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Health Science Writer Jobs in Florida (NOW HIRING)

Global Virus Network

Freelance Medical/Grant Writer

Tampa, FL · On-site

$20 - $25.75/hr

The ideal candidate will have strong scientific writing skills, experience with grant development, and the ability to translate complex scientific and public health information into clear, accurate ...

Global Virus Network

Freelance Medical/Grant Writer

Tampa, FL · On-site

$20 - $25.75/hr

The ideal candidate will have strong scientific writing skills, experience with grant development, and the ability to translate complex scientific and public health information into clear, accurate ...

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How much do health science writer jobs pay per hour?

As of Jul 18, 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 are popular job titles related to Health Science Writer jobs in Florida? For Health Science Writer jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Health Science Writer jobs in Florida look for? The top searched job categories for 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:
Health Science Writer jobs near you

Health Science Specialist

North Florida Foundation for Research and Education Inc

Gainesville, FL • On-site

$57K - $69K/yr

Full-time

Re-posted yesterday

Job description

Supports the enrollment of patients into clinical trials through recruitment, screening, enrollment and follow up of eligible subjects according to protocol requirements.

• Collaborates with the principal investigator to meet or exceed study enrollment.

• Reviews the study design and inclusion/exclusion criteria with physician and patient.

• Ensures the protection of study patients by verifying informed consent procedures and adheres to protocol requirements/compliance and provides close monitoring of subjects while on study.

• Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review. Monitors data for missing or inaccurate data and respond to queries.

• Creates study specific tools for source documentation when not provided by sponsor.

• Collects, completes, and enters data into study specific case report forms or electronic data capture systems.

• Generates and tracks drug shipments, device shipments and supplies as needed.

• Assists with sample collection to include environmental sample collection, packing and shipping of samples.

• Assists with study relevant forms required for various regulatory and oversight committees.

• Reports and follows up on serious adverse events as necessary.

• Implements study-specific communications.

• Maintains accurate and complete records including regulatory documents when applicable, signed informed consent forms, source documentation, drug dispensing logs, device utilization logs, subject logs and study-related communications.

• Tracks and reports adverse events, serious adverse events, protocol waivers, deviations, and violations.

• Attends study specific on site meetings, Investigator meetings, conference calls and monthly CRC meetings as required or asked to do so.

• Apprises principal investigator of all study specific medical issues for guidance.

• Assists Sponsor, VA, FDA, IRB and other audit teams as needed.

• Reviews and responds to any monitoring and auditing findings

• Maintains patient confidentiality according to ethical and legal requirements.

• Assists in providing coverage for other projects and investigators as necessary or when asked to do so.

• Practice and adhere to the "VA Rules of Behavior."

• Performs other related duties as assigned by management.


SUPERVISORY RESPONSIBILITIES:

• This job has no supervisory responsibilities.

QUALIFICATIONS:

• Bachelor's Degree (BA) from four-year college or university, or four years of related experience and/or training, or equivalent combination of education and experience.

• Certificates, licenses and registrations preferred but not required:

o Specialty research certification such as ACRP’s CCRA, CCRC, ACRP-CP or SOCRA’s CCRP.

• Computer skills required: Microsoft Office Suite

• Other skills required:

o Working knowledge of medical and research terminology.

o Working knowledge of federal regulations for human subject protections and Good Clinical Practices (GCP).

o Ability to communicate and work effectively with a diverse team of professionals.

o Excellent organizational and prioritizing capabilities.

o Strong computer skills with demonstrated abilities using clinical trial database, electronic data capture.

o Excellent interpersonal skills, detailed oriented and meticulous.

o Excellent professional writing and communication skills.

o Ability to demonstrate proficient achievement of ‘Intermediate CRC’ based on ACRP Core.

o Specimen and/or tissue collection, handling & processing.

o Phlebotomy experience


Monday - Friday 7am - 4pm
on-site
40 hours per week