Highly proficient with styles of writing for various regulatory documents * Expert proficiency with client templates & style guides * Interact directly and independently with client to coordinate all ...
Quick apply
Highly proficient with styles of writing for various regulatory documents * Expert proficiency with client templates & style guides * Interact directly and independently with client to coordinate all ...
Regulatory Manager
Yuma, AZ · On-site
... write and orally communicate technical issues. · Successful experience managing the regulatory issues for active ingredients. · Detail oriented with proven leadership skills and strong ...
Regulatory Manager
Yuma, AZ · On-site
... write and orally communicate technical issues. · Successful experience managing the regulatory issues for active ingredients. · Detail oriented with proven leadership skills and strong ...
Description The Regulatory Administrator II is a fully onsite, customer-facing role responsible for ... Strong written and verbal communication skills. * Ability to manage multiple tasks, priorities, and ...
Description The Regulatory Administrator II is a fully onsite, customer-facing role responsible for ... Strong written and verbal communication skills. * Ability to manage multiple tasks, priorities, and ...
Regulatory Specialist
Phoenix, AZ · On-site
Regulatory Specialist We are Lennar Lennar is one of the nation's leading homebuilders, dedicated ... Effective verbal and written communication skills * Strong attention to detail and accuracy
Regulatory Specialist
Phoenix, AZ · On-site
Regulatory Specialist We are Lennar Lennar is one of the nation's leading homebuilders, dedicated ... Effective verbal and written communication skills * Strong attention to detail and accuracy
Regulatory Administrator
Mesa, AZ · On-site
Description The Regulatory Administrator II is a fully onsite, customer-facing role responsible for ... Strong written and verbal communication skills. * Ability to manage multiple tasks, priorities, and ...
Regulatory Administrator
Mesa, AZ · On-site
Description The Regulatory Administrator II is a fully onsite, customer-facing role responsible for ... Strong written and verbal communication skills. * Ability to manage multiple tasks, priorities, and ...
Regulatory Specialist
Phoenix, AZ · On-site +1
Regulatory Specialist We are Lennar Lennar is one of the nation's leading homebuilders, dedicated ... Effective verbal and written communication skills * Strong attention to detail and accuracy
Regulatory Specialist
Phoenix, AZ · On-site +1
Regulatory Specialist We are Lennar Lennar is one of the nation's leading homebuilders, dedicated ... Effective verbal and written communication skills * Strong attention to detail and accuracy
Regulatory Administrator
Mesa, AZ · On-site
The Regulatory Administrator is responsible for providing regulatory, immigration, and student ... Strong written and verbal communication skills. * Strong organizational, prioritization, and time ...
Regulatory Administrator
Mesa, AZ · On-site
The Regulatory Administrator is responsible for providing regulatory, immigration, and student ... Strong written and verbal communication skills. * Strong organizational, prioritization, and time ...
Regulatory Administrator
Mesa, AZ · On-site
The Regulatory Administrator is responsible for providing regulatory, immigration, and student ... Strong written and verbal communication skills. * Strong organizational, prioritization, and time ...
Regulatory Administrator
Mesa, AZ · On-site
The Regulatory Administrator is responsible for providing regulatory, immigration, and student ... Strong written and verbal communication skills. * Strong organizational, prioritization, and time ...
Regulatory & Clinical Specialist
Phoenix, AZ · Remote
$85K - $95K/yr
Experience writing Clinical Evaluation Plans and Reports (CEP, CER, respectively) to support EU MDD and MDR requirements. * Expertise in conducting focused literature searches on PubMed, Embase ...
Regulatory & Clinical Specialist
Phoenix, AZ · Remote
$85K - $95K/yr
Experience writing Clinical Evaluation Plans and Reports (CEP, CER, respectively) to support EU MDD and MDR requirements. * Expertise in conducting focused literature searches on PubMed, Embase ...
Strong written and verbal communication skills, with the ability to collaborate effectively across ... Industry Regulatory Authority (FINRA) and the National Futures Association (NFA). The major ...
Strong written and verbal communication skills, with the ability to collaborate effectively across ... Industry Regulatory Authority (FINRA) and the National Futures Association (NFA). The major ...
Strong written and verbal communication skills, with the ability to collaborate effectively across ... Industry Regulatory Authority (FINRA) and the National Futures Association (NFA). The major ...
Strong written and verbal communication skills, with the ability to collaborate effectively across ... Industry Regulatory Authority (FINRA) and the National Futures Association (NFA). The major ...
Regulatory Affairs Leader
Flagstaff, AZ · On-site
Willingness to share experience and coach Regulatory Associates in order to successfully execute on regulatory assessments, submission strategy, and submission writing * Experience with regulatory ...
Regulatory Affairs Leader
Flagstaff, AZ · On-site
Willingness to share experience and coach Regulatory Associates in order to successfully execute on regulatory assessments, submission strategy, and submission writing * Experience with regulatory ...
