscripts, abstracts, presentations and consortium reports
  • Willing to experiment with new analytic methods as needed.
  • Advise project leadership on appropriate statistical methodologies, and study design
  • Ensure analyses are reproducible, well documented, and adhere to best practices
  • Collaborate with data managers, investigators, and pharmaceutical clients to assess data quality, completeness and fitness for analysis
  • Independently lead the statistical aspects of multiple concurrent observational research studies from study conception through analysis and publication
  • Other duties as assigned

Qualifications
Education:
M.S. or Ph.D. in Biostatistics, Epidemiology, Statistics, or a closely related quantitative discipline.
Experience:
  • 5+ years of post-graduate experience providing end-to-end statistical support for observational research studies using real-world data (RWD), including electronic health records (EHRs), cancer registries, genomic data, claims data, or other longitudinal clinical data sources.
  • Demonstrated experience designing statistical analysis plans (SAPs), contributing statistical sections of research protocols, defining study cohorts, endpoints, and analytical methodologies for observational clinical research.
  • Prior peer-reviewed publications as a statistical collaborator
  • Strong proficiency in R is required, including statistical programming, data manipulation, reproducible workflows, and production-quality analytical code.
  • Experience applying statistical methods commonly used in oncology and observational research, including survival analysis, Kaplan-Meier estimation, competing risks, longitudinal analyses, regression modeling, propensity score methods, missing data approaches, and sensitivity analyses.
  • Experience collaborating with clinicians, scientific investigators, and data management teams to translate research questions into statistically rigorous study designs, with well-honed relationship building skills and outstanding, articulate, and persuasive communication, public speaking, and presentation abilities.
  • Experience interpreting and communicating statistical findings to both technical and non-technical audiences, with exceptional strategic thinking and problem-solving abilities and a proven track record of success in solving complex and dynamic situations.
  • Entrepreneurial, visionary approach with the ability to conceive of, execute, and communicate innovative solutions.
  • Must be a self-starter who takes initiative and can balance big picture strategy and execution against goals.

Preferred Qualifications:
  • Python proficiency
  • Experience working with clinico-genomic oncology datasets
  • Familiarity with REDCap or other EDC platforms
  • Experience with Git/GitHub strongly preferred

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