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Vp Remote Medical Writing Jobs in Rochester, NY (NOW HIRING)

micro1 AI

Medical Writing Manager

Rochester, NY · Remote

$50 - $80/hr

Role Title: Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project

micro1 AI

Medical Billing Specialist

Rochester, NY · Remote

$50 - $80/hr

Role Title: Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project

Bayer

National Account Dir Health Systems

Rochester, NY · On-site +1

$177K - $266K/yr

At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where 'Health for all Hunger for none' is no longer a dream, but a real possibility. We're doing

New

Bayer

National Account Dir Health Systems

Webster, NY · On-site +1

$177K - $266K/yr

At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where 'Health for all Hunger for none' is no longer a dream, but a real possibility. We're doing

New

Deloitte

PAM Senior Manager

Rochester, NY · On-site +1

$109K - $148K/yr

Our Deloitte Cyber team understands the unique challenges and opportunities businesses face in cybersecurity. Join our team to deliver powerful solutions to help our clients navigate the

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All JobsVp Medical Writing JobsVp Remote Medical Writing JobsVp Remote Medical Writing Jobs in Rochester, NY

Vp Remote Medical Writing information

See Rochester, NY salary details

$99.7K

$181K

$362.1K

How much do vp remote medical writing jobs pay per year?

As of Sep 13, 2026, the average yearly pay for vp remote medical writing in Rochester, NY is $181,047.00, according to ZipRecruiter salary data. Most workers in this role earn between $142,100.00 and $197,300.00 per year, depending on experience, location, and employer.

What is a VP of remote medical writing?

A VP of Remote Medical Writing is a senior executive responsible for overseeing and managing medical writing teams and projects from a remote location. Their primary duties include setting strategic direction, ensuring high-quality scientific content, maintaining regulatory compliance, and coordinating with cross-functional teams such as clinical, regulatory, and marketing. They also play a key role in talent management, process improvement, and client relationship management within medical communications organizations. This leadership role requires extensive experience in medical writing, a deep understanding of healthcare regulations, and strong organizational and communication skills.

How does a VP of remote medical writing typically collaborate with cross-functional teams while working remotely?

As a VP of Remote Medical Writing, you will frequently collaborate with regulatory, clinical, and publication teams through virtual meetings, shared project management platforms, and regular communication channels. You’ll be responsible for leading and mentoring a distributed team of writers while ensuring high standards and consistency across all deliverables. Strong digital communication and organizational skills are essential, as you will need to manage multiple projects and deadlines, coordinate feedback, and maintain alignment with broader organizational goals, all within a remote work environment.

What are the key skills and qualifications needed to thrive as a VP of remote medical writing, and why are they important?

To thrive as a VP of Remote Medical Writing, you need advanced expertise in medical writing, regulatory documentation, and leadership, typically supported by a life sciences degree and extensive industry experience. Familiarity with document management systems, ICH-GCP guidelines, and tools like EndNote or reference managers is essential, along with certifications such as AMWA or EMWA. Strategic thinking, excellent communication, and the ability to lead distributed teams are critical soft skills for this senior role. These competencies ensure the production of high-quality, compliant documents and effective team performance in a remote environment.

What is the difference between Vp Remote Medical Writing vs Medical Writing Manager?

AspectVp Remote Medical WritingMedical Writing Manager
CredentialsTypically requires advanced degrees (PhD, MD, PharmD) and extensive medical writing experienceUsually requires a bachelor's or master's degree in life sciences or related field, with several years of medical writing experience
Work EnvironmentRemote or hybrid, often within pharmaceutical or biotech companies, overseeing global projectsPrimarily office-based or hybrid, managing medical writing teams within pharmaceutical or CRO settings
ResponsibilitiesStrategic leadership, project oversight, client communication, high-level content reviewTeam management, project coordination, quality control, ensuring regulatory compliance

The Vp Remote Medical Writing role focuses on strategic leadership and high-level oversight, often remotely, while the Medical Writing Manager handles team management and project execution. Both roles require strong medical writing credentials but differ in scope and seniority.

What are popular job titles related to Vp Remote Medical Writing jobs in Rochester, NY?

For Vp Remote Medical Writing jobs in Rochester, NY, the most frequently searched job titles are:

What job categories do people searching Vp Remote Medical Writing jobs in Rochester, NY look for?

The top searched job categories for Vp Remote Medical Writing jobs in Rochester, NY are:

What cities near Rochester, NY are hiring for Vp Remote Medical Writing jobs?

Cities near Rochester, NY with the most Vp Remote Medical Writing job openings:

Vp Remote Medical Writing jobs near you
Infographic showing various Vp Remote Medical Writing job openings in Rochester, NY as of September 2026, with employment types broken down into 1% As Needed, 76% Full Time, 16% Part Time, and 7% Contract. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $181,047 per year, or $87 per hour.

Medical Writing Manager

Rochester, NY • Remote

micro1 AI
Software Development • 11 - 50 employees
Learn more about micro1 AIexternal

$50 - $80/hr

Part-time

Re-posted 10 days ago

Job description

Role Title: Medical Writer / Clinical Document Author


Role Type: Contractor


Location: Remote


micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer’s project focused on developing advanced AI-assisted writing tools for clinical documentation. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development.
  2. Apply expert judgment to assess whether AI-generated content fulfills clinical template and structural requirements, including ICH E3 organization, section sequencing, cross-referencing, and appendix management.
  3. Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion, and conclusions, distinguishing true scientific or interpretive errors from stylistic differences.
  4. Trace narrative claims to source records—tables, figures, listings, and protocols—to verify that all assertions are appropriately supported.
  5. Provide clear and structured written rationales for each assessment, enabling precise diagnosis and improvement of AI model behavior.
  6. Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI.


Preferred Qualifications

  1. Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant.
  2. Direct experience independently authoring or leading the authoring of full Clinical Study Reports, beyond summaries or partial contributions.
  3. Fluency with ICH E3 and conventions for periodic safety documentation (ICH E2F, ICH E2C) and eCTD placement.
  4. Demonstrated ability to read and interpret TFLs and protocol documents, identifying where narrative diverges from source data.
  5. Exceptional written and verbal communication skills, especially in providing structured, actionable feedback on clinical content.
  6. Advanced degree in life sciences, pharmacy, or medicine (PhD, PharmD, MD, MSc), or equivalent depth of authoring experience.
  7. Experience across multiple clinical phases and therapeutic areas; oncology and haematology expertise is especially valued.


Join our customer's team and leverage your authoring expertise to help design the next generation of AI-assisted clinical documentation solutions. This high-bar role offers you the chance to shape how tomorrow's writing teams draft and review regulatory documents — through your expert input, judgment, and real-world experience.

Apply