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Associate Medical Writer Jobs in Kansas (NOW HIRING)

We're looking for an Associate Creative Director, Writer who is equal parts thinker, storyteller ... Experience with health systems, pharmaceutical brands, insurance or medical and legal review is a ...

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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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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Associate Medical Writer information

See Kansas salary details

$12

$34

$51

How much do associate medical writer jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for associate medical writer in Kansas is $34.46, according to ZipRecruiter salary data. Most workers in this role earn between $23.37 and $43.51 per hour, depending on experience, location, and employer.

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

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

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

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

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

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

Infographic showing various Associate Medical Writer job openings in Kansas as of August 2026, with employment types broken down into 62% Full Time, 27% Part Time, and 11% Contract. Highlights an 89% In-person, and 11% Hybrid job distribution, with an average salary of $71,672 per year, or $34.5 per hour.

Senior Pharmacokineticist

Olathe, KS • On-site

Other

Posted 8 days ago


Job description

JOB TITLE: Senior PharmacokineticistREPORTS TO: Associate Director, PharmacokineticsDIRECT REPORTS: Not ApplicablePOSITION SUMMARY: The Senior Pharmacokineticist serves as the lead or support for clinical Pharmacokinetic (PK) and Pharmacodynamic (PD) (hereafter referred to as “PK”) planning, analysis, and interpretation in accordance with ICH guidelines, applicable regulatory requirements, Good Clinical Practices (GCPs) and standard operating procedures (SOPs).KEY RESPONSIBILITIES:Participate in the protocol development, including study design, endpoints selection, sample size determination, and writing/reviewing the PK analysis methods sectionsSupport Case Report Form (CRF) design and review relevant data management documentsDevelop PK portion of Statistical Analysis Plan (SAP) or PK Analysis Plan(PKAP) along with relevant Tables, Listings, Figures (TLF) shellsAnalyze, interpret, summarize, and present PK data to sponsor and/or medical writer for use in Clinical Study Report (CSR) or other summary reportsConduct Quality Control (QC) review of PK analyses, text, and outputs (e.g., PK TLFs)Assists in the development of SOPs and guidelines for the PK departmentREQUIRED QUALIFICATIONS:PharmD or PhD in pharmacokinetics or related field with 3+ years clinical research experience in pharmaceutical/biotech industry (or MS with commensurate experience)Competence in performing noncompartmental analysis, including experience with software applications (e.g., Phoenix WinNonlin or R)Knowledge of PK/PD principles with relevant experience in multiple therapeutic areasUnderstanding of statistical methodologies used in clinical trials and interpretation of resultsKnowledge of FDA/ICH regulations/guidelinesExcellent verbal and written communication skills, and interpersonal skillsPREFERRED QUALIFICATIONS:Experience with additional software for the generation of PK outputs (e.g., SAS, R)Additional knowledge and/or experience in the application of routine PK compartmental modeling software systems and/or physiologically-based PK modeling #J-18808-Ljbffr