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Clinical Editor Jobs in Delaware (NOW HIRING)

Nemours-Children

Clinical Research Coordinator

Wilmington, DE · On-site

$23.50 - $31.25/hr

Provide non-technical writing, formatting, and editing support; inclusive of budget justifications ... Clinical Research Coordinator certification or eligible to sit for exam after 2 years clinical ...

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Option Care

Clinical Pharmacy Technician I

Newark, DE · On-site

Through our clinical leadership, expertise and national scale, Option Care Health is re-imagining ... editing text, changing views, inserting a table or a note, moving objects, printing outline view ...

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How much do clinical editor jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for clinical editor in Delaware is $43.31, according to ZipRecruiter salary data. Most workers in this role earn between $43.32 and $43.32 per hour, depending on experience, location, and employer.

What are some common challenges faced by clinical editors when working with medical manuscripts?

Clinical Editors often encounter challenges such as ensuring the accuracy and clarity of complex medical information, adhering to strict journal or regulatory guidelines, and meeting tight publication deadlines. Additionally, they may need to bridge communication gaps between authors, reviewers, and publishers, all while maintaining scientific integrity and consistency in terminology. Staying updated with evolving medical standards and best practices is also essential for success in this role.

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

To thrive as a Clinical Editor, you need a solid background in healthcare or life sciences, excellent writing and editing skills, and familiarity with medical terminology, often supported by a relevant degree. Familiarity with referencing management software, medical databases like PubMed, and style guides such as AMA or APA is typically required. Attention to detail, critical thinking, and effective communication are essential soft skills for ensuring accuracy and clarity in clinical content. These skills ensure that medical information is both precise and accessible, supporting high-quality healthcare communication and patient safety.

What is the difference between Clinical Editor vs Medical Writer?

AspectClinical EditorMedical Writer
Required CredentialsBachelor's degree in life sciences, editing certifications beneficialBachelor's or higher in life sciences, writing experience
Work EnvironmentPublishing companies, pharmaceutical firms, research organizationsPharmaceutical companies, healthcare agencies, freelance
Employer & Industry UsageEditing scientific content, ensuring clarity and accuracyCreating scientific documents, reports, and publications

Both roles often require a background in life sciences and involve working with scientific content. A Clinical Editor primarily focuses on reviewing and editing clinical and scientific materials for clarity and accuracy, while a Medical Writer creates original scientific documents. Understanding these differences helps professionals choose the right career path or job search focus.

What does a clinical editor do?

A clinical editor reviews and revises medical and scientific content to ensure accuracy, clarity, and consistency. They often work with research articles, clinical trial reports, and healthcare publications, using editing skills and knowledge of medical terminology to improve the quality of the material.

What are popular job titles related to Clinical Editor jobs in Delaware?

For Clinical Editor jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Clinical Editor jobs in Delaware look for?

The top searched job categories for Clinical Editor jobs in Delaware are:

What are popular job titles related to Clinical Editor jobs in DE?

For Clinical Editor jobs in DE, the most frequently searched job titles are:

Clinical Editor jobs near you
Infographic showing various Clinical Editor job openings in Delaware as of August 2026, with employment types broken down into 2% As Needed, 75% Full Time, 16% Part Time, and 7% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $90,077 per year, or $43.3 per hour.

Clinical Research Coordinator

Wilmington, DE • On-site

Nemours-Children
See more jobs at Nemours-Childrenexternal

$23.50 - $31.25/hr

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Job description

Primary Function

TheNemours Anesthesia and Surgical Outcomes Center (NASOC) Clinical Research Coordinator will support clinical research activities for the department, division, and/or center. This position will serve as a vital resource for investigators to partner and facilitate the conduct of various research studies and liaison with research administration as well as various institutional committees. The incumbent will serve as a point of contact for assigned areas and provide day-to-day support to the ongoing studies, publications, presentations, posters, and other academic work as assigned. As a result, the clinical research coordinator will help to advance research throughout the department and divisions as assigned. This position will also support projects and assumes responsibility for the day-to-day operation of program activities, including the regulatory functions, project management, administrative tasks, study conduct, chart review, study enrollment, basic data analysis, RedCap, interpretation of results and reporting of research studies and experiments. Possesses advanced knowledge of research practices.

Essential Functions
  1. Follows all aspects of Standard Operating Procedures and Good Clinical Practices in the conduct of clinical research; collects and prepares documents as required to ensure compliance with sponsor and regulatory guidelines; oversee clinical research projects within the department and divisions.
  2. Understands and can conduct clinical research studies that require but not limited to Emergent Access/Compassionate use, multi-site clinical trials, conduct Investigator Initiated studies, Research Team training manuals. Maintains scientific knowledge and understanding of peer-reviewed publications for application to current methodologies.
  3. Participates in the design and completion of study protocols; including but not limited to regulatory support and maintenance, the conduct of parental permission/assent process for assigned studies; enrolls study participants; schedules study visits with study participants in accordance with study protocols; develops strategies to assure compliance of study participants with protocol requirements.
  4. Performs clinical data gathering, measurements including medical record review when needed and monitoring of data integrity, including data completeness, accuracy, and quality. Maintains and contributes to the creation of multiple study databases, including but not limited to RedCap. Ability to submit data proactively, address queries in a timely manner, and identify and resolve concerns related to research projects.
  5. Participates in training study team members for study purposes; builds relationships with various departments to ensure protocol compliance.
  6. Assists in identifying, reporting and following-up on Serious Adverse Events and/or Unanticipated problems
  7. Assists in the maintenance of study medication accountability records; works closely with research pharmacist to coordinate study drug administration and documentation.
  8. Prepares clinical specimens for shipment to central laboratories. Ensures manual of procedures is followed and applicable documentation is sent with samples
  9. Coordinates monitoring activities with Sponsor’s representative(s). Completes Case Report Forms; responds to sponsor queries, prepares for internal and external audits by sponsor, IRB and/or the FDA/DHHS.
  10. Participates in continuous process improvement initiatives and implementation of outcomes. Advise and collaborate with Principal Investigators on strategies to enhance research activity.
  11. Provide non-technical writing, formatting, and editing support; inclusive of budget justifications, biographical sketches, institutional background descriptions, references, appendices, and other proposal documents. Assist the PI and research team prepare presentations for scientific meetings, describing the methodology and results; prepare manuscripts for publication in peer-reviewed journals; and prepare grant applications.
Requirements
  • Bachelor’s degree in medical or science related field required;
  • At least one year of Research experience required
  • Effectively uses Microsoft computer software; demonstrates ability to coordinate and establish priorities among diverse tasks; effectively communicates verbally and in writing
  • Clinical Research Coordinator certification or eligible to sit for exam after 2 years clinical research coordination experience

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