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Internship Medical Writing Jobs in Delaware (NOW HIRING)

Danaher

By submitting your interest, you'll be among the first to know when internship opportunities open ... Writing and debugging code in languages such as C#, Java, Python, or C++ * Participating on an ...

Danaher

Software Engineer Internships

Smyrna, DE

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Danaher

Software Engineer Internships

Milford, DE

By submitting your interest, you'll be among the first to know when internship opportunities open ... Writing and debugging code in languages such as C#, Java, Python, or C++ * Participating on an ...

Danaher

Software Engineer Internships

Milford, DE · On-site

By submitting your interest, you'll be among the first to know when internship opportunities open ... Writing and debugging code in languages such as C#, Java, Python, or C++ * Participating on an ...

Danaher

Software Engineer Internships

Wilmington, DE

By submitting your interest, you'll be among the first to know when internship opportunities open ... Writing and debugging code in languages such as C#, Java, Python, or C++ * Participating on an ...

Danaher

By submitting your interest, you'll be among the first to know when internship opportunities open ... Writing and debugging code in languages such as C#, Java, Python, or C++ * Participating on an ...

Danaher

Software Engineer Internships

Dover, DE

By submitting your interest, you'll be among the first to know when internship opportunities open ... Writing and debugging code in languages such as C#, Java, Python, or C++ * Participating on an ...

Danaher

Software Engineer Internships

Dover, DE · On-site

By submitting your interest, you'll be among the first to know when internship opportunities open ... Writing and debugging code in languages such as C#, Java, Python, or C++ * Participating on an ...

Danaher

By submitting your interest, you'll be among the first to know when internship opportunities open ... Writing and debugging code in languages such as C#, Java, Python, or C++ * Participating on an ...

Danaher

Software Engineer Internships

Middletown, DE · On-site

By submitting your interest, you'll be among the first to know when internship opportunities open ... Writing and debugging code in languages such as C#, Java, Python, or C++ * Participating on an ...

Danaher

Software Engineer Internships

Smyrna, DE · On-site

By submitting your interest, you'll be among the first to know when internship opportunities open ... Writing and debugging code in languages such as C#, Java, Python, or C++ * Participating on an ...

Danaher

By submitting your interest, you'll be among the first to know when internship opportunities open ... Writing and debugging code in languages such as C#, Java, Python, or C++ * Participating on an ...

Danaher

Software Engineer Internships

Wilmington, DE · On-site

By submitting your interest, you'll be among the first to know when internship opportunities open ... Writing and debugging code in languages such as C#, Java, Python, or C++ * Participating on an ...

Danaher

Software Engineer Internships

Middletown, DE

By submitting your interest, you'll be among the first to know when internship opportunities open ... Writing and debugging code in languages such as C#, Java, Python, or C++ * Participating on an ...

Danaher

Software Engineer Internships

Newark, DE · On-site

By submitting your interest, you'll be among the first to know when internship opportunities open ... Writing and debugging code in languages such as C#, Java, Python, or C++ * Participating on an ...

Danaher

By submitting your interest, you'll be among the first to know when internship opportunities open ... Writing and debugging code in languages such as C#, Java, Python, or C++ * Participating on an ...

Danaher

By submitting your interest, you'll be among the first to know when internship opportunities open ... Writing and debugging code in languages such as C#, Java, Python, or C++ * Participating on an ...

Danaher

By submitting your interest, you'll be among the first to know when internship opportunities open ... Writing and debugging code in languages such as C#, Java, Python, or C++ * Participating on an ...

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Internship Medical Writing information

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How much do internship medical writing jobs pay per hour?

As of Aug 5, 2026, the average hourly pay for internship medical writing in Delaware is $15.56, according to ZipRecruiter salary data. Most workers in this role earn between $12.50 and $17.55 per hour, depending on experience, location, and employer.

What are medical writing internship opportunities?

Medical writing internship opportunities are for students who want to gain experience in the field of medical writing. Your duties can depend on the details of the internship program and the area in which you wish to specialize. A student intern works under the supervision of medical staff or professional medical writers. Your responsibilities can include creating documents for medical device or pharmaceutical companies or performing writing of reports and articles for researchers. As an intern, you often perform document searches or background research to aid in an organization's clinical writing efforts. You may be asked to complete unrelated tasks as well, such as making coffee runs.

What is an internship in medical writing?

An internship in medical writing is a temporary position designed to provide hands-on experience in creating scientific documents related to medicine and healthcare. Interns typically work under the supervision of experienced medical writers, assisting with tasks such as writing, editing, and reviewing clinical study reports, regulatory documents, scientific articles, and patient education materials. This role helps interns develop a deep understanding of medical terminology, guidelines, and the drug development process, while also improving their writing and communication skills. Medical writing internships are often sought by students or recent graduates in life sciences or related fields who are interested in a career that combines science and communication.

What types of projects and tasks can I expect to work on during a medical writing internship?

As a medical writing intern, you will typically assist with drafting, editing, and reviewing various documents such as clinical study reports, regulatory submissions, patient information leaflets, and scientific manuscripts. You'll often collaborate closely with senior medical writers, researchers, and subject matter experts to ensure accuracy and clarity. Interns may also help with literature searches, data presentation, and preparing materials for conferences or publications. This hands-on experience provides valuable insight into the medical communications field and helps develop both technical writing and teamwork skills.

What are the key skills and qualifications needed to thrive as an internship medical writer, and why are they important?

