Senior Medical Writer
Yardley, PA · Remote
... through regulatory challenges. The Senior Medical Writer will ensure high-quality content is ... Remote Employment Type: OTHER
Yardley, PA · Remote
... through regulatory challenges. The Senior Medical Writer will ensure high-quality content is ... Remote Employment Type: OTHER
Yardley, PA · Remote
... through regulatory challenges. The Senior Medical Writer will ensure high-quality content is ... Remote Employment Type: OTHER
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 ...
$35 - $60/hr
THE CONTRACT MEDICAL WRITER-PUBLICATIONS ROLE We are seeking an experienced Medical Writer to ... This role is remote and on an as-needed basis as determined by Sorcero project volume and the ideal ...
$35 - $60/hr
THE CONTRACT MEDICAL WRITER-PUBLICATIONS ROLE We are seeking an experienced Medical Writer to ... This role is remote and on an as-needed basis as determined by Sorcero project volume and the ideal ...
... remote) from our Durham, NC, USA office. You willbe responsible for ... Preparinga variety of clinical regulatory documents (Clinical Study Protocols, Clinical Study ...
Quick apply
... remote) from our Durham, NC, USA office. You willbe responsible for ... Preparinga variety of clinical regulatory documents (Clinical Study Protocols, Clinical Study ...
This role works closely with Clinical Affairs, Regulatory Affairs, R&D, and Quality Engineering to ... medical writing experience in the medical device or pharmaceutical industry or 7+ years general ...
This role works closely with Clinical Affairs, Regulatory Affairs, R&D, and Quality Engineering to ... medical writing experience in the medical device or pharmaceutical industry or 7+ years general ...
Canton, MI · On-site +1
Highly proficient with styles of writing for various regulatory documents * Expert proficiency with ... Mentor medical writers and other members of the project team who are involved in the writing ...
Canton, MI · On-site +1
Highly proficient with styles of writing for various regulatory documents * Expert proficiency with ... Mentor medical writers and other members of the project team who are involved in the writing ...
Philadelphia, PA · On-site +1
As a Principal Medical Writer, you will be the trusted, clientfacing lead for one or more flagship ... This role offers remote working. You will report into the Scientific Director What will you do.
Philadelphia, PA · On-site +1
As a Principal Medical Writer, you will be the trusted, clientfacing lead for one or more flagship ... This role offers remote working. You will report into the Scientific Director What will you do.
Spring House, PA · On-site +1
Remote work options may be considered on a case-by-case basis and if approved by the Company. Purpose: Within Integrated Data Analytics & Reporting (IDAR), the Regulatory Medical Writing team is ...
Spring House, PA · On-site +1
Remote work options may be considered on a case-by-case basis and if approved by the Company. Purpose: Within Integrated Data Analytics & Reporting (IDAR), the Regulatory Medical Writing team is ...
This position will be remote and located in India. Primary Responsibilities * Implements all activities related to the preparation of defined medical and regulatory documents, serving as writing lead ...
This position will be remote and located in India. Primary Responsibilities * Implements all activities related to the preparation of defined medical and regulatory documents, serving as writing lead ...
Boston, MA · On-site +1
This position will be remote and located in India. Primary Responsibilities * Implements all activities related to the preparation of defined medical and regulatory documents, serving as writing lead ...
Boston, MA · On-site +1
This position will be remote and located in India. Primary Responsibilities * Implements all activities related to the preparation of defined medical and regulatory documents, serving as writing lead ...
Spring House, PA · On-site +1
Remote work options may be considered on a case-by-case basis and if approved by the Company. Purpose: Within Integrated Data Analytics & Reporting (IDAR), the Regulatory Medical Writing team is ...
Spring House, PA · On-site +1
Remote work options may be considered on a case-by-case basis and if approved by the Company. Purpose: Within Integrated Data Analytics & Reporting (IDAR), the Regulatory Medical Writing team is ...
The Senior Medical Writer applies advanced documentation preparation and document project ... Drafts and edits documents used in the preparation of regulatory filings (eg, briefing books, eCTD ...
The Senior Medical Writer applies advanced documentation preparation and document project ... Drafts and edits documents used in the preparation of regulatory filings (eg, briefing books, eCTD ...
Durham, NC · On-site +1
... remote team settings. * Proven ability to independently write and manage complex regulatory ... medical history), military service or any basis prohibited under federal, state or local law.
New
Durham, NC · On-site +1
... remote team settings. * Proven ability to independently write and manage complex regulatory ... medical history), military service or any basis prohibited under federal, state or local law.
New
Chicago, IL · On-site +1
Remote and hybrid working options as standard * Continuous learning and professional development ... Job code: CPT407 Career opportunities Medical writing Role Publications Locations USA (Remote ...
Chicago, IL · On-site +1
Remote and hybrid working options as standard * Continuous learning and professional development ... Job code: CPT407 Career opportunities Medical writing Role Publications Locations USA (Remote ...
The Principal Medical Writer will support 4D-150, a gene therapy in late-stage development for ... Ensure consistency, scientific accuracy, and regulatory alignment across BLA components and ...
The Principal Medical Writer will support 4D-150, a gene therapy in late-stage development for ... Ensure consistency, scientific accuracy, and regulatory alignment across BLA components and ...
OR · On-site +1
Supports documents for regulatory submissions to US and global health authorities, including ... Experience using medical writing systems and technologies including Veeva RIM * Knowledge of drug ...
