The Pharmacokinetic Scientist will assist with pharmacokinetic data analysis, scientific interpretation of study results, clinical report writing, and interactions with clients. Essential Functions
The Pharmacokinetic Scientist will assist with pharmacokinetic data analysis, scientific interpretation of study results, clinical report writing, and interactions with clients. Essential Functions
The Pharmacokinetic Scientist will assist with pharmacokinetic data analysis, scientific interpretation of study results, clinical report writing, and interactions with clients. Essential Functions
The Pharmacokinetic Scientist will assist with pharmacokinetic data analysis, scientific interpretation of study results, clinical report writing, and interactions with clients. Essential Functions
$125 - $150/hr
Other (20%): may involve clinical report drafting, test validation, process refinement, presenting ... Excellence in reading and writing medical language. * Proficiency in Microsoft Office (Excel, Word ...
$125 - $150/hr
Other (20%): may involve clinical report drafting, test validation, process refinement, presenting ... Excellence in reading and writing medical language. * Proficiency in Microsoft Office (Excel, Word ...
Other (20%) : may involve clinical report drafting, test validation, process refinement, presenting ... Excellence in reading/writing medical language. * Proficiency in Microsoft Office (Excel, Word ...
Other (20%) : may involve clinical report drafting, test validation, process refinement, presenting ... Excellence in reading/writing medical language. * Proficiency in Microsoft Office (Excel, Word ...
Clinical Writer
Irvine, CA · On-site
$42 - $44/hr
Clinical Writer Location: Irvine, CA (contract-onsite) Duration: 6 Months Pay: $42- $44/hr on W2 ... Prepare clinical study reports (CSRs) under supervisor direction. Based on the clinical study ...
Clinical Writer
Irvine, CA · On-site
$42 - $44/hr
Clinical Writer Location: Irvine, CA (contract-onsite) Duration: 6 Months Pay: $42- $44/hr on W2 ... Prepare clinical study reports (CSRs) under supervisor direction. Based on the clinical study ...
Licensed Clinician
Pittsfield, MA · On-site
$78K/yr
Additional responsibilities include treatment team facilitation, clinical report writing and coordination of student treatment plans. The Clinician works with the clinical support team to ensure all ...
Licensed Clinician
Pittsfield, MA · On-site
$78K/yr
Additional responsibilities include treatment team facilitation, clinical report writing and coordination of student treatment plans. The Clinician works with the clinical support team to ensure all ...
The Pharmacokinetic Scientist will assist with pharmacokinetic data analysis, scientific interpretation of study results, clinical report writing, and interactions with clients. Essential Functions
The Pharmacokinetic Scientist will assist with pharmacokinetic data analysis, scientific interpretation of study results, clinical report writing, and interactions with clients. Essential Functions
Clinical Writer I
Richardson, TX · On-site
Drafts protocols and reports for clinical studies on cosmetics or other claims. * Uses internal or ... Writes and reviews ICH/GCP-adherent clinical study protocols, coordinates internal and external ...
Clinical Writer I
Richardson, TX · On-site
Drafts protocols and reports for clinical studies on cosmetics or other claims. * Uses internal or ... Writes and reviews ICH/GCP-adherent clinical study protocols, coordinates internal and external ...
Clinical Writer I
Richardson, TX · On-site
Drafts protocols and reports for clinical studies on cosmetics or other claims. * Uses internal or ... Writes and reviews ICH/GCP-adherent clinical study protocols, coordinates internal and external ...
Clinical Writer I
Richardson, TX · On-site
Drafts protocols and reports for clinical studies on cosmetics or other claims. * Uses internal or ... Writes and reviews ICH/GCP-adherent clinical study protocols, coordinates internal and external ...
$110K - $114K/yr
... writing, clinical report drafting, or sequencing result analysis Thorough and ongoing knowledge of current theories and principles of human genetics Ability to understand and evaluate genetic data ...
