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Mid Level Teen Medical Writer Jobs (NOW HIRING)

Medical Writer

Princeton, NJ · On-site

$80K - $130K/yr

... level qualifications, experience, and skills ... While most offers typically fall within the low to mid-point of the range, we may extend an offer ...

Medical Writer

Princeton, NJ · On-site

$80K - $130K/yr

... level qualifications, experience, and skills ... While most offers typically fall within the low to mid-point of the range, we may extend an offer ...

University-level medical or technical writing course(s) or equivalent experience in science/technical writing. Evidence of medical writing career development desirable, eg, American Medical Writers ...

A Medical Writer acts as a content expert, a face, and a voice for AdMed, Inc. The role involves ... Attend client meetings, listening to their needs, offering your feedback, and building a level of ...

Senior Medical Writer

The Lakes, NV · Remote

$142K - $195K/yr

... Experience Level: Mid-Senior ───── Job Overview ───── We are seeking an ... Medical Writer to support clinical development and regulatory documentation activities within a ...

About the Role We're looking for an experienced regulatory medical writer to act as our in-house ... The base salary range for this role is competitive, depending on experience and level (Tier 1, San ...

Medical Writer - Publications Nucleus Global is an international medical communications agency ... local level and across a broad spectrum of therapy areas. Our success has led to continued ...

Medical Writer Location: Paramus, NJ, 07652 Job Type: Temporary Assignment Duration: 5 Months Work ... High level of Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) * Experience with ...

Medical Writer - Publications Nucleus Global is an international medical communications agency ... local level and across a broad spectrum of therapy areas. Our success has led to continued ...

Medical Writer

Manhattan, NY · Remote

$65K - $85K/yr

And we're looking for people who fit that profile to help take our business to the next level ... Writing/Content Development * Research, learn, and simplify complex scientific/medical information ...

Senior Medical Writer

New York, NY · Hybrid

$90K - $100K/yr

Senior Medical Writers take a leading role across projects, providing strategic advice to clients ... A degree level or higher qualification in a scientific discipline (minimum GPA 3.3). We welcome ...

Strong written and verbal communication skills with the ability to collaborate across teams Preferred Certifications include: * AWS Certified Cloud Practitioner * Microsoft Certified: Azure ...

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Mid Level Teen Medical Writer information

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How much do mid level teen medical writer jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for mid level teen medical 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.
What cities are hiring for Mid Level Teen Medical Writer jobs? Cities with the most Mid Level Teen Medical Writer job openings:
What are the most commonly searched types of Teen Medical Writer jobs? The most popular types of Teen Medical Writer jobs are:
What states have the most Mid Level Teen Medical Writer jobs? States with the most job openings for Mid Level Teen Medical Writer jobs include:
Infographic showing various Mid Level Teen Medical Writer job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, and 5% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.

Medical Writer

Systimmune

Princeton, NJ • On-site

$80K - $130K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 18 days ago


Job description

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
 

The medical writer will be responsible for the management and oversight of assigned medical writing projects, including clinical study protocols and reports, investigational new drug applications (INDs), investigator brochures, reviewing informed consent forms and regulatory briefing materials. They will be accountable for ensuring that all documents are written according to established templates and guidance, and that they are of the highest quality with respect to scientific content, organization, accuracy, regulatory guidelines, clarity of presentation, and structure.  
This is an onsite position that is located at our Princeton, NJ office.
 

Key Responsibilities

  • Write, edit and/or manage the production of high-quality clinical documentation including clinical study protocols, synopses, and clinical study reports for submission to regulatory authorities in support of marketing applications and BLAs.  

  • Act as a member of clinical trial teams  

  • Follow and track clinical documentation milestones  

  • Write/edit other strategic documents, as required  


Qualifications

  • Master's degree in a life sciences discipline or at least 3 to 4 years of experience as a medical writer in the pharmaceutical industry PhD with at least 1 year experience as a medical writer in the pharmaceutical industry 

  • Excellent writing and effective communication skills  

  • Proven interpersonal, organizational and problem-solving skills in a matrix management environment.  

  • Knowledge of FDA and ICH guidelines  

  • Skilled in clinical data interpretation  

  • Proven experience writing/supporting major documents (eg,. protocols, CSRs, ISE, ISS, and Clinical Overview etc.)  

Preferred Qualifications

  • Knowledge of drug development and regulatory requirements to guide document organization  

  • Project management experience including the use of negotiation and influence to ensure document timelines are met while maintaining high quality
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Compensation and Benefits:
The expected base salary range for this position is $80,000 - $130,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s level qualifications, experience, and skills.
While most offers typically fall within the low to mid-point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceeds the requirements of the role.
 
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
 
We offer an opportunity for you to learn and grow while making significant contributions to the company’s success.
 
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.

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