Regulatory Consultant Salary at Whatsapp BETA

**What Business Development contributes to Cardinal Health** Business Development is responsible for identifying new sales opportunities and driving sales and services to new and existing clients. Responsible for maximizing client value/satisfaction by aligning complex product solutions and services with key client initiatives. Builds and maintains relationships with key decision makers and / potential influencers. **Job Summary** For nearly five decades, our industry-trained regulatory consultants have provided expertise and guidance to help pharmaceutical, biotechnology and medical device companies get their products to market. Our regulatory and product development strategies are designed to reduce the risk of failure and increase financial returns. We provide efficient scientific and regulatory consulting services throughout the full product lifecycle from molecular discovery to FDA approval & full commercialization to product retirement and generic intrusion. Cardinal Health Regul

CMC Statistician - Biotech/Pharma Employment Type: Contract or Permanent Location: Boston (USA-based candidates only) Compensation: Contract: $120-$200/hour (DOE) Permanent: $140,000-$180,000 base + benefits + bonus About the Opportunity iO Associates is supporting a growing biopharmaceutical company focused on the development of complex therapeutics requiring advanced Chemistry, Manufacturing, and Controls (CMC) strategies. As part of their continued expansion, they are seeking a candidate to lead/support in the design and analysis of analytical, manufacturing, and stability studies. Key Responsibilities Statistical design and analysis for CMC-related studies, including: Method validation Stability studies (e.g., shelf-life estimation, degradation modelling) Process validation and comparability Provide statistical input for regulatory submissions (IND, NDA, BLA) Support & partner with cross-functional teams to design DOE (Design of Experiments) and implement QbD (Quality by Design) st

Job Summary: Responsible for developing and implementing short and long term global regulatory strategies that support the success of investigational and marketed pharmaceutical products throughout their life cycle. The candidate will manage and lead submission related activities associated with the US and ex-US fillings for product, ensure timelines are appropriately managed and kept to, and issues are appropriately raised and resolved in a timely manner. Essential Duties and Responsibilities: (Include but not limited to the following. Other duties may be assigned) Serves as a liaison to FDA and provides strategic input with the regional regulatory leads responsible for ex-US regulatory activities. May provides oversight to regulatory consultants and vendors where applicable. Provides regulatory strategic support and guidance across all functions. Routinely performs regulatory precedence and competitive intelligence research. Contributes to identification of potential issues/gaps and

**What Business Development contributes to Cardinal Health** Business Development is responsible for identifying new sales opportunities and driving sales and services to new and existing clients. Responsible for maximizing client value/satisfaction by aligning complex product solutions and services with key client initiatives. Builds and maintains relationships with key decision makers and / potential influencers. **Job Summary** For nearly five decades, our industry-trained regulatory consultants have provided expertise and guidance to help pharmaceutical, biotechnology and medical device companies get their products to market. Our regulatory and product development strategies are designed to reduce the risk of failure and increase financial returns. We provide efficient scientific and regulatory consulting services throughout the full product lifecycle from molecular discovery to FDA approval & full commercialization to product retirement and generic intrusion. Cardinal Health Regul

About Us: Prom USA, Inc. is a global provider of innovative biocide solutions, dedicated to improving public health and safety across diverse industries. We are committed to delivering quality products while ensuring compliance with global regulatory standards. As we continue to grow and expand, we are looking for a dynamic and experienced Global Regulatory Affairs Director to lead our regulatory strategy across markets worldwide. Job Overview: As the Global Regulatory Affairs Director, you will be responsible for overseeing the development, implementation, and management of regulatory strategies to ensure our biocide products are in full compliance with applicable global regulatory frameworks. You will collaborate with internal and external stakeholders to navigate the complex landscape of biocide regulations, driving product approvals and market access globally. Your leadership will be key to shaping the company's regulatory affairs strategy and advancing the global reach of our prod

We are the leading provider of professional services to the middle market globally, our purpose is to instill confidence in a world of change, empowering our clients and people to realize their full potential. Our exceptional people are the key to our unrivaled, culture and talent experience and our ability to be compelling to our clients. You'll find an environment that inspires and empowers you to thrive both personally and professionally. There's no one like you and that's why there's nowhere like RSM. The Financial Examiner will primarily perform financial examinations and regulatory consulting services for state insurance departments. This position has significant opportunity for advancement as well as personal and professional growth. Responsibilities (Responsibilities vary depending on seniority level) Perform risk focused financial examinations to determine solvency and compliance to statutes on behalf of Risk & Regulatory Consulting LLC insurance clients. Perform reviews of ex

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. Due to our constant growth, we are looking for a Regulatory Affairs Specialist to support our projects in our office in Madrid (Spain) You will be responsible for: Execution of new registrations for our various product lines; Definition of regulatory strategies in compliance with the regulations of the countries where we operate; Coordination of activities related to the preparation of documents and regulatory submissions; Communication and collaboration with regulatory consulting firms to plan pre-submission approaches, compliance testing requirements, and follow-up of submissions to ensure regulatory compliance; Compilation and maintenance of regulatory databases or documentation systems; Support for local regul

Job Description: About Brown Brown University (https://www.brown.edu/about) is a leading research university distinct for its student-centered learning and deep sense of purpose. Our students, faculty and staff are driven by the idea that their work will have an impact in the world. Brown University offers a flexible work/life balance; summer hours, winter break and a comprehensive Benefits package including time off, annual paid holidays; benefits offerings including health, dental, vision, tuition assistance, retirement, wellness, employee discounts and more. To learn about Brown Universitys benefits, visit the University Human Resources web page here (https://www.brown.edu/about/administration/human-resources/benefits) for further information. About the Opportunity Brown HRPP is growing! As part of the BIRCH initiative (http://birch.brown.edu/) , Brown will soon be the main HRPP and Institutional Review Board (IRB) of record for Brown, Lifespan and Care New England health systems, a