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Health Science Writer Jobs in Florida (NOW HIRING)

Scientific Writing 30%: Utilize training, knowledge and expertise in the field to summarize external scientific research and public health findings for researchers at UAB. Summarize UAB immunology ...

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Health Science Writer information

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$10

$28

$43

How much do health science writer jobs pay per hour?

As of Jul 19, 2026, the average hourly pay for health science writer in Florida is $28.87, according to ZipRecruiter salary data. Most workers in this role earn between $19.57 and $36.44 per hour, depending on experience, location, and employer.

How much do science writers get paid?

Science writers, including health science writers, typically earn between $50,000 and $90,000 annually, depending on experience, education, and the employer. Freelance writers may charge per word or project, with rates ranging from a few cents to several dollars per word. Advanced skills in medical terminology and familiarity with scientific tools can influence earning potential.

What is a Health Science Writer job?

A Health Science Writer researches, writes, and edits content related to medical and scientific topics for various audiences. They may create articles, reports, white papers, or marketing materials for healthcare organizations, medical journals, or pharmaceutical companies. Their role involves translating complex scientific information into clear, accurate, and engaging content that is accessible to professionals or the general public. Strong research skills, an understanding of medical terminology, and the ability to communicate technical concepts effectively are essential for this role.

How to become a health writer?

To become a health science writer, develop strong writing skills and a background in health, science, or related fields through a degree or coursework. Gaining experience with research, medical terminology, and writing for scientific or lay audiences, along with familiarity with editing tools and industry standards, can improve job prospects.

What does a health science writer do?

A health science writer creates clear, accurate content about medical, scientific, and health topics for audiences such as healthcare professionals, patients, or the general public. They research, analyze, and translate complex scientific information into accessible articles, reports, or educational materials, often using tools like style guides and referencing scientific literature. Strong writing skills, knowledge of medical terminology, and attention to detail are essential for this role.

What are typical daily responsibilities for a Health Science Writer?

As a Health Science Writer, you’ll spend your days researching scientific literature, distilling complex health information into clear and accessible content, and collaborating with subject matter experts such as medical professionals or researchers. You may write articles, reports, web content, or patient education materials, ensuring accuracy and adherence to client or publication guidelines. Regular tasks also include fact-checking, editing drafts based on feedback, and meeting tight deadlines. Working in this role often means balancing multiple projects while staying up-to-date with the latest developments in health science.

How much do freelance health writers make?

Freelance health writers typically earn between $30 and $100 per hour, depending on experience, expertise, and the complexity of the topics. Many also charge per project, with rates ranging from a few hundred to several thousand dollars for comprehensive articles or reports. Earnings can vary widely based on skill level, niche specialization, and client demand.

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

To thrive as a Health Science Writer, you need a strong grasp of scientific concepts, excellent research abilities, and superb written communication skills, often supported by a degree in health sciences, journalism, or a related field. Familiarity with reference management tools, medical databases, and style guides such as AMA or APA is commonly expected. Outstanding soft skills include attention to detail, critical thinking, and the ability to translate complex information for various audiences. These skills ensure accurate, engaging, and trustworthy health content that meets the needs of both experts and the general public.

What are the most commonly searched types of Health Science Writer jobs in Florida? The most popular types of Health Science Writer jobs in Florida are:
What cities in Florida are hiring for Health Science Writer jobs? Cities in Florida with the most Health Science Writer job openings:
Medical Writer II/ Sr Medical Writer

Other

Medical, Dental, Vision, Retirement, PTO

Posted 13 days ago


Syneos Health rating

8.1

Company rating: 8.1 out of 10

Based on 22 frontline employees who took The Breakroom Quiz

33rd of 74 rated pharmaceutical


Job description

Medical Writer II/ Sr Medical Writer

Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.
Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver - for one another, our customers, and, most importantly, for those in need.
Discover what your 25,000 future colleagues already know:
Why Syneos Health
* We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
* We are committed to building an inclusive culture - where you can authentically be yourself. Central to this is our purpose - Driven to Deliver - which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone's life.
* We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.

Job Responsibilities

Job Summary
Senior medical writer on clinical study or regulatory project teams. Writes, edits, and coordinates content for clinical/regulatory documents while serving as the primary technical contact with the internal team and the client.

Core Responsibilities
Leads the clear and accurate completion of medical writing deliverables, ensuring scientific information is presented clearly and accurately. Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision. Leads the resolution of comments from the client.
Completes a variety of documents that may include clinical study protocols and clinical study protocol amendments; clinical study reports; patient narratives; annual reports; investigator brochures; informed consents; annual reports; plain language summaries; periodic safety update reports, clinical development plans; IND submissions; integrated summary reports; NDA and eCTD submissions; journal manuscripts; and abstracts, posters, and presentations for scientific meetings.
Adheres to established regulatory standards, including, but not limited to, ICH E3 guidelines, as well as company standard operating procedures, client standards, and company and/or client approved-templates, authorship requirements, and style and formatting guides, when completing medical writing projects, on time and on budget.
Coordinates quality and editorial reviews. Ensures source documentation is managed appropriately. Leads team document reviews, and reviews documents as needed.
Acts as peer reviewer for internal team to ensure document scientific content, clarity, overall consistency, and proper format.
Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency. Provides feedback to further define statistical output required and document needs.
Interacts and builds good working relations with clients, department head, and peers in data management, biostatistics, regulatory affairs, and medical affairs, as necessary, to produce writing deliverables.
Performs online clinical literature searches and complies with copyright requirements.
Identifies and proposes solutions to resolve issues, escalating as appropriate. Provides technical support, training, and consultation to department and other company staff. May contribute to development of internal materials and presentations or changes to internal process, standard practices, and capabilities.
Mentors and leads less experienced medical writers on complex projects, as necessary.
Develops deep expertise on key topics in the industry and the regulatory requirements and guidelines that affect medical writing.
Aware of budget specifications for assigned projects, working within the budgeted hours and communicating status and changes to medical writing leadership.
Completes required administrative tasks within the specified timeframes.
Performs other work-related duties as assigned.
Minimal travel may be required (less than 25%).
Qualifications


4 Year / Bachelors Degree
Bachelor's degree in a relevant discipline with relevant writing experience; graduate degree preferred.

Additional Qualifications
3-5 years of relevant experience in science, technical, or medical writing.
Experience working in the biopharmaceutical, device, or contract research organization industry required.
Strong understanding of FDA and ICH regulations, other regulatory guidelines, and/or good publication practices strongly required.


Experience writing relevant document types required.
Extensive knowledge of English grammar and ability to communicate clearly; strong familiarity with AMA Manual of Style.

At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.

Salary Range:

$70,100.00 - $145,000.00

The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate's qualifications, skills, competencies, and proficiency for the role.

Get to know Syneos Health


Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

http://www.syneoshealth.com

Additional Information


Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.


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