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Scientific Medical Writer Jobs (NOW HIRING)

This role will provide medical writing support by organizing, analyzing, and interpreting scientific and statistical data. Such documents include all types of regulatory documents, including eCTD ...

Serves as lead Medical Writer for key programs. Coordinates medical writing support for programs ... Must have strong scientific and operational background. At least 3 years of experience managing ...

Medical Writer

$90K - $105K/yr

The Medical Writer is responsible for creating communications materials including but not limited ... Collaborates with other members of the Medical & Scientific Communications team to identify ...

Medical Writing Specialist Division: Strategic Medical Affairs Reports To: Medical Safety Project ... Performs scientific writing (e.g. abstracts, manuscripts, presentations). Organizes and ...

Our mission is to deliver high-quality service and technology solutions - rooted in strong science ... Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the ...

Medical Writer

Cranbury, NJ · On-site

$85K - $100K/yr

At MJH Life Sciences our success is measured by your success! If you set your standards high and ... The Medical Writer plays a critical role in creating accurate, engaging, and compliant scientific ...

Medical Writer

$78K - $102K/yr

Advance your medical writing career with purpose and impact. Work shouldn't just be something we do ... Contribute to the scientific content for new business opportunities/proposals, and when appropriate ...

Includes researching scientific literature and internal research documents and data feeding the ... Medical writing and editing capabilities. Project management experience preferred. Computer skills ...

Medical Writer Location: Paramus, NJ, 07652 Job Type: Temporary Assignment Duration: 5 Months Work ... Interpret complex scientific and clinical data and communicate findings clearly and concisely

Company Stock Grant Upon Hire A DAY IN THE LIFE OF a R&D Medical Writer As a Medical Writer, you ... A Master degree in life sciences or related scientific field. * Demonstrable experience ...

We deliver an innovative, science-based portfolio of premium flagship brands and services that span ... Job Summary The Medical Writer, Medical Information is responsible for developing accurate ...

Our mission is to deliver high-quality service and technology solutions - rooted in strong science ... Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the ...

We deliver an innovative, science-based portfolio of premium flagship brands and services that span ... Job Summary The Medical Writer, Medical Information is responsible for developing accurate ...

Acts as Lead Medical Writer on any type of writing project and can advise others on any type of ... D. in life sciences related discipline or related field * Typically requires at least 8 years of ...

Responsibilities / Position overview We're looking for a brilliant individual to join our team as a Medical Writer who demonstrates an excellent scientific understanding, an ability to tell a ...

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Scientific Medical Writer information

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$46

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How much do scientific medical writer jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for scientific medical writer in the United States is $46.27, according to ZipRecruiter salary data. Most workers in this role earn between $33.65 and $56.01 per hour, depending on experience, location, and employer.

What are the typical work settings and team dynamics for a Scientific Medical Writer?

Scientific Medical Writers commonly work in pharmaceutical companies, medical communications agencies, academic institutions, or as independent consultants, often collaborating within cross-functional teams that include researchers, clinicians, regulatory experts, and marketing professionals. Daily responsibilities involve drafting, reviewing, and revising scientific manuscripts, clinical study reports, and regulatory documents, often under tight deadlines. While some positions are office-based, there are increasing opportunities for remote or hybrid work environments. Collaboration, adaptability, and regular communication with subject matter experts are central to success in this field, as writers must ensure both scientific accuracy and audience-appropriate messaging.

What is a Scientific Medical Writer job?

A Scientific Medical Writer creates clear, accurate, and well-structured documents related to medical and scientific information. They translate complex research data into formats such as journal articles, regulatory documents, clinical study reports, and educational materials. These professionals work closely with researchers, healthcare professionals, and regulatory teams to ensure scientific accuracy and compliance with industry guidelines. Strong writing skills, scientific knowledge, and attention to detail are essential for success in this role.

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

To thrive as a Scientific Medical Writer, you need advanced scientific knowledge, exceptional writing and editing abilities, and typically a degree in life sciences or a related field. Familiarity with reference management software, publication guidelines (such as GPP or ICMJE), and medical literature databases is highly beneficial. Attention to detail, strong project management, and clear communication skills help differentiate top performers in this role. These competencies ensure the accurate, compliant, and effective communication of complex scientific information to a variety of audiences.

More about Scientific Medical Writer jobs
What cities are hiring for Scientific Medical Writer jobs? Cities with the most Scientific Medical Writer job openings:
What states have the most Scientific Medical Writer jobs? States with the most job openings for Scientific Medical Writer jobs include:
Infographic showing various Scientific Medical Writer job openings in the United States as of June 2026, with employment types broken down into 2% As Needed, 75% Full Time, 15% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $96,235 per year, or $46.3 per hour.

Job description

See Yourself at Telix

The Medical Writer will contribute to the achievement of Telix's strategic goals by leading and driving the writing process. This role will be responsible for planning and preparing a variety of clinical and regulatory documents necessary for all phases of clinical drug development.

This role will provide medical writing support by organizing, analyzing, and interpreting scientific and statistical data. Such documents include all types of regulatory documents, including eCTD summary documents (for INDs/NDAs/BLAs), clinical study reports, clinical study protocol synopses and protocols, Investigator Brochures, patient safety narratives, and briefing books, among others.

Key Accountabilities:

  • Lead the compilation, writing, and editing of high-quality regulatory documents and reports (primarily clinically oriented) including CSRs, IBs, safety narratives, safety reports, ISS, ISE, and eCTD summary documents for IND, NDA, MAA, BLA applications and amendments.
  • Interpret data, search and analyze published literature, define problems, establish facts, draw valid scientific conclusions, propose solutions or corrective actions, and compose text accordingly.
  • Work with colleagues, physicians, clinical scientists, and statisticians in a professional and organized manner to complete projects in a timely manner.
  • Collaborate with project teams to respond to heath authority questions and requests.
  • Develop and update pertinent SOPs, processes, templates, style guides, and manuals, as needed.
  • Maintain knowledge to enable ongoing execution of function as medical writing expert. Maintain working knowledge of the Telix clinical development pipeline.

Education and Experience:

  • Bachelor with a focus in science or related field required; Advance degree preferred
  • 5+ years of experience in regulatory medical writing required
  • Strong understanding of drug development, clinical study design, regulations (CFR, FDA, EMA, and ICH guidelines), and scientific principles. Understanding medical terminology and statistical methodology is a must.
  • Experience writing clinical protocols, Investigator Brochures, clinical study reports, eCTD clinical summaries, and integrated summaries of safety and efficacy.
  • The ability to accurately and clearly present clinical data; strong verbal, written, and interpersonal communication skills; and proficiency in Microsoft Word are required.
  • Strong command of English language, grammar, style, logical progression. Ability to write in a clear, concise, and persuasive manner, as well as to review and edit on all levels, from copy editing to message strengthening to major rewriting.
  • Experience and proficiency with document templates, document toolbars and proper version control.
  • Demonstrated leadership capability. Good team player characteristics. Excellent communication and interpersonal skills. Strong project management skills. Organized and self-motivated. Strong attention to detail.

Key Capabilities:

  • Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected
  • Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges
  • Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do
  • Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results
  • Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders
  • Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges
  • Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language
  • Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals
  • Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges
  • Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills