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How much do commission health science writer jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for commission health science writer in the United States is $38.94, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $47.12 per hour, depending on experience, location, and employer.

What is a Commission Health Science Writer?

A Commission Health Science Writer is a professional who creates health-related scientific content on a contract or project basis, rather than as a full-time employee. They are typically hired by organizations such as healthcare companies, scientific journals, or public health agencies to write articles, reports, educational materials, or marketing content. These writers use their expertise in science and medicine to communicate complex information clearly and accurately to various audiences. Commission Health Science Writers often work remotely and may manage multiple projects for different clients simultaneously.

How does a Commission Health Science Writer typically manage competing deadlines and multiple assignments from different clients?

As a Commission Health Science Writer, juggling multiple projects for various clients is a regular part of the workflow. Effective time management, clear communication, and organizational tools are crucial to prioritize assignments and meet deadlines. Writers often use editorial calendars and project management software to track progress, and check in with clients regularly to clarify expectations or negotiate timelines if needed. Flexibility and the ability to quickly adapt to new topics or changing requirements also help ensure high-quality, timely deliverables.

What are the key skills and qualifications needed to thrive as a Commission Health Science Writer, and why are they important?

To thrive as a Commission Health Science Writer, you need a solid background in life sciences or healthcare, strong research skills, and excellent written communication, often supported by a relevant degree. Familiarity with scientific databases, citation tools like EndNote, and content management systems is typically required. Exceptional attention to detail, the ability to translate complex data into accessible language, and strong organizational skills help writers stand out. These capabilities ensure the production of accurate, engaging, and credible health-related content that meets editorial and scientific standards.
What cities are hiring for Commission Health Science Writer jobs? Cities with the most Commission Health Science Writer job openings:
What are the most commonly searched types of Health Science Writer jobs? The most popular types of Health Science Writer jobs are:
What states have the most Commission Health Science Writer jobs? States with the most job openings for Commission Health Science Writer jobs include:
Commission 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

Posted 24 days ago

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