OR · Remote
$85 - $90/hr
Medical Writer Contract Position - 6 months with potential extension Position Summary Our client is ... Interpret complex clinical and scientific data and communicate findings clearly and accurately.
Quick apply
OR · Remote
$85 - $90/hr
Medical Writer Contract Position - 6 months with potential extension Position Summary Our client is ... Interpret complex clinical and scientific data and communicate findings clearly and accurately.
$75K - $85K/yr
Develop scientific copy for various deliverables on assigned brands and products * Work independently and collaboratively with medical writers and directors to develop scientifically accurate copy
$75K - $85K/yr
Develop scientific copy for various deliverables on assigned brands and products * Work independently and collaboratively with medical writers and directors to develop scientifically accurate copy
Charleston, WV · 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 ...
Charleston, WV · 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 ...
As a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical ...
As a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical ...
Philadelphia, PA · On-site
You will report into the Scientific Director What will you do... Content Creation * Serve as the client-facing lead writer on one or more accounts * Research material for assigned projects, including ...
Philadelphia, PA · On-site
You will report into the Scientific Director What will you do... Content Creation * Serve as the client-facing lead writer on one or more accounts * Research material for assigned projects, including ...
Dublin, OH · On-site
$80 - $90/hr
Advanced degree in life sciences (PhD, PharmD, MD, or MS preferred) * 5+ years of regulatory/medical writing experience in the pharmaceutical industry across several therapeutic areas * Proven ...
Dublin, OH · On-site
$80 - $90/hr
Advanced degree in life sciences (PhD, PharmD, MD, or MS preferred) * 5+ years of regulatory/medical writing experience in the pharmaceutical industry across several therapeutic areas * Proven ...
Medical Writer / Content Specialist - Healthcare Communications (Promotional) Hybrid - Philadelphia ... Our focus is helping translate complex clinical and scientific information into clear, practical ...
Medical Writer / Content Specialist - Healthcare Communications (Promotional) Hybrid - Philadelphia ... Our focus is helping translate complex clinical and scientific information into clear, practical ...
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 ...
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 ...
Blue Bell, PA · On-site +1
As a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical ...
Blue Bell, PA · On-site +1
As a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical ...
Life Science Masters degree or PhD * A minimum of 8-10 years' experience in regulatory medical writing combined with scientific and regulatory knowledge, plus in-depth knowledge of regulatory medical ...
Life Science Masters degree or PhD * A minimum of 8-10 years' experience in regulatory medical writing combined with scientific and regulatory knowledge, plus in-depth knowledge of regulatory medical ...
Yardley, PA · On-site
As a Senior Medical Writer, you will use your scientific expertise to develop and deliver innovative medical communications projects. This is an excellent opportunity for an experienced medical ...
Yardley, PA · On-site
As a Senior Medical Writer, you will use your scientific expertise to develop and deliver innovative medical communications projects. This is an excellent opportunity for an experienced medical ...
Mansfield, MA · On-site +1
Title: Sr. Medical Writer Duration: 2 years Location: Mansfield, MA 02048(100% possibility of ... Scientific Writing e.g. abstracts, manuscripts, presentations * Requires a strategic understanding ...
Mansfield, MA · On-site +1
Title: Sr. Medical Writer Duration: 2 years Location: Mansfield, MA 02048(100% possibility of ... Scientific Writing e.g. abstracts, manuscripts, presentations * Requires a strategic understanding ...
As a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical ...
As a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical ...
Durham, NC · On-site
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 ...
Durham, NC · On-site
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 ...
Cranbury, NJ · On-site
$95K - $105K/yr
At MJH Life Sciences our success is measured by your success! If you set your standards high and ... The Principal Medical Writer is responsible for the development and quality of medical content for ...
Cranbury, NJ · On-site
$95K - $105K/yr
At MJH Life Sciences our success is measured by your success! If you set your standards high and ... The Principal Medical Writer is responsible for the development and quality of medical content for ...
The Lakes, NV · Remote
$142K - $195K/yr
This fully remote opportunity is ideal for a highly skilled clinical science writer with extensive ... Medical Writing ───── Requirements ───── Bachelor's degree or higher in a ...
Quick apply
The Lakes, NV · Remote
$142K - $195K/yr
This fully remote opportunity is ideal for a highly skilled clinical science writer with extensive ... Medical Writing ───── Requirements ───── Bachelor's degree or higher in a ...
Cranbury, NJ · On-site
$55K - $60K/yr
At MJH Life Sciences our success is measured by your success! If you set your standards high and ... As a Medical Writer with the Enterprise Content Team at MJH Life Sciences ® , you will play a ...