OR · On-site +1
Supports documents for regulatory submissions to US and global health authorities, including ... Experience using medical writing systems and technologies including Veeva RIM * Knowledge of drug ...
Boston, MA · On-site +1
$160K - $175K/yr
Collaborating with internal stakeholders (clinical scientists, regulatory strategy,medical monitors ... Experience working in hybrid/remote environments Attributes: * Teamwork and collaboration; balances ...
Boston, MA · On-site +1
$160K - $175K/yr
Collaborating with internal stakeholders (clinical scientists, regulatory strategy,medical monitors ... Experience working in hybrid/remote environments Attributes: * Teamwork and collaboration; balances ...
San Francisco, CA · On-site +1
$160K - $175K/yr
Collaborating with internal stakeholders (clinical scientists, regulatory strategy,medical monitors ... Experience working in hybrid/remote environments Attributes: * Teamwork and collaboration; balances ...
San Francisco, CA · On-site +1
$160K - $175K/yr
Collaborating with internal stakeholders (clinical scientists, regulatory strategy,medical monitors ... Experience working in hybrid/remote environments Attributes: * Teamwork and collaboration; balances ...
Durham, NC · On-site +1
... remote team settings. * Proven ability to independently write and manage complex regulatory ... medical history), military service or any basis prohibited under federal, state or local law.
New
Durham, NC · On-site +1
... remote team settings. * Proven ability to independently write and manage complex regulatory ... medical history), military service or any basis prohibited under federal, state or local law.
New
Billerica, MA · On-site +1
$126K - $215K/yr
As the Senior Principal Medical Writer, you will lead the end-to-end development of complex ... regulatory submission requirements and lifecycle management * Vendor management and remote ...
Billerica, MA · On-site +1
$126K - $215K/yr
As the Senior Principal Medical Writer, you will lead the end-to-end development of complex ... regulatory submission requirements and lifecycle management * Vendor management and remote ...
$14.18 - $18.16
3% of jobs
$18.16 - $22.14
9% of jobs
$26.03 is the 25th percentile. Wages below this are outliers.
$22.14 - $26.11
13% of jobs
$26.11 - $30.09
7% of jobs
$30.09 - $34.07
8% of jobs
$34.07 - $38.05
5% of jobs
The median wage is $39.79 / hr.
$38.05 - $42.02
8% of jobs
$42.02 - $46
16% of jobs
$47.54 is the 75th percentile. Wages above this are outliers.
$46 - $49.98
12% of jobs
$49.98 - $53.96
7% of jobs
$53.96 - $57.93
11% of jobs
$14
$38
$57
| Aspect | Remote Regulatory Medical Writer | Remote Medical Writer |
|---|---|---|
| Credentials | Medical degree, regulatory writing experience, certifications (e.g., RAC) | Medical, scientific, or related degree; writing experience |
| Work Environment | Pharmaceutical/biotech companies, CROs, regulatory agencies | Pharmaceutical, biotech, healthcare, or scientific organizations |
| Industry Usage | Regulatory submissions, INDs, NDAs, safety reports | Research publications, clinical trial documentation, scientific publications |
| Search/Comparison Intent | Regulatory documentation, compliance, submission writing | Scientific writing, research, publication |
The main difference is that Remote Regulatory Medical Writers focus on preparing regulatory documents for drug approvals and compliance, often requiring specific regulatory knowledge and certifications. Remote Medical Writers have a broader scope, including scientific publications and research documentation. Both roles require strong writing skills and relevant scientific backgrounds, but Regulatory Medical Writers specialize in regulatory submissions and compliance processes.
Other
Medical, Dental, Vision, Retirement, PTO
Posted 14 days ago
Lumanity is dedicated to improving patient health by accelerating and optimizing access to medical advances. We partner with life sciences companies around the world to generate evidence to demonstrate the value of their product, translate the science and data into compelling product narratives, and enable commercial decisions that position these products for success in the market. We do this through strategic and complimentary areas of focus: Asset Optimization and Commercialization, Value Access and Outcomes, Medical Strategy and Communications, and Real-World Evidence.
Responsibilities / Position overviewWe are seeking an advanced degree life-sciences professional to serve as a Senior Medical Writer within our Medical Strategy and Communications team, which serves our clients by mobilizing our scientific knowledge to interpret the data and create compelling narratives to guide their medical strategy and through regulatory challenges.
The Senior Medical Writer will ensure high-quality content is developed for a wide range of medical communications projects and deliverables including clinical publications (manuscripts and abstracts), slide decks, scientific platforms, symposia, advisory boards, and training materials. In this role, the Senior Medical Writer has final sign-off authority and will review all deliverables on assigned accounts for technical accuracy, proper incorporation and interpretation of investigator/client data, and overall content and editorial quality. Experience supporting oncology publications accounts is highly desirable.
QualificationsThe ideal candidate will have an advanced degree in a life-sciences field, meticulous attention to detail and the ability to simultaneously work on multiple projects relating to multiple products in various therapeutic areas.
Additional Requirements and Qualifications
We offer our employees a comprehensive benefits package that focuses on what matters to you - health and well-being, personal finances, professional development, and a healthy work/life balance:
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Employment Type: OTHERSourced by ZipRecruiter
Scientific research and development services
1,001 - 5,000 Employees
New York, NY, US
2022