To thrive as an Internship Medical Writer, you need a strong background in life sciences or healthcare, excellent written communication skills, and attention to detail, often supported by a relevant degree or ongoing studies. Familiarity with referencing tools like EndNote, document management systems, and basic knowledge of regulatory writing standards is beneficial. Strong organizational skills, adaptability, and the ability to work collaboratively are standout soft skills in this role. These competencies are crucial for producing accurate, clear, and compliant medical documents that meet industry standards and support effective communication within teams.

What is the difference between Internship Medical Writing vs Medical Writing?

AspectInternship Medical WritingMedical Writing
CredentialsTypically students or recent graduates; basic knowledge of medical/scientific conceptsRequires relevant degrees (e.g., life sciences, medicine), certifications often preferred
Work EnvironmentInternship programs, often in pharmaceutical or biotech companies, research institutionsFull-time roles in pharma, biotech, or medical communication agencies
ResponsibilitiesAssisting with document drafting, research, learning industry standardsAuthoring clinical study reports, regulatory documents, publications

Internship Medical Writing is an entry-level position designed for learning and skill development, often held by students or recent graduates. Medical Writing is a professional role requiring more experience and expertise in creating complex scientific documents. Both roles are essential in the healthcare industry, but internships serve as a stepping stone toward full-time medical writing careers.

More about Internship Medical Writing jobs
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What cities in Delaware are hiring for Internship Medical Writing jobs? Cities in Delaware with the most Internship Medical Writing job openings:
Internship Medical Writing jobs near you

Manager, Global Risk Management & Safety Surveillance Scientist

Incyte Corporation

Wilmington, DE • On-site

Full-time

Re-posted yesterday

Job description

Overview
A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity
Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia.
The job is based in Wilmington Delaware, US. (Minimum 3 days per week in the office. Local candidates or those willing to relocate only).
Job Summary (Primary function)
This Global Risk Management & Safety Surveillance (GRMSS) Scientist collaborates with the GRMSS Physician to characterize the evolving clinical and post-marketing safety profiles for Incyte investigational drugs and/or products, based on analysis of aggregate data sets from internal or external sources and the medical literature. This entails drafting, reviewing, and refining portions of periodic aggregate safety reports (including DSURs, RMPs, and PBRERs), IB/RSI updates, safety-related product label updates, and responses to health authority requests for information. The GRMSS Scientist performs the signal detection activities and review process for clinical and post-marketing data, including signal detection, evaluation, and verification; potential sources of data for signal detection include Incyte, external marketing partners, or contracted business entities. The Scientist in this position documents signal detection activities and communicates appropriate summaries to internal stakeholders and external partners.
Qualifications
Education
  • Healthcare degree (e.g., BSN, CRNP, Pharm.D.) preferred (or relevant scientific degree buttressed by industry experience).
  • Oncology Nurse Practitioners, Physician Assistants, and Pharmacists seeking to transition into the pharmaceutical industry are encouraged to apply.
  • Willingness to travel (less than 5%) to domestic conferences, as applicable, with reasonable accommodations made for individuals with disabilities.

Experience
  • 0-2 years of relevant experience.
  • Experience may be gained through clinical practice, fellowship, residency, research, internships, or industry roles.
  • Recent graduates, fellows, residents, and early-career professionals are encouraged to apply.
  • Prior pharmaceutical, biotechnology, pharmacovigilance, or drug safety experience is beneficial but not required.

Knowledge & Skills
  • Strong written and verbal communication skills.
  • Interest in drug safety, risk management, pharmacovigilance, and drug development.
  • Strong attention to detail and ability to work collaboratively across functions.
  • Willingness to learn global pharmacovigilance regulations, safety surveillance activities, and risk management processes.

Essential Functions of the Job (Key responsibilities)
  • Provide overall support to the GRMSS Physicians for global risk management and safety surveillance activities.
  • Support/contribute to the discussions on risk management safety strategies to internal stakeholders (e.g., Clinical Development, Medical Affairs, Regulatory Affairs, Quality Assurance, Commercial, Translational & Experimental Medicine, and Legal).
  • Contribute to preparedness for regulatory authority inspection and internal audits of Incyte Pharmacovigilance by following standard operation procedures and processes.
  • Participate in internal safety process improvements and updates.
  • Support the GRMSS Physician in evaluating safety data to compile reference safety information for Incyte products, included in the Investigator Brochures, Core Data Sheets, and regional labels.
  • Participate in the review of integrated summaries of safety, clinical overviews, and other registration documents (e.g., for new and supplemental NDAs and/or ex-US new drug submissions for late-phase drug development candidates and marketed products) in collaboration with the GRMSS team, including professionals from Clinical Development, Medical Writing, Statistics, and Regulatory Affairs.
  • In collaboration with the GRMSS Physician/Scientist, support the preparation of Aggregate Reports (DSURs, PSURS, PADERS, etc.) for Incyte clinical trial programs and marketed products.
  • Provide support as needed to the GRMSS Physician in reviewing periodic literature for new and important information regarding Incyte products.
  • Support the GRMSS Physician/Scientist in the preparation of initial Risk Management Plans (RMPs) and subsequent updates throughout the lifecycle of a medicinal product.
  • Perform drug signal management activities, including the drafting of signal evaluation reports for Incyte's portfolio of investigational and marketed products.
  • Collaborate with GRMSS Physician in the development of clinical trial and post-marketing risk management safety strategies.
  • Support GRMSS Medical Professional and coordinate/lead Safety Management Team meetings.

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.
Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.
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.
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