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Senior Science Writer Jobs in Spring City, PA (NOW HIRING)

Legend Biotech US

Sr. Scientist, Toxicology

Philadelphia, PA · Hybrid

$92K - $126K/yr

Legend Biotech is seeking a Sr. Scientist, Toxicology as part of the Early Drug Development team ... Scientific writing, communication, and presentation skills. * Ability to work independently while ...

Frontage Laboratories

Senior Scientist

Exton, PA · On-site

$88K - $120K/yr

Senior Scientist-Biologics(ADA/NAB) Title: Senior Scientist, Biologics Location : Exton,PA ... Excellent oral and written communication skills. * Good knowledge and application of GLP with the ...

Legend Biotech US

Sr. Scientist, Toxicology

Philadelphia, PA · On-site

$92K - $126K/yr

Legend Biotech is seeking a Sr. Scientist, Toxicology as part of the Early Drug Development team ... Scientific writing, communication, and presentation skills. * Ability to work independently while ...

Frontage Laboratories

Scientist Senior

Exton, PA · On-site

$88K - $120K/yr

Sr. Scientist - CMC Analytical Services Title : Sr. Scientist Location: Exton, PA Full-time ... Good verbal and written communication skills. * Good analytical, logical thinking and problem ...

Legend Biotech US

Senior Scientist

Philadelphia, PA · Hybrid

$92K - $126K/yr

Legend Biotech is seeking a Senior Scientist as part of the R&D Leadership Development Program ... Excellent verbal and written communication skills, with the ability to effectively present complex ...

Legend Biotech US

Scientist

Philadelphia, PA · On-site

Legend Biotech is seeking a Senior Scientist as part of the R&D Leadership Development Program ... Excellent verbal and written communication skills, with the ability to effectively present complex ...

Synchrony Group

Senior Medical Writer

West Chester, PA · On-site

Synchrony consists of integrated groups of medical-scientific, clinical, creative, commercial, and ... The Senior Medical Writer: 1) writes original content for publications activities, and other ...

Synchrony Group

Senior Medical Writer

West Chester, PA · On-site +1

Synchrony consists of integrated groups of medical-scientific, clinical, creative, commercial, and ... The Senior Medical Writer: 1) writes original content for publications activities, and other ...

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Showing results 1-20

All JobsScience Writer JobsSenior Science Writer JobsSenior Science Writer Jobs in Spring City, PA

Senior Science Writer information

See Spring City, PA salary details

$30.3K

$91.9K

$169.7K

How much do senior science writer jobs pay per year?

As of Jul 30, 2026, the average yearly pay for senior science writer in Spring City, PA is $91,866.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,500.00 and $100,200.00 per year, depending on experience, location, and employer.

What are typical daily responsibilities for a Senior Science Writer?

A Senior Science Writer typically drafts and edits articles, research summaries, press releases, and technical documents for print or digital publication. They often interview scientists, attend research meetings, and translate complex data into accessible language for various audiences. Collaboration with editors, graphic designers, and subject matter experts is common to ensure accuracy and engaging presentation. Additionally, Senior Science Writers may mentor junior writers, contribute to editorial strategy, and help coordinate publication schedules, offering a dynamic and multifaceted work environment.

What are the key skills and qualifications needed to thrive in the Senior Science Writer position, and why are they important?

To thrive as a Senior Science Writer, you need exceptional writing and editing skills, advanced scientific literacy (often supported by a degree in a science discipline), and a proven track record in science communication. Familiarity with publishing platforms, reference management tools, and proficiency in editing or style guide systems (such as AMA or APA) is commonly expected. Outstanding soft skills include attention to detail, the ability to translate complex concepts for diverse audiences, project management, and collaborative teamwork. These capabilities ensure scientifically accurate, engaging content that meets both editorial standards and audience needs, while supporting collaboration with subject matter experts.

What is a Senior Science Writer job?

A Senior Science Writer is a professional who creates and edits scientific content for various audiences, including researchers, policymakers, and the general public. They work closely with scientists, subject matter experts, and communication teams to translate complex scientific information into clear, engaging, and accurate materials. Their work may include writing articles, reports, press releases, white papers, and grant proposals. They often have a background in science or journalism and must possess strong writing, research, and editing skills. Depending on the organization, they may also oversee junior writers, manage projects, and ensure consistency in scientific messaging.

Senior Science Writer jobs near you
Infographic showing various Senior Science Writer job openings in Spring City, PA as of July 2026, with employment types broken down into 87% Full Time, 4% Temporary, and 9% Contract. Highlights an 74% In-person, 5% Hybrid, and 21% Remote job distribution, with an average salary of $91,866 per year, or $44.2 per hour.

Sr. Scientist, Toxicology

Legend Biotech US

Philadelphia, PA • Hybrid

$92K - $126K/yr

Other

Re-posted 13 days ago

Job description

Legend Biotech is seeking a Sr. Scientist, Toxicology as part of the Early Drug Development team based in Somerset, NJ or Philadelphia, PA.

Role Overview

Legend Biotech is seeking a Sr. Scientist, Toxicology to support nonclinical development and safety assessment across cell and gene therapy programs. This individual will contribute to nonclinical strategy from discovery through IND-enabling development and support regulatory submissions for innovative advanced therapies. The role requires scientific expertise in toxicology, a foundation in pharmacology, understanding of regulatory expectations, and the ability to work effectively across cross-functional teams in a fast-paced biotech environment.

Key Responsibilities

  • Support toxicology activities for discovery and development-stage cell and gene therapy programs.
  • Design, monitor, interpret, and report nonclinical safety, pharmacology, biodistribution, and pharmacokinetic studies.
  • Support integrated interpretation of toxicology and pharmacology data to enable candidate selection, risk assessment, and program progression.
  • Contribute to study strategy and execution at CROs, including protocol review, study monitoring, data interpretation, and final report review.
  • Partner closely with Pharmacology, CMC, Clinical, Regulatory Affairs, and Program Management teams to advance development programs.
  • Support preparation of regulatory documents, including briefing packages, pre-IND/IND submissions, investigator brochures, and responses to health authority questions.
  • Contribute to safety risk assessments related to target biology, exaggerated pharmacology, off-target effects, immunogenicity, genome-related risks, and long-term safety.
  • Interpret complex nonclinical datasets and communicate key findings and recommendations clearly to internal stakeholders.
  • Stay current with scientific and regulatory advances relevant to toxicology, pharmacology, and cell and gene therapy development.
  • Support in vivo pharmacology activities, when needed, through integrated assessment of efficacy, disposition, and safety findings.

Requirements

  • Ph.D., DVM, PharmD, or equivalent degree in Toxicology, Pharmacology, Immunology, or a related discipline.
  • Minimum of 5 years of experience in nonclinical toxicology or a related field within biotechnology or pharmaceutical R&D, with working knowledge of pharmacology principles.
  • Experience supporting cell therapy, gene therapy, biologics, or other advanced therapeutic platforms preferred.
  • Working knowledge of GLP toxicology studies, nonclinical pharmacology studies, CRO management, and regulatory expectations for nonclinical development.
  • Experience contributing to IND/CTA-enabling packages and global regulatory submissions is highly desirable.
  • Understanding of FDA, EMA, and ICH regulations pertaining to toxicology and cell and gene therapy development.
  • Scientific writing, communication, and presentation skills.
  • Ability to work independently while thriving in a collaborative, matrixed team environment.

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