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Associate Medical Writer Jobs in Delaware (NOW HIRING)

Walmart

Auto Care Center Service Writer

Camden, DE · On-site

$15 - $28/hr

Health benefits include medical, vision and dental coverage. Financial benefits include 401(k) ... part-time associates in Walmart and Sam's Club facilities. Programs range from high school ...

Adecco

Manufacturing Associate

Milford, DE

$15 - $16/hr

Ability to read and follow written, verbal, and diagram-based instructions, including safety ... for our associates include medical, dental, vision, life insurance, short-term disability ...

Adecco

Manufacturing Associate

Milford, DE

$15 - $16/hr

Ability to read and follow written, verbal, and diagram-based instructions, including safety ... for our associates include medical, dental, vision, life insurance, short-term disability ...

Elevance Health

Manager I Medical Mgmt

Wilmington, DE · On-site

$108K - $162K/yr

This role requires associates to be in-office 3 days per week, fostering collaboration and ... Strong oral, written and interpersonal communication skills, problem-solving skills, facilitation ...

TidalHealth

Medical Laboratory Technician II

Seaford, DE · On-site

$24.41 - $37.84/hr

... written policies and procedures under the supervision of the appropriate Section Head. The MLT II ... Associate Degree in Medical Laboratory Technology or a related biological science and eligible for ...

TidalHealth

Medical Laboratory Technician II

Seaford, DE · On-site

$24.41 - $37.84/hr

... written policies and procedures under the supervision of the appropriate Section Head. The MLT II ... Associate Degree in Medical Laboratory Technology or a related biological science and eligible for ...

Express

Sales Associate

Rehoboth Beach, DE · On-site

$13.50 - $18.50/hr

... written communication skills specifically with customers, sales leadership team and associates ... Medical, pharmacy, dental and vision coverage 401(k) and Roth 401(k) with Company match Merchandise ...

Express

Sales Associate

Rehoboth Beach, DE · On-site

$13.50 - $18.50/hr

Strong verbal and written communication skills specifically with customers, sales leadership team ... Medical, pharmacy, dental and vision coverage * 401(k) and Roth 401(k) with Company match

Express & Bonobos

Sales Associate

Rehoboth Beach, DE

$13.50 - $18.50/hr

Strong verbal and written communication skills specifically with customers, sales leadership team ... Medical, pharmacy, dental and vision coverage * 401(k) and Roth 401(k) with Company match

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All JobsAssociate Medical Writer JobsAssociate Medical Writer Jobs in Delaware

Associate Medical Writer information

See Delaware salary details

$14

$38

$57

How much do associate medical writer jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for associate medical writer in Delaware is $38.67, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.85 per hour, depending on experience, location, and employer.

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

To thrive as an Associate Medical Writer, you need a solid background in life sciences, strong writing abilities, and attention to detail, often supported by a relevant degree such as biology, pharmacy, or medicine. Familiarity with referencing tools (e.g., EndNote), medical literature databases (e.g., PubMed), and proficiency in Microsoft Office are typically required. Excellent communication, time management, and the ability to interpret complex scientific data set standout candidates apart. These skills ensure that scientific information is accurately and clearly communicated to varied audiences, supporting effective healthcare and regulatory decision-making.

What are some common challenges faced by associate medical writers during their first year on the job?

In their first year, Associate Medical Writers often find it challenging to quickly adapt to diverse writing styles and strict formatting guidelines required by different clients or regulatory bodies. Balancing tight deadlines while ensuring scientific accuracy and compliance can also be demanding, especially when juggling multiple projects. Additionally, learning to effectively collaborate with multidisciplinary teams—including clinicians, researchers, and senior writers—requires strong communication and organizational skills. However, with mentorship and constructive feedback, these challenges become valuable learning opportunities for professional growth.

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

AspectAssociate Medical WriterMedical Writer
Required credentialsBachelor's degree, often in life sciences or related fieldBachelor's or higher degree, often with some experience
Work environmentEntry-level, training-focused, often in pharmaceutical or biotech companiesMore independent, involved in complex document creation for regulatory or scientific purposes
Employer usagePharmaceutical, biotech, medical communications agenciesPharmaceutical companies, CROs, medical communication firms

The main difference between an Associate Medical Writer and a Medical Writer lies in experience and responsibility. Associate Medical Writers are typically entry-level, focusing on learning and supporting document preparation, while Medical Writers handle more complex projects independently. Both roles require similar educational backgrounds and are common in the pharmaceutical and biotech industries.

