Senior Medical Writer
NC · Remote
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Join Us as a Senior Medical Writer - Make an Impact at the Forefront of Innovation Provides high-quality medical and scientific ...
NC · Remote
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Join Us as a Senior Medical Writer - Make an Impact at the Forefront of Innovation Provides high-quality medical and scientific ...
NC · Remote
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Join Us as a Senior Medical Writer - Make an Impact at the Forefront of Innovation Provides high-quality medical and scientific ...
$104K - $143K/yr
For the expansion of our team, argenx is looking for a Senior Medical Writer who will provide medical writing support for developing complex clinical, nonclinical, and safety documents for regulatory ...
$104K - $143K/yr
For the expansion of our team, argenx is looking for a Senior Medical Writer who will provide medical writing support for developing complex clinical, nonclinical, and safety documents for regulatory ...
ROLE: The Senior Medical Writer applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of ...
ROLE: The Senior Medical Writer applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of ...
North Haven, CT · On-site +1
We are seeking a Senior Medical Writer to join the Clinical Evaluation team in support of the Core Surgical Innovation business. In this role, the Senior Medical Writer will be responsible for ...
North Haven, CT · On-site +1
We are seeking a Senior Medical Writer to join the Clinical Evaluation team in support of the Core Surgical Innovation business. In this role, the Senior Medical Writer will be responsible for ...
$128K - $210K/yr
We are seeking a Senior Medical Writer to join our Medical Writing team, supporting clinical document delivery across Global Development in a remote work mode. In this role, you will author clinical ...
$128K - $210K/yr
We are seeking a Senior Medical Writer to join our Medical Writing team, supporting clinical document delivery across Global Development in a remote work mode. In this role, you will author clinical ...
The Senior Medical Writer may assist program manager. The role involves collaborating with internal and external clients, supporting and enabling effective and efficient communication that results in ...
The Senior Medical Writer may assist program manager. The role involves collaborating with internal and external clients, supporting and enabling effective and efficient communication that results in ...
North Haven, CT · On-site +1
We are seeking a Senior Medical Writer to join the Clinical Evaluation team in support of the Core Surgical Innovation business. In this role, the Senior Medical Writer will be responsible for ...
North Haven, CT · On-site +1
We are seeking a Senior Medical Writer to join the Clinical Evaluation team in support of the Core Surgical Innovation business. In this role, the Senior Medical Writer will be responsible for ...
The Senior Medical Writer: 1) writes original content for publications activities, and other materials for healthcare professional (HCP) and internal client audiences; 2) demonstrates a command of ...
Quick apply
The Senior Medical Writer: 1) writes original content for publications activities, and other materials for healthcare professional (HCP) and internal client audiences; 2) demonstrates a command of ...
West Chester, PA · On-site +1
The Senior Medical Writer: 1) writes original content for publications activities, and other materials for healthcare professional (HCP) and internal client audiences; 2) demonstrates a command of ...
West Chester, PA · On-site +1
The Senior Medical Writer: 1) writes original content for publications activities, and other materials for healthcare professional (HCP) and internal client audiences; 2) demonstrates a command of ...
The Senior Medical Writer: 1) writes original content for publications activities, and other materials for healthcare professional (HCP) and internal client audiences; 2) demonstrates a command of ...
The Senior Medical Writer: 1) writes original content for publications activities, and other materials for healthcare professional (HCP) and internal client audiences; 2) demonstrates a command of ...
Sr. Medical Writer (Regulatory) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across ...
Sr. Medical Writer (Regulatory) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across ...
Sr. Medical Writer (Regulatory) Syneos Health ® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point ...
Sr. Medical Writer (Regulatory) Syneos Health ® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point ...
Klick is hiring a Senior Medical Writer to develop scientifically accurate, strategically aligned medical communications for life sciences clients. This role partners closely with Medical Strategy ...
Klick is hiring a Senior Medical Writer to develop scientifically accurate, strategically aligned medical communications for life sciences clients. This role partners closely with Medical Strategy ...
Philadelphia, PA · Hybrid
$110K/yr
Klick is hiring a Senior Medical Writer to develop scientifically accurate, strategically aligned medical communications for life sciences clients. This role partners closely with Medical Strategy ...
Philadelphia, PA · Hybrid
$110K/yr
Klick is hiring a Senior Medical Writer to develop scientifically accurate, strategically aligned medical communications for life sciences clients. This role partners closely with Medical Strategy ...
Charleston, WV · On-site
With minimal supervision, authors (writes/edits) high-quality medical writing deliverables (i.e., clinical, safety, regulatory, device, diagnostics, or disclosures documents) across all phases of ...