$110K - $114K/yr
... writing, clinical report drafting, or sequencing result analysis Thorough and ongoing knowledge of current theories and principles of human genetics Ability to understand and evaluate genetic data ...
Clinical Genomic Scientist II (genome analyst): REMOTE, USA
$110K - $114K/yr
... writing, clinical report drafting, or sequencing result analysis • Thorough and ongoing knowledge of current theories and principles of human genetics • Ability to understand and evaluate genetic ...
Clinical Genomic Scientist II (genome analyst): REMOTE, USA
$110K - $114K/yr
... writing, clinical report drafting, or sequencing result analysis • Thorough and ongoing knowledge of current theories and principles of human genetics • Ability to understand and evaluate genetic ...
$110K - $114K/yr
... writing, clinical report drafting, or sequencing result analysis Thorough and ongoing knowledge of current theories and principles of human genetics Ability to understand and evaluate genetic data ...
$110K - $114K/yr
... writing, clinical report drafting, or sequencing result analysis Thorough and ongoing knowledge of current theories and principles of human genetics Ability to understand and evaluate genetic data ...
Clinical Genomic Scientist II (genome analyst): REMOTE, USA
$110K - $114K/yr
... writing, clinical report drafting, or sequencing result analysis • Thorough and ongoing knowledge of current theories and principles of human genetics • Ability to understand and evaluate genetic ...
Clinical Genomic Scientist II (genome analyst): REMOTE, USA
$110K - $114K/yr
... writing, clinical report drafting, or sequencing result analysis • Thorough and ongoing knowledge of current theories and principles of human genetics • Ability to understand and evaluate genetic ...
... report-writing work on a 1099 basis ... This opportunity is ideal for a psychiatrist with strong clinical judgment, a professional ...
... report-writing work on a 1099 basis ... This opportunity is ideal for a psychiatrist with strong clinical judgment, a professional ...
... report-writing work on a 1099 basis ... This opportunity is ideal for a psychiatrist with strong clinical judgment, a professional ...
... report-writing work on a 1099 basis ... This opportunity is ideal for a psychiatrist with strong clinical judgment, a professional ...
... report-writing work on a 1099 basis ... This opportunity is ideal for a psychiatrist with strong clinical judgment, a professional ...
... report-writing work on a 1099 basis ... This opportunity is ideal for a psychiatrist with strong clinical judgment, a professional ...
Senior Medical Writer
Boulder, CO · On-site
Works with clinical, data management and biostatistics staff to develop report formats and write final drafts of clinical study reports. Participates in review of clinical data interpretation for ...
Senior Medical Writer
Boulder, CO · On-site
Works with clinical, data management and biostatistics staff to develop report formats and write final drafts of clinical study reports. Participates in review of clinical data interpretation for ...
$100 - $125/hr
... writing, clinical report drafting, or sequencing result analysis * Thorough and ongoing knowledge of current theories and principles of human genetics * Ability to understand and evaluate genetic ...
$100 - $125/hr
... writing, clinical report drafting, or sequencing result analysis * Thorough and ongoing knowledge of current theories and principles of human genetics * Ability to understand and evaluate genetic ...
Prepares clinical reports, summary documents, investigator's brochures, package inserts, protocols ... Excellent written/oral communication skills. Good interpersonal skills; able to establish rapport ...
Prepares clinical reports, summary documents, investigator's brochures, package inserts, protocols ... Excellent written/oral communication skills. Good interpersonal skills; able to establish rapport ...
Prepares clinical reports, summary documents, investigator's brochures, package inserts, protocols ... Excellent written/oral communication skills. Good interpersonal skills; able to establish rapport ...
Prepares clinical reports, summary documents, investigator's brochures, package inserts, protocols ... Excellent written/oral communication skills. Good interpersonal skills; able to establish rapport ...
Clinical Report Writer information
See salary details
$42K - $50.5K
16% of jobs
$54.5K is the 25th percentile. Wages below this are outliers.