Provide accurate, complete, and timely written regulatory communications throughout the regulatory exam and continuous monitoring lifecycle * Support system of record enhancements. Maintain exam ...
Provide accurate, complete, and timely written regulatory communications throughout the regulatory exam and continuous monitoring lifecycle * Support system of record enhancements. Maintain exam ...
Provide accurate, complete, and timely written regulatory communications throughout the regulatory exam and continuous monitoring lifecycle * Support system of record enhancements. Maintain exam ...
Provide accurate, complete, and timely written regulatory communications throughout the regulatory exam and continuous monitoring lifecycle * Support system of record enhancements. Maintain exam ...
Regulatory Affairs Expert - Remote
Phoenix, AZ · Remote
$50 - $80/hr
Prepare structured, guideline-based written feedback. Required Qualifications * 5+ years of Regulatory Affairs experience in the pharmaceutical, biotech, or CRO industry. * Experience with clinical ...
Quick apply
Regulatory Affairs Expert - Remote
Phoenix, AZ · Remote
$50 - $80/hr
Prepare structured, guideline-based written feedback. Required Qualifications * 5+ years of Regulatory Affairs experience in the pharmaceutical, biotech, or CRO industry. * Experience with clinical ...
Regulatory Science, Biomedical Engineering, Biology, Chemistry, English (with a technical writing emphasis), Legal Studies, Law, Nursing, Physician Assistance, Pharmaceutical Science, Pharmacy OR ...
Regulatory Science, Biomedical Engineering, Biology, Chemistry, English (with a technical writing emphasis), Legal Studies, Law, Nursing, Physician Assistance, Pharmaceutical Science, Pharmacy OR ...
Regulatory and Compliance Specialist
Phoenix, AZ · On-site
$24.96 - $36.82/hr
... Pharmacy Regulatory Compliance Specialist is responsible for assisting in the assessment and ... Requires the ability to read, write, and speak effectively in English.
Regulatory and Compliance Specialist
Phoenix, AZ · On-site
$24.96 - $36.82/hr
... Pharmacy Regulatory Compliance Specialist is responsible for assisting in the assessment and ... Requires the ability to read, write, and speak effectively in English.
Regulatory Framework & Governance, Regulatory Change Oversight, Regulatory Risk Management ... Excellent communication skills (both written and oral) to interact and manage expectations with ...
Regulatory Framework & Governance, Regulatory Change Oversight, Regulatory Risk Management ... Excellent communication skills (both written and oral) to interact and manage expectations with ...
Regulatory Framework & Governance, Regulatory Change Oversight, Regulatory Risk Management ... Excellent communication skills (both written and oral) to interact and manage expectations with ...
Regulatory Framework & Governance, Regulatory Change Oversight, Regulatory Risk Management ... Excellent communication skills (both written and oral) to interact and manage expectations with ...
Regulatory Framework & Governance, Regulatory Change Oversight, Regulatory Risk Management ... Excellent communication skills (both written and oral) to interact and manage expectations with ...
Regulatory Framework & Governance, Regulatory Change Oversight, Regulatory Risk Management ... Excellent communication skills (both written and oral) to interact and manage expectations with ...
Regulatory Writing information
See Arizona salary details
$17.75 is the 25th percentile. Wages below this are outliers.
$14.56 - $25.58
86% of jobs
$25.58 - $36.60
5% of jobs
$36.60 - $47.61
0% of jobs
$47.61 - $58.63
5% of jobs
$58.63 - $69.65
1% of jobs
$69.65 - $80.66
2% of jobs
$80.66 - $91.68
0% of jobs
$91.68 - $102.70
0% of jobs
$102.70 - $113.72
0% of jobs
$113.72 - $124.73
0% of jobs
$124.73 - $135.75
0% of jobs
$14
$32
$135
How much do regulatory writing jobs pay per hour?
As of Aug 29, 2026, the average hourly pay for regulatory writing in Arizona is $32.24, according to ZipRecruiter salary data. Most workers in this role earn between $20.82 and $24.42 per hour, depending on experience, location, and employer.
What is regulatory writing?
A Regulatory Writing job involves creating and reviewing documents required for regulatory submissions in industries like pharmaceuticals, biotechnology, and medical devices. Regulatory writers ensure that documents comply with guidelines from regulatory agencies such as the FDA or EMA. Their work includes clinical study reports, investigator brochures, and regulatory submission dossiers. Strong writing skills, scientific knowledge, and attention to detail are essential for this role.
What are the key skills and qualifications needed to thrive in regulatory writing?
