ZipRecruiter

Log In

Incyte
Incyte

32 Incyte Medical Writer Jobs Hiring Near You

next page

Showing results 1-20

All JobsIncyte JobsIncyte Medical Writer Jobs

Incyte Jobs Information

What are the key skills and qualifications needed to thrive as a Medical Writer, and why are they important?

To thrive as a Medical Writer, you need a strong background in life sciences or medicine, excellent written communication skills, and often an advanced degree such as a PhD, MD, or relevant certification. Familiarity with reference management software, medical literature databases, and regulatory guidelines like ICH or GPP is typically required. Attention to detail, the ability to interpret complex data, and collaboration skills set standout professionals apart in this role. These competencies ensure the production of accurate, compliant, and accessible medical documents crucial for regulatory approval, education, and communication in healthcare.

How does a Medical Writer typically collaborate with subject matter experts during a project?

Medical Writers frequently work closely with physicians, researchers, and regulatory specialists to ensure content accuracy and clarity. This collaboration often involves conducting interviews, reviewing scientific data, and incorporating expert feedback into drafts. Building strong professional relationships and maintaining clear communication are key for efficiently resolving technical questions and aligning final documents with project objectives. This teamwork is essential for producing high-quality, compliant materials that meet both scientific and regulatory standards.

What are medical writers?

Medical writers are professionals who create scientific documents related to healthcare, medicine, and the life sciences. They produce materials such as clinical study reports, journal articles, regulatory submissions, and educational content for healthcare professionals or the public. Medical writers must have a strong understanding of medical terminology, research methods, and regulatory guidelines. Their work helps communicate complex scientific information clearly, accurately, and in compliance with industry standards.

What is the difference between Medical Writer vs Clinical Writer?

AspectMedical WriterClinical Writer
CredentialsTypically requires a degree in life sciences, healthcare, or related fields; certifications like AMWA or EMWA are commonSimilar credentials; often holds degrees in life sciences with certifications in clinical research or writing
Work EnvironmentWorks in pharmaceutical, biotech, or healthcare companies, often in offices or remote settingsPrimarily in clinical research organizations, pharmaceutical companies, or hospitals, often in office or remote settings
Industry UsageUsed across pharma, biotech, medical device industries for regulatory, educational, and promotional contentFocused on clinical trial documentation, protocols, and reports within clinical research

Medical Writers and Clinical Writers share similar backgrounds and work environments, often collaborating in healthcare and pharmaceutical sectors. The main difference lies in their focus: Medical Writers create a broad range of medical content, while Clinical Writers specialize in clinical trial documentation and reports.

What other companies are hiring for Medical Writer jobs?
What are the most popular jobs at Incyte?
What are the most popular categories at Incyte?
Infographic showing various Medical Writer job openings at Incyte in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 95% Physical, and 5% Remote job distribution.
Senior/ Executive Medical Director, Medical Lead IAI, Early Clinical Development

Senior/ Executive Medical Director, Medical Lead IAI, Early Clinical Development

Incyte Corporation

Wilmington, DE • On-site

Full-time

Posted 8 days ago

Job description

Overview
Incyte is a global, science-driven biopharmaceutical company recognized for its strong growth and deep commitment to advancing therapies in Hematology, Oncology, and Immunology.
With a diverse and expanding early pipeline, Incyte is shaping the next generation of targeted and immune-based therapies. Our strength lies in our ability to combine scientific insight with clinical execution, transforming discoveries into impactful medicines for patients worldwide.
We are a company in motion, growing, evolving, and investing in early development as a core engine of innovation. At Incyte, every idea begins with science - and every scientist plays a part in shaping what comes next.
The role:
This position is responsible for implementing early clinical development efforts for Incyte's Dermatology, Immunology, Rheumatology products (preclinical candidate nomination through transition to registrational studies)
Duties and Responsibilities
  • Leads development efforts for assets post-candidate selection through first in human trials, including early dose escalation, ph 1-2a translational strategy (proof of mechanism studies) and proof of concept studies in human (ph 1b or 2a).
  • Participates in asset/portfolio strategies and prioritization, internal and external messaging, governance, and cross-functional interface with all key stakeholders, including translational science, clinical pharmacology and pharmacometrics, discovery organization, regulatory and others.
  • Provides medical and scientific expertise for internal cross-functional team members for development of specific, dermatology and immunology agents including discovery scientists, clinical scientists, biostatisticians, pharmacokinetics, pharmacovigilance, and clinical operations.
  • Supports interactions with global regulatory bodies including the FDA, EMA, PMDA and TGA and ethics committees to accomplish tasks related to product development and collaborates with internal regulatory experts and oversee the clinical research plans and sections for Investigational new Drug applications (INDs) and other regulatory documents.
  • Facilitates the development of key internal and external documents pertaining to product development including clinical study protocol, informed consents, CRFs, CSRs, meeting abstracts, scientific journal publications, strategy documents and project plans.
  • Collaborates with external vendors such as CROs, external imaging and laboratory vendors for successful implementation and conduct of early phase clinical studies.
  • Represents Incyte Corporation at key national and international medical and scientific meetings including participation in advisory boards with key opinion leaders.
  • Detects and analyzes emergent issues during early clinical drug development and develops and implements mitigating strategies.
  • Works in partnership with medical affairs and commercial organization for successful launch of future agents.
  • Implements the highest ethical and regulatory standards during the investigation and development of anticancer agents.
  • Provides guidance for successful implementation and accomplishment of investigator-initiated trials related to product development and life cycle management of a compound.
  • Acts as subject matter expert for business development activities

Requirements
  • MD, MD-PhD (or PhD with > 8-year clinical development experience in immunology or dermatology). For MDs a dermatology, rheumatology or clinical immunology/ allergy board certification is preferred.
  • Training in research (wet lab), proven track record of self-directed scientific work (e.g. post doc, peer reviewed publications as first author) preferred. Experience in early drug development required with proven track record of leading clinical pre-clinical candidate to PoC in human
  • Proficient in English, oral and written. Member of at least one professional society (e.g. SID, ACR, AAAAI). Strives for continued medical education in immunology related area.
  • Ability to lead sub-teams and drive projects
  • Track record of business development and due diligence team support
  • Proven record of successful work in diverse, cross-functional teams (co located or not). Willingness to share and coach other Incyte employees within ED and beyond.
  • Desirable preferred behaviour: active listening, higher than average social sensitivity, empathy, willingness to mentor and coach.

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.
We Respect Your Privacy
Learn more at: http://www.incyte.com/privacy-policy
The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate.
During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process here.
You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work.
You can learn more about Incyte's data protection practices here. By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte's data protection officer, and your supervisory authority (if applicable).
Please contact privacy@incyte.com if you have any questions or concerns or would like to exercise your rights.
#LI-MB1

Apply