$50.5K - $59.1K
20% of jobs
$59.1K - $67.6K
8% of jobs
The median wage is $71.9K / yr.
$67.6K - $76.2K
12% of jobs
$76.2K - $84.7K
15% of jobs
$84.7K - $93.3K
3% of jobs
$95.1K is the 75th percentile. Wages above this are outliers.
$93.3K - $101.8K
6% of jobs
$101.8K - $110.4K
17% of jobs
$110.4K - $118.9K
0% of jobs
$118.9K - $127.5K
0% of jobs
$127.5K - $136K
3% of jobs
$42K
$78.9K
$136K
How much do clinical report writer jobs pay per year?
As of Sep 8, 2026, the average yearly pay for clinical report writer in the United States is $78,865.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,500.00 and $102,000.00 per year, depending on experience, location, and employer.
What is the difference between Clinical Report Writer vs Medical Writer?
| Aspect | Clinical Report Writer | Medical Writer |
|---|---|---|
| Credentials | Often requires a background in healthcare, life sciences, or related fields; certifications like RAC or CCR may be preferred | Typically holds degrees in life sciences, healthcare, or communications; certifications like AMWA or EMWA are common |
| Work Environment | Works in clinical research settings, pharmaceutical companies, or healthcare organizations | Works in publishing, pharmaceutical, biotech, or healthcare communication firms |
| Industry Usage | Used primarily in clinical trial documentation and regulatory submissions | Used for scientific publications, marketing materials, and regulatory documents |
While both roles involve scientific writing, Clinical Report Writers focus on clinical trial documentation and regulatory reports, whereas Medical Writers produce a broader range of medical content including publications and marketing materials. The roles often overlap but serve different primary purposes within the healthcare and pharmaceutical industries.
What does a clinical report writer do?
A clinical report writer creates detailed documents that summarize clinical trial data, research findings, and medical information for regulatory submissions, publications, or internal use. They often use specialized software and must ensure accuracy, clarity, and compliance with industry standards. Strong writing skills and knowledge of medical terminology are essential for this role.
What cities are hiring for Clinical Report Writer jobs?
Cities with the most Clinical Report Writer job openings:
What states have the most Clinical Report Writer jobs?
States with the most job openings for Clinical Report Writer jobs include:
What are popular job titles related to Clinical Report Writer jobs?
For Clinical Report Writer jobs, the most frequently searched job titles are:
Celerion rating
7.0
Based on 13 frontline employees who took The Breakroom Quiz
64th of 75 rated research
Job description
We are looking for a full-time Pharmacokinetic Scientist to join our Clinical Pharmacology team. This role may be based at either our Lincoln, NE, or Montreal, Canada facilities. Remote working relationships may be considered based upon experience. The Pharmacokinetic Scientist will assist with pharmacokinetic data analysis, scientific interpretation of study results, clinical report writing, and interactions with clients.
Essential Functions
- Data analysis and interpretation
- Perform PK analyses independently
- Assist with PD analyses
- Interpret PK and statistical results and findings independently
- Perform QC reviews as assigned
- Write and review reports as assigned
- Prepare PK data/report files for electronic filing of projects for submission to regulatory agencies
- Maintain and file all supportive documentation pertaining to the study and ensure proper archiving of projects
- Other responsibilities
- Interact with clients alongside or under direction of a senior scientist, as needed
- Prepare internal presentations
Requirements
- Master's or PhD degree in a biology-focused sciences related field with 2+ years of related experience required
- Competence in performing noncompartmental pharmacokinetic analysis with software applications such as Phoenix WinNonlin
- Familiarity with processes and applications related to non-linear mixed-effect modeling and/or physiologically-based pharmacokinetic modeling is an asset
- Excellent oral and written skills (English language) required
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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About Celerion
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Lincoln, NE, US
Year founded
2010