To thrive in Regulatory Writing, you need expertise in scientific or medical writing, an understanding of regulatory guidelines (such as FDA, EMA, or ICH), and typically a background in life sciences or related fields. Competence with document management systems, referencing tools like EndNote, and familiarity with submission platforms are often required. Strong organizational skills, attention to detail, and the ability to collaborate across multidisciplinary teams are key soft skills. These skills ensure the creation of accurate, compliant, and clear regulatory documents critical for drug and device approval processes.
What are some common challenges faced by regulatory writers in the industry?
Regulatory Writers often face tight deadlines and the need to manage complex, highly detailed documents that must comply with evolving regulatory requirements. They regularly coordinate input from diverse teams such as clinical, safety, and regulatory affairs, which can pose communication and alignment challenges. Staying current with changing international regulations and ensuring absolute accuracy in submissions are other common demands. However, these challenges also make the work engaging and offer opportunities to continuously learn and develop expertise in both scientific communication and regulatory affairs.
How much does a regulatory writing make?
Regulatory writers typically earn between $70,000 and $120,000 annually, depending on experience, location, and industry sector. Senior roles or those with specialized knowledge in areas like pharmaceuticals or biotech can command higher salaries, often supplemented by benefits and bonuses.
What does a regulatory writing do?
A regulatory writer creates and prepares documentation required for the approval of medical, pharmaceutical, or biotech products by regulatory agencies. They ensure that submissions such as clinical trial reports, safety updates, and product dossiers comply with industry standards and regulations, often using specialized tools and adhering to strict deadlines.
What is an example of regulatory writing?
Regulatory writing involves creating documents such as clinical study reports, regulatory submission dossiers, or standard operating procedures that comply with industry standards and regulatory agency requirements. These documents are essential for obtaining approvals from agencies like the FDA or EMA and require precise, clear, and well-organized language. Regulatory writers often use specialized tools and adhere to strict formatting guidelines to ensure accuracy and consistency.
What are popular job titles related to Regulatory Writing jobs in Arizona?
For Regulatory Writing jobs in Arizona, the most frequently searched job titles are:
What job categories do people searching Regulatory Writing jobs in Arizona look for?
The top searched job categories for Regulatory Writing jobs in Arizona are:
What cities in Arizona are hiring for Regulatory Writing jobs?
Cities in Arizona with the most Regulatory Writing job openings:
Senior Medical Writer (Remote)
Phoenix, AZ • On-site
MMS •
Pharmaceutical and Medicine Manufacturing • 1 - 10 employees1 - 10 employees
Full-time
Re-posted 21 days ago
Job description
About MMS
MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating.
Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.
MMS recognizes that a talented staff is what drives our business forward. Identifying and attracting top talent and continual training to strengthen core skills are essential to its core mission. At MMS, enthusiasm, collaboration, and teamwork are fostered, knowing that a global and diverse talent pool makes the company stronger. For more information, visit www.mmsholdings.com or follow MMS on LinkedIn.
Responsibilities
MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating.
Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.
MMS recognizes that a talented staff is what drives our business forward. Identifying and attracting top talent and continual training to strengthen core skills are essential to its core mission. At MMS, enthusiasm, collaboration, and teamwork are fostered, knowing that a global and diverse talent pool makes the company stronger. For more information, visit www.mmsholdings.com or follow MMS on LinkedIn.
Responsibilities
- Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias
- Write and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals
- Complete writing assignments in a timely manner
- Maintain timelines and workflow of writing assignments
- Practice good internal and external customer service
- Highly proficient with styles of writing for various regulatory documents
- Expert proficiency with client templates & style guides
- Interact directly and independently with client to coordinate all facets of projects; competent communicator skills for projects
- Contribute substantially to, or manages, production of interpretive guides
- Take ownership of a given assignment, proactively consulting other project team members and other department representatives for information or guidance as necessary
- Mentor medical writers and other members of the project team who are involved in the writing process
- At least 3 years of previous experience in the pharmaceutical industry
- Must have at least 3-5 years of industry regulatory writing and clinical medical writing experience
- The ideal candidate would hold a Bachelors, Masters, or Ph.D. in scientific, medical, clinical discipline
- Substantial clinical study protocol experience, as lead author, required
- Experience leading and managing teams while authoring regulatory documents with aggressive timelines
- Experience in regulatory submissions (clinical study reports) presented to regulatory authorities a plus
- Understanding of clinical data
- Exceptional writing skills are a must
- Excellent organizational skills and the ability to multi-task are essential prerequisites
- Candidate must be an expert in MS Word, Excel, PowerPoint, and related word processing tools
- Experience being a project lead, or managing a project team
- Strong understanding of federal regulations, Good Clinical Practices, and ICH guidelines a plus
- Not required, but experience with orphan drug designations and PSP/PIPs a plus
Powered by JazzHR
DItLGbfwtI
About M. M. S.
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
1 - 10 Employees
Headquarters location
Los Angeles, CA, US
Year founded
1980