Cranbury, NJ · On-site
$55K - $60K/yr
At MJH Life Sciences our success is measured by your success! If you set your standards high and ... As a Medical Writer with the Enterprise Content Team at MJH Life Sciences ® , you will play a ...
Boston, MA · Hybrid
$71K - $76K/yr
You will work closely with our Scientific Director, who is based in Boston and has more than 10 ... Medical Communications - Medical Writer Medical Communications at Costello Medical encompasses both ...
Boston, MA · Hybrid
$71K - $76K/yr
You will work closely with our Scientific Director, who is based in Boston and has more than 10 ... Medical Communications - Medical Writer Medical Communications at Costello Medical encompasses both ...
San Diego, CA · On-site
Life Science Master's degree or PhD * A minimum of 8-10 years' experience in regulatory medical writing combined with scientific and regulatory knowledge, plus in-depth knowledge of regulatory ...
San Diego, CA · On-site
Life Science Master's degree or PhD * A minimum of 8-10 years' experience in regulatory medical writing combined with scientific and regulatory knowledge, plus in-depth knowledge of regulatory ...
Boston, MA · On-site
$71K - $76K/yr
You will work closely with our Scientific Director, who is based in Boston and has more than 10 ... Medical Communications - Medical Writer Medical Communications at Costello Medical encompasses both ...
Boston, MA · On-site
$71K - $76K/yr
You will work closely with our Scientific Director, who is based in Boston and has more than 10 ... Medical Communications - Medical Writer Medical Communications at Costello Medical encompasses both ...
$11.54 - $17.66
0% of jobs
$17.66 - $23.78
8% of jobs
$23.78 - $29.90
12% of jobs
$32.80 is the 25th percentile. Wages below this are outliers.
$29.90 - $36.01
11% of jobs
$36.01 - $42.13
11% of jobs
The median wage is $44.87 / hr.
$42.13 - $48.25
20% of jobs
$54.04 is the 75th percentile. Wages above this are outliers.
$48.25 - $54.37
15% of jobs
$54.37 - $60.49
13% of jobs
$60.49 - $66.61
7% of jobs
$66.61 - $72.73
2% of jobs
$72.73 - $78.85
2% of jobs
$11
$46
$78
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.
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.
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.
$85 - $90/hr
Contractor
Medical, Dental
Posted 15 days ago
Company: Biotechnology Company
Title: Medical Writer
Contract Position - 6 months with potential extension
Position Summary
Our client is seeking an experienced Medical Writer to develop high-quality clinical and regulatory documents in support of clinical development and regulatory submissions. This role will partner with Clinical Development, Regulatory Affairs, Biostatistics, Medical Affairs, Quality Assurance, and external vendors to produce clear, accurate, and compliant documents.
Key Responsibilities
Author, review, and edit clinical and regulatory documents, including protocols, protocol amendments, clinical study reports, investigator’s brochures, informed consent forms, CTD clinical modules, briefing documents, safety reports, and responses to regulatory questions.
Support clinical development activities by helping prepare clinical development plans, protocols, and related study documents.
Interpret complex clinical and scientific data and communicate findings clearly and accurately.
Ensure documents comply with ICH, GCP, FDA, EMA, and other applicable regulatory guidelines.
Collaborate with cross-functional teams to manage document timelines, review cycles, and submission-ready deliverables.
Review documents prepared by internal teams or external vendors for clarity, consistency, scientific accuracy, and regulatory compliance.
Qualifications
Advanced degree preferred, such as PhD, PharmD, MD, or MSc in Life Sciences, Medicine, Pharmacy, or a related field.
Minimum 3–5 years of medical writing experience in the pharmaceutical, biotech, or CRO industry.
Strong experience writing clinical trial and regulatory submission documents.
Knowledge of drug development, clinical research, clinical study conduct, regulatory requirements, and biostatistical concepts.
Familiarity with medical terminology and coding dictionaries such as MedDRA and WHODrug.
Strong knowledge of ICH/GCP and regulatory submission requirements.
Epilepsy or neurology experience is a plus.
Veeva experience preferred.
Proficiency with Microsoft Word, Excel, PowerPoint, Adobe Acrobat, EndNote, and document management systems.
Ideal Candidate
The ideal candidate is a detail-oriented medical writer who can manage multiple projects, work independently, collaborate effectively with cross-functional teams, and produce clear, well-structured, submission-ready clinical and regulatory documents.
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Biotechnology research and development
51 - 200 Employees
King of Prussia, PA, US
2000
