ZipRecruiter

Log In

1

Science Writer Jobs in Hamden, CT (NOW HIRING)

Cooper Companies

Senior Medical Writer

Trumbull, CT · On-site

The Senior Medical Writer is responsible for developing, writing, and managing high-quality ... Master's degree in Life Sciences or related field preferred. * Our Benefits : As an employee of ...

CooperCompanies

Senior Medical Writer

Trumbull, CT · On-site

The Senior Medical Writer is responsible for developing, writing, and managing high-quality ... Stay updated on scientific literature and regulatory changes within the company's therapeutic area.

The Lee Company

Marketing Content Writer

Westbrook, CT · On-site

... scientific instrument, oil tool, and automotive industries. Lee products are recognized worldwide ... Marketing Content Writers play an important role at The Lee Company, supporting the company ...

Varsity Tutors

High School Science Tutor

New Haven, CT · Remote

$40/hr

Guides students through designing experiments, analyzing quantitative data, writing laboratory reports, and applying scientific reasoning to real-world problems. Emphasizes connecting theory to ...

Varsity Tutors

High School Science Tutor

Bridgeport, CT · Remote

$40/hr

Guides students through designing experiments, analyzing quantitative data, writing laboratory reports, and applying scientific reasoning to real-world problems. Emphasizes connecting theory to ...

Collabera

Technical Writer

North Haven, CT

Technical writing, desktop publishing, and translation management for NPD project document requirements, including instructions for use (IFUs), user's guides, service manuals, and Technical ...

Whelen Engineering

Technical Writer 1

Chester, CT · On-site

Technical Writer 1 Department: Engineering (126) CT Employment Type: Full Time Location: Chester, CT Description Summary : supports new product development by working with cross-functional teams to ...

Honeywell

Senior Technical Writer

Guilford, CT

$83K - $104K/yr

As a Senior Tech Writer here at Honeywell, you will lead and manage a team of technical writers to create clear, concise, and accurate technical documentation. You will develop and implement ...

Honeywell

Senior Technical Writer

Seymour, CT

$83K - $104K/yr

As a Senior Tech Writer here at Honeywell, you will lead and manage a team of technical writers to create clear, concise, and accurate technical documentation. You will develop and implement ...

Honeywell

Senior Technical Writer

Waterbury, CT

$83K - $104K/yr

As a Senior Tech Writer here at Honeywell, you will lead and manage a team of technical writers to create clear, concise, and accurate technical documentation. You will develop and implement ...

next page

Showing results 1-20

All JobsScience Writer JobsScience Writer Jobs in Hamden, CT

Science Writer information

See Hamden, CT salary details

$10.9K

$70.1K

$79K

How much do science writer jobs pay per year?

As of Jun 16, 2026, the average yearly pay for science writer in Hamden, CT is $70,090.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,600.00 and $73,600.00 per year, depending on experience, location, and employer.

What is a science writer's job?

A science writer creates clear, accurate, and engaging content to communicate scientific concepts to a general audience. They often work for media outlets, research institutions, or publishing companies, and use skills in research, writing, and editing to translate complex information into accessible language.

How much do science writers get paid?

Science writers' salaries vary based on experience, education, and location, but typically range from $45,000 to $85,000 annually in the United States. Freelance science writers may earn per project or word, with rates often between $0.10 and $1.00 per word. Advanced skills, a strong portfolio, and familiarity with scientific tools can lead to higher compensation.

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

To thrive as a Science Writer, you need a solid background in scientific concepts, strong research abilities, and exceptional writing and editing skills, often supported by a degree in science or journalism. Familiarity with citation management tools, content management systems, and scientific databases is usually required. Attention to detail, creativity, and the ability to communicate complex ideas clearly are essential soft skills that set outstanding candidates apart. These competencies are crucial for crafting accurate, engaging, and accessible content that effectively bridges the gap between scientific experts and the general public.

Are science writers in demand?

Science writers are in steady demand as organizations seek clear communication of complex scientific information for audiences such as the general public, policymakers, and industry professionals. The growth of digital media and scientific publishing has increased opportunities for skilled writers with expertise in science and strong writing skills, often requiring familiarity with research tools and industry standards.

What are some typical challenges Science Writers face in this role?

Science Writers often encounter the challenge of translating complex scientific concepts into clear, compelling language for a broader audience without compromising accuracy. They must stay up-to-date with the latest research and frequently juggle tight deadlines while coordinating with subject matter experts and editors. Additionally, working in a fast-paced environment sometimes requires quick adaptation to new topics or publication formats. Overcoming these challenges sharpens communication skills, broadens subject expertise, and builds a portfolio of diverse, high-impact work.