Charleston, WV · On-site
With minimal supervision, authors (writes/edits) high-quality medical writing deliverables (i.e., clinical, safety, regulatory, device, diagnostics, or disclosures documents) across all phases of ...
Cornelius, NC · On-site +1
The Senior Medical Writer will be responsible for leading and producing high-quality publications and scientific communications, from kick-off to completion. The successful candidate will have ...
Cornelius, NC · On-site +1
The Senior Medical Writer will be responsible for leading and producing high-quality publications and scientific communications, from kick-off to completion. The successful candidate will have ...
The Medical Writer collaborates with members of cross-functional teams to prepare high-quality protocols, investigator brochures, synopses, regulatory documents, clinical publications, and related ...
The Medical Writer collaborates with members of cross-functional teams to prepare high-quality protocols, investigator brochures, synopses, regulatory documents, clinical publications, and related ...
Kennesaw, GA · On-site
Communicate with physicians, vendors, and other medical experts. * Report on adverse events, complaints, and failures associated with the product line identified through the writing process
Kennesaw, GA · On-site
Communicate with physicians, vendors, and other medical experts. * Report on adverse events, complaints, and failures associated with the product line identified through the writing process
Kennesaw, GA · On-site
Communicate with physicians, vendors, and other medical experts. * Report on adverse events, complaints, and failures associated with the product line identified through the writing process
Kennesaw, GA · On-site
Communicate with physicians, vendors, and other medical experts. * Report on adverse events, complaints, and failures associated with the product line identified through the writing process
Boulder, CO · On-site
Degree should be in biological science, English or other relevant area. 5 to 7 years directly related medical writing experience. Outstanding writing, analytical and research skills a must. Ability ...
Boulder, CO · On-site
Degree should be in biological science, English or other relevant area. 5 to 7 years directly related medical writing experience. Outstanding writing, analytical and research skills a must. Ability ...
$35K - $54.3K
17% of jobs
$54.3K - $73.6K
0% of jobs
$73.6K - $93K
4% of jobs
$99K is the 25th percentile. Wages below this are outliers.
$93K - $112.3K
13% of jobs
$112.3K - $131.6K
13% of jobs
The median wage is $135.6K / yr.
$131.6K - $150.9K
18% of jobs
$161.3K is the 75th percentile. Wages above this are outliers.
$150.9K - $170.2K
20% of jobs
$170.2K - $189.5K
6% of jobs
$189.5K - $208.9K
5% of jobs
$208.9K - $228.2K
3% of jobs
$228.2K - $247.5K
1% of jobs
$35K
$137.3K
$247.5K

Full-time
This job post has expired today. Applications are no longer accepted.
7.7
Based on 423 frontline employees who took The Breakroom Quiz
197th of 538 rated manufacturers
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
Join Us as a Senior Medical Writer - Make an Impact at the Forefront of Innovation
Provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. Demonstrates subject matter and therapeutic area expertise. May function as a project lead. Collaborates with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.
What You'll Do:
• Serve as primary author who writes and provides input on routine documents such as Medical Information Response Documents and Questions and Answers.
• May research, write or edit complex clinical and scientific and program level documents, including AMCP dossiers and Infographics.
• Review routine documents prepared by junior team members. May provide training and mentorship for junior writers on document preparation, the use of software for document development, document types, and therapeutic area knowledge.
• Ensure compliance with quality processes and requirements for assigned documents. Provide input on and independently develops best practices, methods and techniques for achieving optimal results, including various client specific processes.
• May function as a project lead or assist with program management activities. Duties could include developing timelines, budgets, forecasts, and contract modifications; tracking deliverable metrics; and representing medical writing team in client meetings.
Education & Experience Requirements:
• Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification; Advanced degree preferred
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).
• Experience working in the pharmaceutical/CRO industry preferred
• Additional qualifications in medical writing or medical information advantageous
Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.
Knowledge, Skills, Abilities:
• Excellent data interpretation and medical writing skills, including grammatical, editorial, and proofreading skills
• Strong project management skills
• Excellent interpersonal skills including problem solving
• Strong negotiation skills
• Excellent oral and written communication skills with strong presentation skills
• Significant knowledge of global, regional, national and other document development guidelines
• In-depth knowledge in a specialty area such as preclinical, therapeutic, regulatory submissions, communications, etc.
• Great judgment and decision-making skills
• Excellent computer skills and skilled with client templates; Good knowledge of document management systems and other relevant applications (e.g. Excel, Outlook)
Working Conditions and Environment:
• Work is performed in an office environment.
• Exposure to electrical office equipment.
• Occasional drives to site locations with occasional travel both domestic and international.
• Long, varied hours required occasionally.
Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.
Apply today to help us deliver tomorrow’s breakthroughs.
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Biotechnology research and development
10,000+ Employees
Waltham, MA, US
1956