What does an associate medical writer do?

An Associate Medical Writer is responsible for creating scientific documents, such as clinical study reports, regulatory submissions, and manuscripts for publication. They work closely with medical professionals, researchers, and regulatory teams to ensure accuracy and compliance with guidelines. Their role often involves interpreting complex scientific data and presenting it in a clear, concise manner for different audiences. Associate Medical Writers are typically early in their medical writing careers and receive guidance from more senior writers as they develop their skills.

What are the most commonly searched types of Medical Writer jobs in Delaware?

The most popular types of Medical Writer jobs in Delaware are:

What are popular job titles related to Associate Medical Writer jobs in Delaware?

For Associate Medical Writer jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Associate Medical Writer jobs in Delaware look for?

The top searched job categories for Associate Medical Writer jobs in Delaware are:

What cities in Delaware are hiring for Associate Medical Writer jobs?

Cities in Delaware with the most Associate Medical Writer job openings:

Associate Medical Writer jobs near you
Infographic showing various Associate Medical Writer job openings in Delaware as of August 2026, with employment types broken down into 75% Full Time, 16% Part Time, 2% Temporary, and 7% Contract. Highlights an 79% In-person, 8% Hybrid, and 13% Remote job distribution, with an average salary of $80,433 per year, or $38.7 per hour.

Associate Director Companion Diagnostics Lead, Translational Sciences

Incyte Corporation

Wilmington, DE • On-site

Full-time

Re-posted 13 days ago

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.
Job Summary (Primary function)
Associate Director, Companion Diagnostics Lead is a leadership role responsible for the development and implementation of clinical diagnostic plans including companion diagnostics (CDx) requirements within drug development programs. This involves active participation in CDx strategy setup and deployment, managing logistics, vendor selection and relationships, and ensuring timely CDx delivery.
Key duties include:
  • Serve as subject matter expert in CDx development process (from concept to commercialization)
  • Lead selection and management of diagnostic partners
  • Monitor assay analytical and clinical performance evaluation activities
  • Author CDx related parts across documents
  • Ensure CDx representation in cross-functional teams

  • Serve as alliance and project manager between Incyte and key diagnostic partners
  • Generate and review new project agreements as needed
  • Manage and maintain CDx budget for projects
  • Track and approve milestones for each project
  • Lead Joint project team (JPT) meetings with alliance partner

  • Supervise validation and implementation of clinical trial assay (CTA) at testing laboratory
  • Maintain alignment between diagnostics partner and testing laboratory
  • Ensure timelines are met
  • Oversee operational aspects of clinical implementation

  • Ensure compliance with regulatory and ethical guidelines
  • Develop and apply expertise in regulatory requirements for CDx across regions (US FDA, EU IVDR etc)
  • Supervise Incyte review of CDx documentation such as clinical study performance plans (CPSP), Instructions for Use etc
  • Ensure creation and review of informed consent, CPSP and country submissions/responses are timely and compliant
  • Develop and Maintain Expertise in Delivery of Companion Diagnostics
  • Maintain relationships with key stakeholders

Qualifications (Minimal acceptable level of education, work experience, and competency)
  • Minimum BS Degree in a scientific discipline with 7+ years of experience in the diagnostic and/or pharmaceutical industry (clinical studies).
  • Understanding of Good Clinical Practices (GCP) and relevant regulatory requirements. Ability to manage external research activities through CROs and collaborators.
  • Ability to balance execution of multiple tasks to accomplish program goals.
  • A high level of emotional intelligence and willing to work closely and collaboratively with other functional groups internal and external to the company.
  • Exceptional verbal and written communication skills.

Preferred Qualifications:
  • Advanced degree in a scientific discipline with extensive experience in CDx development, registration and commercialization and IVD clinical studies.
  • Extensive knowledge of assay development using Next Generation Sequencing, PCR and Immunohistochemistry.
  • Experience in CDx and/or precision medicine including IVDR.

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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