What is a Science Writer job?

A Science Writer researches, writes, and edits content about scientific topics for various audiences. They translate complex scientific information into clear and engaging articles, reports, or scripts for publications, websites, and media outlets. Science Writers may work for universities, research organizations, media companies, or as freelancers. Their work helps bridge the gap between scientists and the public by making scientific discoveries and advancements accessible and understandable.

How much does a scientific writer get paid?

Scientific writers typically earn between $50,000 and $90,000 annually, depending on experience, education, and the industry they work in. Senior or specialized writers with advanced degrees or technical expertise can earn higher salaries, especially in biotech, pharmaceuticals, or research organizations.
What are the most commonly searched types of Science Writer jobs in Hamden, CT? The most popular types of Science Writer jobs in Hamden, CT are:
What are popular job titles related to Science Writer jobs in Hamden, CT? For Science Writer jobs in Hamden, CT, the most frequently searched job titles are:
What job categories do people searching Science Writer jobs in Hamden, CT look for? The top searched job categories for Science Writer jobs in Hamden, CT are:
What cities near Hamden, CT are hiring for Science Writer jobs? Cities near Hamden, CT with the most Science Writer job openings:
Science Writer jobs near you
Infographic showing various Science Writer job openings in Hamden, CT as of June 2026, with employment types broken down into 9% As Needed, 76% Full Time, and 15% Part Time. Highlights an 53% Physical, 3% Hybrid, and 44% Remote job distribution, with an average salary of $70,090 per year, or $33.7 per hour.
Senior Medical Writer

Senior Medical Writer

Cooper Companies

Trumbull, CT • On-site

Full-time

Medical, Life, Retirement, PTO

Posted 9 days ago

Job description

The Senior Medical Writer is responsible for developing, writing, and managing high-quality clinical and regulatory documents that support compliance and product lifecycle needs for global standards such as EU MDR and FDA regulations.  This includes planning, implementing, and reporting clinical data collection for Post-Market Clinical Follow-up (PMCF) and clinical trials, ensuring adherence to global regulatory standards. The role collaborates cross-functionally to maintain clinical documentation within the Quality Management System and stays current with scientific literature and regulatory requirements.

  • Knowledge, Skills, and Abilities:
    • Strong understanding of EU MDR, FDA regulations, and ISO standards for medical devices.
    • Proficiency in document management systems and Microsoft Office Suite
    • Excellent written and verbal communication skills
    • Ability to interpret clinical data and present findings clearly
    • Analytical mindset
    • Detail-oriented, organized, and results-driven

  • Experience:

    • Preferred 5-10 years of experience in medical writing for medical devices, including CERs and PMCF documentation.

  • Education:

    • Master's degree in Life Sciences or related field preferred.

  • Our Benefits:

    As an employee of CooperSurgical, you'll receive an outstanding total compensation plan. As we believe your compensation goes beyond your paycheck, we offer a great compensation package, medical coverage, 401(k), parental leave, fertility benefits, paid time off for vacation, personal, sick and holidays, and multiple other perks and benefits. Please visit us at www.coopersurgical.com to learn more about CooperSurgical and the benefits of becoming a member of our team.

    To all agencies: Please, no phone calls or emails to any employee of CooperSurgical about this opening. All resumes submitted by search firms/employment agencies to any employee at CooperSurgical via-email, the internet or in any form and/or method will be deemed the sole property of CooperSurgical, unless such search firms/employment agencies were engaged by CooperSurgical for this position and a valid agreement with CooperSurgical is in place. In the event a candidate who was submitted outside of the CooperSurgical agency engagement process is hired, no fee or payment of any kind will be paid.

    We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender, gender identity or expression, or veteran status. We are proud to be an equal opportunity workplace.

Essential Functions & Accountabilities:

  • Author and edit clinical documents, including Clinical Evaluation Reports (CERs), literature reviews, and regulatory submissions.
  • Plan and report clinical data collection for PMCF and clinical trials nationally and internationally.
  • Ensure clinical documentation compliance with EU MDR, FDA, and other international regulatory requirements.
  • Collaborate with Global Regulatory & Clinical Affairs teams to maintain clinical documentation within the Quality Management System.
  • Stay updated on scientific literature and regulatory changes within the company's therapeutic area.
  • Participate in cross-functional projects and contribute to clinical strategy and documentation planning.
  • Support Medical Affairs for literature reviews and writing of documentation

Apply