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Flexible Health Science Writer Jobs (NOW HIRING)

Yale University

Sr. Scientific Research Writer

... health. The position is designed with flexible effort (variable FTE) and will support externally ... science domains. * Lead or support systematic, scoping, and narrative reviews. * Synthesize ...

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

As of Jun 10, 2026, the average hourly pay for flexible health science writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.

How does a Flexible Health Science Writer typically collaborate with medical experts and editors during content development?

As a Flexible Health Science Writer, you will frequently interact with subject matter experts, such as physicians or researchers, to ensure the accuracy and credibility of your content. Collaboration often takes place through virtual meetings, interviews, and email correspondence, especially given the remote or flexible nature of the position. You'll also work closely with editors who review your drafts for clarity, adherence to style guidelines, and regulatory compliance. Regular feedback helps refine your writing and ensures the final content meets both scientific standards and audience needs.

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

To thrive as a Flexible Health Science Writer, you need a strong background in health sciences or a related field, excellent research abilities, and proven writing skills, often supported by a relevant degree or experience. Familiarity with reference management tools, content management systems, and adherence to scientific writing standards like AMA or APA style is crucial. Outstanding attention to detail, adaptability, and the ability to communicate complex information clearly are vital soft skills. These skills ensure accurate, credible, and accessible health content tailored for diverse audiences and publication formats.

What are Flexible Health Science Writers?

Flexible Health Science Writers are professionals who create clear, accurate, and engaging health-related content for various audiences, such as patients, healthcare providers, or the general public. The 'flexible' part refers to their ability to work remotely, on contract, or on a freelance basis, which allows for adaptable work schedules and environments. They may write articles, reports, educational materials, or marketing content, often translating complex scientific information into language that is easy to understand. These writers may work for healthcare organizations, publishers, medical communications agencies, or as independent consultants.

What is the difference between Flexible Health Science Writer vs Medical Writer?

AspectFlexible Health Science WriterMedical Writer
CredentialsOften requires a degree in health sciences, life sciences, or related fields; certifications are a plusTypically requires a degree in health sciences, life sciences, or related fields; certifications like AMWA or EMWA are common
Work EnvironmentFreelance, remote, or contract-based; varies by projectFull-time or freelance; often remote or office-based
Employer & IndustryHealth and science media, pharmaceutical companies, research organizationsPharmaceutical, biotech, medical communication agencies, healthcare publishers

Flexible Health Science Writers focus on adaptable, project-based work often in media or communications, while Medical Writers typically produce regulatory or clinical documentation within healthcare industries. Both roles require health sciences background and offer remote opportunities, but their primary outputs and client types differ.

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Flexible 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