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Associate Director Medical Writing Jobs in Raleigh, NC

IQVIA

Medical Director, Cardiology

Durham, NC · Remote

The Associate Medical Director / Medical Director will provide medical, clinical and scientific ... both written and spoken). * Robust and current knowledge of scientific, clinical, regulatory ...

IQVIA

Medical Director, Cardiology

Durham, NC · Remote

The Associate Medical Director / Medical Director will provide medical, clinical and scientific ... both written and spoken). * Robust and current knowledge of scientific, clinical, regulatory ...

IQVIA

Medical Director, Cardiology

Durham, NC · Remote

The Associate Medical Director / Medical Director will provide medical, clinical and scientific ... both written and spoken). * Robust and current knowledge of scientific, clinical, regulatory ...

IQVIA, Inc.

Medical Director, Cardiology

Durham, NC · On-site

The Associate Medical Director / Medical Director will provide medical, clinical and scientific ... both written and spoken). * Robust and current knowledge of scientific, clinical, regulatory ...

IQVIA

Medical Director, Cardiology

Durham, NC · Remote

The Associate Medical Director / Medical Director will provide medical, clinical and scientific ... both written and spoken). * Robust and current knowledge of scientific, clinical, regulatory ...

IQVIA, Inc.

Medical Director, Cardiology

Durham, NC · On-site

The Associate Medical Director / Medical Director will provide medical, clinical and scientific ... both written and spoken). * Robust and current knowledge of scientific, clinical, regulatory ...

IQVIA

Associate Director, Metrology

Durham, NC · On-site

$89K - $206K/yr

Internal We are seeking an Associate Director, Metrology to join IQVIA Laboratories. We hire ... innovative medical treatments to help improve patient outcomes and population health worldwide.

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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.

Oncology Scientific Lead, Med Com (Associate Scientific Dir)

410 ICR United States USA

Raleigh, NC • Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 29 days ago

Job description

Scientific Lead - Medical Communications

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


ICON Global Medical Communications (GMC) is looking for a passionate, and inspiring Scientific Lead to join our team. As a Scientific Lead you will build on the responsibilities of a Sr. Medical Writer and take on additional project-level content development and management responsibilities. This role encompasses high-level writing, peer-review of project deliverables, strategic support and client engagement as determined by the respective aligned account leaders.

Your primary responsibility will be independent approval of scientific/clinical content for assigned projects/tasks.Your oversight will include review of assigned materials for accuracy and quality, mentoring and developing junior writing staff, and contributing scientific and therapeutic insights. The Scientific Lead will work closely with the Scientific Manager to support members of the client account team as directed.

This person should have prior experience with background researching, developing, and high-quality writing for the diverse array of deliverables within medical publications and medical communications.

What You'll Be Doing:

Content oversight and quality control responsibilities are including but not limited to:

  • Review work of other internal writers, including junior medical writers
  • Product/therapy area information and strategic insight pertinent to the assigned projects
  • Fact checking assigned manuscripts
  • Collaboration with the Scientific Manager and account managers to help ensure adherence to agreed-upon timelines
  • Helping to oversee all aspects of project development from initiation to completion, including escalating issues with financial impacts

Scientific/medical writing and content-development support:

  • Writing manuscripts, posters, abstracts, slide decks, and/ or other deliverables requiring scientific/medical writing support
  • Identify and obtain required/helpful background materials, including from client
  • Collaborating with editorial support staff to provide necessary background and technical information
  • Participate in onboarding and mentoring of new and junior medical writers
  • Conduct background research and writing support for new business proposals and organic growth opportunities

What you need:

  • Advanced degree, preferably PhD but PharmD and MD may also be considered
  • Prior experience in a medical publications/medical communications agency
  • Minimum of 4–5 years’ experience of high-level content development and management actives in the medical communication agency setting
  • 3 years as a Senior Medical Writer, strongly preferred
  • CMPP™/MAPPS Certification, great to have
  • Demonstrable history of relevant high-level writing support and review (e.g, while at a medical communications agency), including proficiency with ICMJE and GPP guidelines; reviewing and interpreting scientific and technical journal content; knowledge of diverse prescribed styles and formats
  • People management and client relationship skills preferred
  • Ability to work efficiently with network directories/databases
  • Familiarity and ability to work with industry standard resources (e.g., PubMed/Medline, clinicaltrials.gov, various market intelligence/data analytic providers, etc)
  • Ability to work with cross-functional teams (e.g., editorial/library services, graphics/digital services, presentations support, etc)

#LI-KM3

#LI-REMOTE


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply