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Associate Director Medical Writing Jobs in Raleigh, NC

micro1 AI

Medical Billing Specialist

Raleigh, NC · Remote

$50 - $80/hr

Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience independently authoring or leading the authoring of full Clinical ...

micro1 AI

Medical Billing Specialist

Durham, NC · Remote

$50 - $80/hr

Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience independently authoring or leading the authoring of full Clinical ...

micro1 AI

Medical Billing Specialist

Cary, NC · Remote

$50 - $80/hr

Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience independently authoring or leading the authoring of full Clinical ...

Jobtailor

Senior Director, Clinical Development

Cary, NC · On-site

$120 - $190/hr

Write, edit, and review medical and scientific elements of both internal and external facing documents inclusive of clinical research * Manage Key Opinion Leader and Medical Advisory Board ...

AT&T

Associate Director-Sales Prof Svcs ATC

Durham, NC · On-site

$155K - $233K/yr

Medical/Dental/Vision coverage * 401(k) plan * Tuition reimbursement program * Paid Time Off and ... Our Associate Director-Sales Prof Svcs ATC jobs earn between $139,100.00 - $250,400.00 + commission ...

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All JobsAssociate Medical Writing JobsAssociate Director Medical Writing JobsAssociate Director Medical Writing Jobs in Raleigh, NC

Associate Director Medical Writing information

See Raleigh, NC salary details

$73.4K

$160.2K

$255.2K

How much do associate director medical writing jobs pay per year?

As of Aug 14, 2026, the average yearly pay for associate director medical writing in Raleigh, NC is $160,196.00, according to ZipRecruiter salary data. Most workers in this role earn between $118,100.00 and $194,400.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an associate director medical writing?

To thrive as an Associate Director Medical Writing, you need advanced knowledge of clinical research, regulatory requirements, and scientific writing, typically supported by a life sciences degree and extensive medical writing experience. Familiarity with document management systems, regulatory submission platforms, and guidelines such as ICH and FDA is crucial. Outstanding leadership, attention to detail, and strong communication skills help manage teams and ensure clarity in complex scientific documents. These competencies are vital for producing high-quality regulatory documents that meet industry standards and support successful drug development.

How does an associate director medical writing typically collaborate with cross-functional teams during the drug development process?

As an Associate Director of Medical Writing, you will frequently collaborate with regulatory affairs, clinical development, biostatistics, and medical affairs teams to ensure the accuracy and compliance of regulatory documents. This role often involves leading writing teams, managing timelines, and synthesizing input from subject matter experts to produce high-quality submissions. Effective communication and project management skills are crucial, as you’ll coordinate review cycles, address feedback, and ensure consistency across documents. These cross-functional interactions are essential for meeting regulatory requirements and supporting successful drug submissions.

What does an associate director medical writing do?

An Associate Director of Medical Writing leads a team of medical writers in creating and reviewing scientific documents for regulatory submissions, publications, and clinical studies. They ensure accuracy, compliance with guidelines, and high-quality content while managing timelines and collaborating with cross-functional teams such as clinical, regulatory, and biostatistics departments. This role often involves mentoring junior writers, overseeing project workflows, and providing strategic input on document development. Their work plays a critical role in the successful communication of clinical research findings and regulatory submissions.

Is there a demand for associate director medical writing?

The role of associate director medical writing is in high demand due to the growth of the pharmaceutical and biotech industries, which require skilled professionals to develop regulatory documents, clinical study reports, and scientific publications. Candidates with strong writing skills, industry knowledge, and familiarity with regulatory guidelines like ICH and FDA are sought after, especially in organizations emphasizing compliance and quality. The demand is expected to remain steady as drug development and approval processes continue to expand globally.

What is the difference between Associate Director Medical Writing vs Medical Writer?

AspectAssociate Director Medical WritingMedical Writer
QualificationsAdvanced degree (MD, PhD, PharmD), extensive experience in medical writingBachelor's or Master's degree in life sciences or related field
Work EnvironmentLeads teams, manages projects, collaborates with cross-functional teamsPrepares clinical and regulatory documents, works under supervision
ResponsibilitiesStrategic oversight, team management, high-level reviewDrafts and edits clinical/regulatory documents, supports project teams

The Associate Director Medical Writing typically holds advanced degrees and has leadership responsibilities, overseeing teams and strategic projects. Medical Writers usually have relevant scientific degrees and focus on producing high-quality documents under supervision. The roles differ mainly in scope, responsibility, and level of experience required.

What are popular job titles related to Associate Director Medical Writing jobs in Raleigh, NC?

For Associate Director Medical Writing jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Associate Director Medical Writing jobs in Raleigh, NC look for?

The top searched job categories for Associate Director Medical Writing jobs in Raleigh, NC are:

Associate Director Medical Writing jobs near you
Infographic showing various Associate Director Medical Writing job openings in Raleigh, NC as of August 2026, with employment types broken down into 91% Full Time, and 9% Contract. Highlights an 49% In-person, 14% Hybrid, and 37% Remote job distribution, with an average salary of $160,196 per year, or $77 per hour.

Medical Billing Specialist

micro1 AI

Raleigh, NC • Remote

$50 - $80/hr

Part-time

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