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Remote Senior Medical Editor Jobs in Raleigh, NC

Workplace Options

Proposal Specialist

Raleigh, NC · Remote

Remote Required Languages: English Required Experience: 5+ years Hours: 10am- 6pm EST Salary: 60 ... You will also be responsible for assigning responsibilities, monitoring working drafts, editing and ...

Workplace Options

Proposal Specialist

Raleigh, NC · On-site +1

Remote Required Languages: English Required Experience: 5+ years Hours: 10am- 6pm EST Salary: 60 ... You will also be responsible for assigning responsibilities, monitoring working drafts, editing and ...

Higharc

Residential Drafter

Durham, NC · Remote

Lead implementation of builder homes into the Higharc Editor, managing task progress and gaps ... Remote work means more time with family, less time commuting, and the flexibility to blend work and ...

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All JobsMedical Editor JobsRemote Senior Medical Editor JobsRemote Senior Medical Editor Jobs in Raleigh, NC

Remote Senior Medical Editor information

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$36K

$80.8K

$117.1K

How much do remote senior medical editor jobs pay per year?

As of Sep 14, 2026, the average yearly pay for remote senior medical editor in Raleigh, NC is $80,790.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,200.00 and $101,600.00 per year, depending on experience, location, and employer.

What is the difference between Remote Senior Medical Editor vs Remote Medical Writer?

AspectRemote Senior Medical EditorRemote Medical Writer
Required CredentialsMedical degree or equivalent, editorial certificationsMedical or scientific degree, writing experience
Work EnvironmentEditorial teams, publishing companies, healthcare agenciesResearch teams, pharmaceutical companies, healthcare publishers
Employer & Industry UsageUsed in medical publishing, pharma, biotechUsed in clinical research, regulatory, pharma
Common Search & ComparisonOften compared for editing vs writing roles in medical communication

The Remote Senior Medical Editor primarily focuses on reviewing and refining medical content for accuracy and clarity, often overseeing editing teams. In contrast, the Remote Medical Writer is responsible for creating original medical documents, such as manuscripts, regulatory submissions, or educational materials. Both roles require strong medical knowledge and communication skills, but their core functions differ—editing versus writing. Understanding these distinctions helps professionals choose the role that best aligns with their skills and career goals.

What are popular job titles related to Remote Senior Medical Editor jobs in Raleigh, NC?

For Remote Senior Medical Editor jobs in Raleigh, NC, the most frequently searched job titles are:

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Remote Senior Medical Editor jobs near you

VP, Medical Science & Strategy - Cardiovascular(Remote U.S)

Raleigh, NC • On-site, Remote

Thermo Fisher Scientific
Biotechnology Research and Development • 10K+ employees
Learn more about Thermo Fisher Scientificexternal

Full-time

Re-posted 13 days ago

Key responsibilities

  • Support the development of strategies and provide input on regulatory, drug class, protocol, and indication considerations for proposals and bid defenses.

  • Engage with clients, internal teams, and external stakeholders to support clinical research activities, including strategic alliance development and client engagement.

  • Provide therapeutic and developmental expertise to internal teams, including training, guidance during clinical trials, and review of regulatory documents.

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 432 frontline employees who took The Breakroom Quiz

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
*Must be legally authorized to work in the United States without sponsorship.
*Must be able to pass a comprehensive background check, which includes a drug screening.
The position requires proven abilities to drive both strategic and measurable business outcomes. The incumbent's cardiovascular diseases track record expertise is required to be extensive and ensure recognition as peer of their Pharmaceutical Industry equivalents. This position is playing a key part in the future success of the PPD clinical research business of Thermo Fisher Scientific, as it seeks to continue its track record of successful growth and expand Industry leading position in the cardiovascular diseases field. Medical Science & Strategy physicians are subject matter experts who support sales for proposals and bid defenses, engaging clients senior medical / scientific leadership in discussions and training internal staff on medical and therapeutic requirements of the proposals.
The role comprises four major functions:
First, the incumbent is responsible for ensuring the highest possible quality of input into significant requests for proposals (RFPs), including:
  • Development strategy and regulatory issues
  • Drug class issues
  • Protocol and indication considerations, including safety
  • Team education on indication
  • Interactions with client's physicians and / or client area indication leaders prior to and during bid defenses
  • Identifying business opportunities for the PPD clinical research business

Secondly, the incumbent is responsible for supporting outstanding input into other areas of the PPD clinical research business activities, including:
  • Pro-active client engagement: peer-to-peer interactions with therapeutic area leaders and senior directors of companies whose portfolio contains drugs of business interest
  • Strategic alliance development & support
  • Client governance and advisory boards
  • Through PPD's consulting practice, the incumbent will provide Industry gold standard product development plans, and top-level design of clinical trial protocols that are required in the development plan.

Thirdly, the incumbent will be responsible for providing therapeutic and developmental expertise to internal teams, including:
  • Indication specific training for clinical teams
  • Guidance during clinical trials executions
  • Investigator Brochure, clinical study report, NDA / MAA clinical packages development, and other regulatory briefing documents authoring and review
  • Contribute to design and reporting of feasibility studies
  • Liaise with investigators and KOLs
  • Mentor and supervise clinical scientists

Finally, the incumbent will participate in multidisciplinary teams and working groups to contribute to innovative initiatives based on their specific knowledge, expertise and interest.
Minimum Qualifications:
  • MD required; board certification preferred.
  • At least 7 years of experience in the pharmaceutical industry leading cardiovascular clinical development programs, including advancement of at least one asset from discovery through registration.
  • Active medical license preferred but not required.

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills and Abilities:
  • Able to work in a matrix organization.
  • Able to demonstrate the following key high-level high-performance behaviors: decisive, customer driven, flexible thinking, smart-risk taking and continuous improvement.
  • Leads, influences and motivates staff within and across departments.
  • Strong in presenting and communicating complex information clearly.
  • Able to deal with sensitive and confidential issues.
  • Possesses a "can do" attitude and is capable of implementing and following through on activities / projects.
  • Proficient in spoken and written English.
  • Flexibility to travel domestically and internationally

What we offer:
  • Full time position
  • Competitive salary and benefits
  • Work diversity, exposure to several assets in different stages of clinical development from several clients
  • Mentorship and training
  • Exciting work environment

About PPD clinical research business of Thermo Fisher Scientific Our mission is to enable our customers to make the world healthier, cleaner and safer. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Apply today!

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