We are now recruiting an Associate Director, R&I Clinical Regulatory Writing (CReW). As part of a clinical delivery or submission team, the Associate Director provides strategic communications
We are now recruiting an Associate Director, R&I Clinical Regulatory Writing (CReW). As part of a clinical delivery or submission team, the Associate Director provides strategic communications
Employment Type: Full timeShift: Description: Why Mount Carmel? With five hospitals, over 60 free-standing outpatient clinics, a college of nursing, a Medicare Advantage plan, and extensive outreach
Employment Type: Full timeShift: Description: Why Mount Carmel? With five hospitals, over 60 free-standing outpatient clinics, a college of nursing, a Medicare Advantage plan, and extensive outreach
Employment Type: Full timeShift: Description: Why Mount Carmel? With five hospitals, over 60 free-standing outpatient clinics, a college of nursing, a Medicare Advantage plan, and extensive outreach
Employment Type: Full timeShift: Description: Why Mount Carmel? With five hospitals, over 60 free-standing outpatient clinics, a college of nursing, a Medicare Advantage plan, and extensive outreach
We are now recruiting anAssociateDirector,R&IClinical Regulatory Writing (CReW). As part of a clinical delivery or submission team,the Associate Directorprovidesstrategic communications leadership to
We are now recruiting anAssociateDirector,R&IClinical Regulatory Writing (CReW). As part of a clinical delivery or submission team,the Associate Directorprovidesstrategic communications leadership to
Employment Type: Full time Shift: Description: Why Mount Carmel? With five hospitals, over 60 free-standing outpatient clinics, a college of nursing, a Medicare Advantage plan, and extensive outreach
Employment Type: Full time Shift: Description: Why Mount Carmel? With five hospitals, over 60 free-standing outpatient clinics, a college of nursing, a Medicare Advantage plan, and extensive outreach
Associate Director, R&I Clinical Regulatory Writing (CReW)
Gaithersburg, MD · On-site
$136K - $205K/yr
We are now recruiting anAssociateDirector,R&IClinical Regulatory Writing (CReW). As part of a clinical delivery or submission team,the Associate Directorprovidesstrategic communications leadership to
Associate Director, R&I Clinical Regulatory Writing (CReW)
Gaithersburg, MD · On-site
$136K - $205K/yr
We are now recruiting anAssociateDirector,R&IClinical Regulatory Writing (CReW). As part of a clinical delivery or submission team,the Associate Directorprovidesstrategic communications leadership to
Principal Medical Writer
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Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its
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Assistant Director Clinical Regulatory OperationsSkip to main content#Assistant Director Clinical Regulatory Operations page is loaded## Assistant Director Clinical Regulatory
Assistant Director Clinical Regulatory OperationsSkip to main content#Assistant Director Clinical Regulatory Operations page is loaded## Assistant Director Clinical Regulatory
$130K - $140K/yr
Senior Staff Clinical Regulatory Scientist Location: Leesburg, VA, Allendale, NJ or Remote | 20% Travel Required Company: VB Spine Looking for a career where your work truly matters? At VB Spine,
New
$130K - $140K/yr
Senior Staff Clinical Regulatory Scientist Location: Leesburg, VA, Allendale, NJ or Remote | 20% Travel Required Company: VB Spine Looking for a career where your work truly matters? At VB Spine,
New
Sr. Staff Clinical Regulatory Scientist
Allendale, NJ · On-site +1
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Senior Staff Clinical Regulatory Scientist Location: Leesburg, VA, Allendale, NJ or Remote | 20% Travel Required Company: VB Spine Looking for a career where your work truly matters? At VB Spine,
Sr. Staff Clinical Regulatory Scientist
Allendale, NJ · On-site +1
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Senior Staff Clinical Regulatory Scientist Location: Leesburg, VA, Allendale, NJ or Remote | 20% Travel Required Company: VB Spine Looking for a career where your work truly matters? At VB Spine,
Assistant Director Clinical Regulatory Operations Hybrid role (3 days/week in office) at our Burlington, Renton, Spokane, Vancouver, Portland, Medford, Salt Lake City, Boise, Lewiston, Fargo offices.
Assistant Director Clinical Regulatory Operations Hybrid role (3 days/week in office) at our Burlington, Renton, Spokane, Vancouver, Portland, Medford, Salt Lake City, Boise, Lewiston, Fargo offices.
Assistant Director Clinical Regulatory Operations Hybrid role (3 days/week in office) at our Burlington, Renton, Spokane, Vancouver, Portland, Medford, Salt Lake City, Boise, Lewiston, Fargo offices.
Assistant Director Clinical Regulatory Operations Hybrid role (3 days/week in office) at our Burlington, Renton, Spokane, Vancouver, Portland, Medford, Salt Lake City, Boise, Lewiston, Fargo offices.
Assistant Director Clinical Regulatory Operations Hybrid role (3 days/week in office) at our Burlington, Renton, Spokane, Vancouver, Portland, Medford, Salt Lake City, Boise, Lewiston, Fargo offices.
Assistant Director Clinical Regulatory Operations Hybrid role (3 days/week in office) at our Burlington, Renton, Spokane, Vancouver, Portland, Medford, Salt Lake City, Boise, Lewiston, Fargo offices.
