Top 80 Home based medical writer Jobs in Remote

Medical Writer
Celerion —Remote
- Full-time
- Remote
- Bachelor of Science
- Clinic experience
- Mid-level
Quick Apply
Medical Writer / Clinical Document Author
PVR Cinemas —Remote
- $50 - $80 an hour
- Contract
- Remote
- Medicine
- 5 years
- No experience needed
- Flexible schedule
Quick Apply
6h
Medical Writer
BGBx —Remote
- $70,000 - $95,000 a year
- Full-time
- Remote
- Medicine
- Research
- Mid-level
- Paid holidays
- Health insurance
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Medical Writer
Biodesix, Inc. —Remote
- $90,000 - $130,000 a year
- Full-time
- Remote
- Mid-level
- 3 years
- Databases
- Paid holidays
- Disability insurance
Quick Apply
5d
Medical Writer (Remote, US)
Maquet Cardiovascular LLC —Boston, MA
- $105,000 - $115,000 a year
- Remote
- Microsoft Excel
- Microsoft Outlook
- 3 years
- Commuter assistance
- Disability insurance
Medical writer life science
Blue Novius —Remote
- Full-time
- Remote
- English
- Doctor of Philosophy
- Organizational skills
Medical Writer / Clinical Document Author
AuraOne Human Data —Remote
- Remote
- Bilingual
- Writing skills
- Mid-level
12d
Senior Medical Writer - FSP
Parexel —Remote
- Remote
- English
- Bachelor's degree
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Associate Medical Writer Talent Community
Envision Pharma Group —Remote
- Full-time
- Remote
- Medicine
- Doctor of Philosophy
- Entry level
Health Writer & Content Creator
Thrive Global Holdings, Inc. —Remote
- $115,000 - $130,000 a year
- Full-time
- Remote
- Mid-level
- 10 years
- Health insurance
- Dental insurance
Quick Apply
Senior Medical Writer
BGBx —Remote
- $90,000 - $115,000 a year
- Remote
- Research
- Travel
- 1 year
- Paid holidays
- Health insurance
Quick Apply
Senior Medical Writer
Regeneron —Remote
- $128,600 - $210,000 a year
- Remote
- Microsoft Word
- Mid-level
- 3 years
- Health insurance
- Dental insurance
Medical Writer
Knowesis, Inc. —East Orange, NJ
- $85,000 - $89,000 a year
- Full-time
- Remote
- 5 years
- Mid-level
- Presentation skills
- Disability insurance
- Health insurance
Medical Writer (Publications)
Red Nucleus —Remote
- Full-time
- Remote
- Medicine
- Mid-level
- Doctor of Philosophy
- Paid time off
- Employee assistance program
Regulatory Writer and/or Regulatory QC/ Editor (Temporary)
Vir Biotechnology —Remote
- $90 - $120 an hour
- Temporary
- Remote
- 5 years
- Mid-level
- Analysis skills
Quick Apply
Medical Writer
BOLDSCIENCE —Remote
- Remote
- Medicine
- Mid-level
- Doctor of Philosophy
Sr. Medical Writer
Vue Health —Remote
- Up to $115,000 a year
- Full-time
- Remote
- Medicine
- Microsoft Outlook
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Sr. Medical Writer Peripheral Vascular Med Device (U.S. Remote)
MicroVention, Inc. —Aliso Viejo, CA
- $145,000 - $155,000 a year
- Remote
- Microsoft Excel
- 5 years
- Bachelor of Science
Medical Patient Language Writing Specialist
Cohere Health —Remote
- $85,000 - $92,000 a year
- Remote
- Nursing
- 5 years
- Bachelor's degree
- Paid parental leave
- Health savings account
Quick Apply
Senior Medical Writer
BluPrint Oncology Concepts, LLC —Remote
- $80,000 - $105,000 a year
- Full-time
- Remote
- Nursing
- Medicine
- Microsoft Outlook
Quick Apply
12d

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home based medical writer jobs near remote

Medical Writer

Celerion -
Remote

Quick Apply

Job Details

Full-time

Qualifications

Technical editing
Technical writing for researchers
Medical writing
Content writing

Full Job Description

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.

We are searching for a full-time Medical Writer to work remotely. This position will analyze and interpret safety results of clinical trials. Compile, write and edit clinical study reports and other industry documents. Confirm accurate classification of events and medications using standardized coding systems.

Responsibilities

Analyze and interpret all types of medical results including, but not limited to the following: vital signs, clinical laboratory values, adverse events, electrocardiograms (ECGs), diagnostic procedures, and various pharmacodynamic (PD) endpoints.Compile and write Phase I and Phase II clinical trial documents including, but not limited to the following: clinical study reports (CSRs), stand-alone safety narratives, and synoptic CSRs.
Review/evaluate study results to determine whether or not the safety objectives and/or endpoints were met, accurately reflecting the results in the safety text.
Perform peer QC function of safety text prior to inclusion in the CSR.Review reports for completeness and accuracy assuring that the safety text fits into the CSR as whole and recommending changes or rewriting, as appropriate.
As the project Report Lead on a multi-disciplinary scientific team, ensoure quality and on-time delivery of scientific reports.
Monitor content of editorial comments received prior to incorporation into the report to assure report text comments are accurate and support the objectives and/or endpoints.
Assure deliverables are compliant with applicable regulatory standards (i.e. Good Clinical Practice, International Conference on Harmonisation guidelines) and client specifications.
Use technology to work with international teams (e.g., WebEx™,Veeva, Microsoft® 365 applications, SharePoint®, and SmartSheet).
Lead-Project-related client communication
Interact with internal departments (e.g. data management, project management, business development, etc.).
Participate in functions required to ensure success of department and/or market segment team.

Requirements

Bachelor's degree and/or professional license in a medical or scientific field (RN, BS, RPh, MS, MPH) required or equivalent experience.
1-3 years experience in hospital/clinical setting or interpreting medical or clinical results.
Professional writing and editing skills for accurate and concise reporting of clinical trial results; ability to interpret and present data in preparing a coherently written document.
Detail-oriented, thorough, and methodical.
Ability to work without close supervision and ability to work under pressure.
Ability to multi-task and to respond rapidly to changing priorities and aggressive timelines.
Excellent communication/ interpersonal skills.
Knowledge of medical, pharmaceutical, and/or clinical research concepts preferred.

Celerion Values: Integrity Trust Teamwork Respect

Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.

Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as "Not Junk" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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