Drug Development
Regulatory Affairs.
Drug Development.
Regulatory Affairs.
Within Life Sciences, Regulatory Affairs is an essential and ever-evolving field. It is an integral part of the drug development process, providing oversight and guidance to ensure that products are safe and effective. The role of Regulatory Affairs Professionals is to facilitate the development and approval of products in compliance with global regulations.
At i-Pharm, we support our clients throughout the entire drug development lifecycle, with Regulatory Affairs Professionals playing an essential role in helping bring safe and effective products to market quickly and efficiently.
How we can help.
As we focus on the life science industry, our team of Regulatory Affairs recruiters are specialists in their field.
They are experts in discovering new talent and integrating them into the efforts of the safety and efficacy of the drug development process.
At i-Pharm, we have been supporting some of the world’s largest Pharmaceutical, Biotech, Medical Device and Contract Research Organisations (CROs) with Regulatory Affairs Clinical Trials, CMC, Post-Licensing, Labelling, and Medical Devices staffing since 2008.
Over the last 15 years, it has been our mission to recruit regulatory affairs professionals across all forms of life science. The Regulatory Affairs department plays a critical role in the development of NCEs, biologics and medical devices by ensuring companies comply with the regulations and laws specific to the sector.
We understand the unique challenges of recruiting in this complex area, which is why we want the best talent walking through our doors, so we can match them with their perfect placement.
For our candidates, we listen to your aspirations and tailor our search to find you the best regulatory affairs job to take your career forward.
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Discover your dream job with us. We can help you with advice and support to find the right place for you.
Global Reach.
With Regulatory Affairs recruitment teams expanding across the globe, we have crafted an extensive network of clients and candidates. Our offices in Europe, USA and Australia have provided us with the opportunity to recruit top-level talent within the Regulatory Affairs space. Thanks to this global reach, we have been able to develop our local team’s understanding of the market and benefit from a large pool of talent.
Market Specialists.
Our team is fully dedicated to recruiting within the Regulatory Affairs space, providing support throughout the drug development life cycle from clinical trials to market authorisation.
As we are experienced recruiters, with 15 years of experience, you’ll always be dealing with a functional specialist, who’ll be able to understand your niche and provide you with unique insights into the current market.
Whether you are looking for a permanent placement or a contract role, we can help you find your perfect match!
Take a look through the latest job postings.
Latest Jobs in Regulatory Affairs.
Our Regulatory Affairs Specialists.
Our Specialisms.
We work across the Pharmaceutical, Biotech and MedTech sectors, with a particular focus on the following specialist areas.
Biometrics
We are specialists at recruiting talent in the Biometrics space, supporting the leading global CROs, Pharmaceutical and Biotechnology companies with sourcing Biostatisticians, Statistical Programmers, Clinical Data Managers and SAS Programmers.
Clinical
Clinical Operations is at the heart of what we do. We support some of the world’s largest CROs and Bio-Pharma companies sourcing Clinical Research Associates for international clinical trials across Phases I to IV.
Commercial
Our experienced Commercial Recruitment Teams support the leading CROs, Pharmaceutical and Biotechnology companies with sourcing sales and marketing specialists in Account Management, Fields Sales, Medical Sales, Market Access and Business Development.
Medical & Scientific
Our specialist teams support the leading Pharmaceutical, Biotech, and Contract Research Organisations with staffing in the Medical & Scientific space, in areas such as Medical Affairs, Medical Writing, Drug Safety and specialist scientists.
Quality Assurance & Tech Ops
Our specialist Quality Assurance and Technical Operations teams focus on a broad range of roles across Good Manufacturing Practice (GMP), Good Clinical Practice (GCP) and Good Laboratory Practice (GLP), as well as Supply Chain, Logistics and a range of Engineering roles.
Regulatory Affairs
Our specialist Regulatory Affairs teams support the leading Pharmaceutical, Biotech, and Contract Research Organisations with staffing in the Regulatory Affairs space, throughout the whole product life cycle from research to approval, through to commercialisation.
Want to launch your career in Regulatory Affairs?
If you are looking to begin or advance your career in the Regulatory Affairs sector, why not discuss your options with us? We want to be your career partner, the place that you turn if you have questions, queries or expectations that need to be answered.
You can contact us in any of our offices across the world for Regulatory Affairs positions by going through our contact page.
