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How much do fda ctp jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for fda ctp in the United States is $51.75, according to ZipRecruiter salary data. Most workers in this role earn between $43.99 and $56.73 per hour, depending on experience, location, and employer.

What is the FDA Center for Tobacco Products (CTP)?

The FDA Center for Tobacco Products (CTP) is a division within the U.S. Food and Drug Administration responsible for regulating the manufacture, marketing, and distribution of tobacco products. Its main goal is to protect public health by ensuring that tobacco products are marketed responsibly, including overseeing product review, compliance, and enforcement. The CTP works to reduce the harm caused by tobacco use, prevent youth access, and provide accurate information to the public about tobacco products.

What are the key skills and qualifications needed to thrive as an FDA Center for Tobacco Products (CTP) professional, and why are they important?

To thrive as an FDA CTP professional, you need a background in public health, regulatory science, or a related field, often supported by relevant degrees and experience with regulatory policy. Familiarity with FDA regulatory systems, scientific data analysis tools, and compliance documentation is typically required. Strong analytical thinking, attention to detail, and effective communication are crucial soft skills for interpreting regulations and collaborating across teams. These competencies ensure regulatory compliance, effective public health protection, and successful execution of the CTP’s mission.

What is the difference between Fda Ctp vs Clinical Research Coordinator?

AspectFda CtpClinical Research Coordinator
Required CredentialsRegulatory knowledge, FDA compliance certificationsResearch ethics, clinical trial protocols, often requires a bachelor's degree
Work EnvironmentRegulatory agencies, pharmaceutical companies, biotech firmsHospitals, research sites, clinical trial centers
Industry UsageRegulatory compliance, drug approval processesManaging clinical trials, patient coordination

While both roles involve clinical and regulatory aspects, the Fda Ctp focuses on regulatory compliance and FDA processes, whereas the Clinical Research Coordinator manages day-to-day trial operations and patient interactions. Understanding these differences helps professionals choose the right career path or job focus within the clinical research industry.

What types of cross-functional teams might an FDA CTP professional collaborate with, and how does this collaboration shape daily responsibilities?

An FDA Center for Tobacco Products (CTP) professional frequently collaborates with cross-functional teams that include scientists, policy analysts, legal experts, and communications specialists. This collaboration is essential for developing and reviewing regulatory policies, evaluating scientific data on tobacco products, and ensuring compliance with federal regulations. Daily responsibilities often involve joint meetings, coordinated project management, and shared decision-making to address complex regulatory challenges. Working closely with diverse professionals enhances both the quality and efficiency of regulatory processes, while also providing valuable opportunities for skill development and career growth.
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Fda Ctp jobs near you
Infographic showing various Fda Ctp job openings in the United States as of June 2026, with employment types broken down into 79% Full Time, 14% Part Time, and 7% Contract. Highlights an 93% In-person, and 7% Remote job distribution, with an average salary of $107,647 per year, or $51.8 per hour.
Sr Manager Regulatory Submissions

Sr Manager Regulatory Submissions

Philip Morris International

Washington, DC • On-site

$176K - $220K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 9 days ago

Job description

Be a part of a revolutionary change!
At PMI, we've chosen to do something incredible. We're totally transforming our business and building our future on one clear purpose - to deliver a smoke-free future. With huge change, comes huge opportunity. So, wherever you join us, you'll enjoy the freedom to dream up and deliver better, brighter solutions and the space to move your career forward in endlessly different directions.
Our success depends on people who are committed to our purpose and have an appetite for progress.
The role entails leading the planning, authorship, and editorial quality of high-stakes regulatory documents to support U.S. tobacco/nicotine product submissions and lifecycle obligations, ensuring clear, accurate, and compliant communication with the FDA and other external stakeholders. Driving writing standards, document governance, and cross-functional collaboration across PMI US and PMI Global.
Your 'day to day':
  1. Authoring Regulatory Documents
    1. Drafting and formatting complex FDA submissions (e.g., PMTA/MRTPAs, amendments, supplements, and postmarket reports) as well as responses to FDA Information Requests and Deficiency Letters, sometimes under tight timelines
    2. Creating supporting documents within submissions and ensuring scientific accuracy, internal consistency, and traceability to source data
    3. Aligning all documents with FDA law, regulations, and guidance documents
    4. Maintaining consistency with internal company policies
  2. Narrative Development & Data Integration
    1. Synthesizing complex scientific data into cohesive narratives that support regulatory strategy & product authorization
    2. Identifying data and information needed to support regulatory submissions, including types of studies, study designs, and data analysis, in collaboration with scientific SMEs
  3. Strategic Development & Implementation
    1. Identifying regulatory strategy and tactics to allow marketing of PMI products
    2. Identify complex, time-sensitive issues that prevent risk to submission readiness in a timely manner and facilitate resolution of issues
    3. Acting as regulatory SMEs, representing the US Regulatory Affairs Team in cross-functional project teams and ensuring alignment across PMI with evolving regulatory landscape

Who we're looking for:
  • Minimum 8 years of experience in regulatory affairs for tobacco, pharmaceuticals or other FDA-regulated products
  • Minimum 5 years of regulatory/scientific writing or evaluation of FDA applications for tobacco products
  • Extensive experience and leading role in regulatory writing projects (e.g., multi-module submissions, iterative engagement between FDA and applicants, cross-functional content integration)
  • Extensive knowledge and understanding of FDA's regulatory requirements for tobacco product submissions
  • Experience in leading regulatory writing
  • Mastery of regulatory document structures for FDA premarket applications and postmarket reporting as well as in-depth knowledge of FDA/CTP processes
  • Editorial excellence (structure, argumentation, data display, reference management) and plain-language communication
  • Advanced degree in a scientific discipline (e.g., PhD/ScD, PharmD, MS/MPH) or equivalent

Annual Base Salary Range: $176,000-$220,000
#LI-Hybrid #LI-JW1
What we offer
  • We offer a competitive base salary, annual bonus (applicable based on level of position), great medical, dental and vision coverage, 401k with a generous company match, incredible wellness benefits, commuter benefits, pet insurance, generous PTO, and much more!
  • We have implemented Smart Work, a hybrid model of working that promotes flexibility in the workplace.
  • Seize the freedom to define your future and ours. We'll empower you to take risks, experiment and explore.
  • Be part of an inclusive, diverse culture where everyone's contribution is respected; Collaborate with some of the world's best people and feel like you belong.
  • Pursue your ambitions and develop your skills with a global business - our staggering size and scale provides endless opportunities to progress.
  • Take pride in delivering our promise to society: To improve the lives of millions of smokers.

PMI is an Equal Opportunity Employer.
PMI is headquartered in Stamford, Conn., and its U.S. affiliates have more than 2,300 employees.
PMI has been an entirely separate company from Altria and Philip Morris USA since 2008. PMI's affiliates first entered the U.S. market following the company's acquisition of Swedish Match in late 2022. Philip Morris International and its U.S. affiliates are working to deliver a smoke-free future. Since 2008, PMI has invested $12.5 billion globally to develop, scientifically substantiate and commercialize innovative smoke-free products for adults who would otherwise continue to smoke with the goal of transitioning legal-age consumers who smoke to better alternatives. In 2022, PMI acquired Swedish Match - a leader in oral nicotine delivery - creating a global smoke-free champion led by the IQOS and ZYN brands. The U.S. Food and Drug Administration has authorized versions of PMI's IQOS electronically heated tobacco devices and Swedish Match's General snus as Modified Risk Tobacco Products and renewal applications for these products are presently pending before the FDA. For more information, please visit www.pmi.com/us and www.pmiscience.com.

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