Medical Writer / Clinical Document Author
Honolulu, HI · Remote
$50 - $80/hr
Role Title: Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project
Medical Writer / Clinical Document Author
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Medical Writer / Clinical Document Author
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Role Title: Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project
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Tyler, TX · Remote
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Role Title: Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project
Clinical Regulatory Writer information
See salary details
$25 - $30.31
10% of jobs
$30.31 - $35.62
9% of jobs
$39.07 is the 25th percentile. Wages below this are outliers.
$35.62 - $40.93
11% of jobs
$40.93 - $46.24
2% of jobs
$46.24 - $51.55
1% of jobs
The median wage is $55.31 / hr.
$51.55 - $56.86
26% of jobs
$56.86 - $62.17
15% of jobs
$63.28 is the 75th percentile. Wages above this are outliers.
$62.17 - $67.48
13% of jobs
$67.48 - $72.79
10% of jobs
$72.79 - $78.10
4% of jobs
$78.10 - $83.41
1% of jobs
$25
$54
$83
How much do clinical regulatory writer jobs pay per hour?
As of Sep 13, 2026, the average hourly pay for clinical regulatory writer in the United States is $54.35, according to ZipRecruiter salary data. Most workers in this role earn between $39.90 and $64.18 per hour, depending on experience, location, and employer.
What cities are hiring for Clinical Regulatory Writer jobs?
Cities with the most Clinical Regulatory Writer job openings:
What states have the most Clinical Regulatory Writer jobs?
States with the most job openings for Clinical Regulatory Writer jobs include:
What are popular job titles related to Clinical Regulatory Writer jobs?
For Clinical Regulatory Writer jobs, the most frequently searched job titles are:
Associate Director, R&I Clinical Regulatory Writing (CReW)
Gaithersburg, MD • On-site
AstraZeneca
• Pharmaceutical Product Wholesalers • 10K+ employees10,000+ employees
Full-time
Medical, Dental, Vision, Retirement, PTO
Re-posted 8 days ago
AstraZeneca rating
8.4
Based on 45 frontline employees who took The Breakroom Quiz
Job description
We are now recruiting an Associate Director, R&I Clinical Regulatory Writing (CReW). As part of a clinical delivery or submission team, the Associate Director provides strategic communications leadership to projects, establishes communication standards and best practice, and continuously advocates for quality and efficiency. The Associate Director also authors strategic clinical-regulatory documents and provides critical review to achieve high-quality standards, utilizing best practices for document and accelerated submission delivery.
What You will Do
The Associate Director, CReW, is expected to:
Minimum Qualifications:
Desirable Qualifications:
Why AstraZeneca?
At AstraZeneca we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There's no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We're on an exciting journey to pioneer the future of healthcare.
So, what's next?
Are you already imagining yourself joining our team? Good, because we can't wait to hear from you!
The annual base pay (or hourly rate of compensation) for this position ranges from $136,784.80 - $205,177.20 USD. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
Date Posted
09-Sep-2026
Closing Date
30-Sep-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
What You will Do
The Associate Director, CReW, is expected to:
- Independently manage clinical regulatory writing activities across a portfolio of work.
- Author clinical-regulatory documents within a program by ensuring that relevant regulatory, technical, and quality standards are achieved, and that relevant processes and best practice are applied.
- Drive the development of the clinical Submission Communication Strategy.
- Lead internal/external authoring teams and provide strong partnership with vendor medical writers to ensure delivery to time and quality.
- Drive the clinical interpretation of complex data and information and condense it into clear, concise and accurate messages that address information requirements.
- Be a strategic thinker and demonstrate strategic review capabilities.
- Proactively collaborative with other functions at the program level.
- Support the development of others in Clinical Regulatory Writing.
- Drive continuous improvement and operational excellence from a communications leadership perspective, including representing the Clinical Regulatory Writing function on drug and non-drug projects, as required.
Minimum Qualifications:
- A Bachelor's degree
- At least 5 years of experience in the medical/regulatory writing field gained in a pharmaceutical/biotech industry or Contract Research Organization environment.
- Experience leading submission authoring and authoring submission level documents.
- Understanding of the drug development process from development through life-cycle management.
- Experience in working within, and contributing to, large, diverse, matrix teams.
- Excellent verbal and written communication skills in English.
- In depth knowledge of the technical and regulatory requirements related to the role.
- Flexibility in adapting to changing circumstances and latest information.
Desirable Qualifications:
- Advanced degree in a scientific discipline (Ph.D.).
Why AstraZeneca?
At AstraZeneca we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There's no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We're on an exciting journey to pioneer the future of healthcare.
So, what's next?
Are you already imagining yourself joining our team? Good, because we can't wait to hear from you!
The annual base pay (or hourly rate of compensation) for this position ranges from $136,784.80 - $205,177.20 USD. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
Date Posted
09-Sep-2026
Closing Date
30-Sep-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
What AstraZeneca employees say
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About AstraZeneca
Sourced by ZipRecruiter
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.
Industry
Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing
Company size
10,000+ Employees
Headquarters location
Cambridge, Cambridgeshire, GB