Regulatory Specialist (Efficacy & Field Trials)

French Speaking Efficacy Dossiers & Trials Coordinator – Biological Assessment Dossiers (BADs) - work from anywhere in Europe.A specialist agrochemical company is looking for an experienced Efficacy Dossiers & Trials Coordinator to join a small, multicultural and entrepreneurial team. This is a technically focused role sitting at the intersection of field development and European regulatory compliance.The RoleYou will be responsible for writing and supporting Biological Activity Dossiers (BADs) and dRR Section B3 submissions, alongside conceiving, monitoring and interpreting field trials. You'll work closely with a range of collaborators and customers — including key French-speaking contacts — requiring strong communication skills and cultural adaptability.What You'll NeedA minimum of 2-3 years' field development experience within the European plant/crop protection industry, gained either within a multinational agrochemical company or a sizeable CRODemonstrable competency in writing BADs and dRR Section B3A solid understanding of EU regulatory requirements at both pan-EU and country levelKnowledge of field trials procedures and protocols in at least one European Regulatory ZoneDegree-level qualification (or higher) in Agronomy, the Biological Sciences or Agricultural SciencesFluent English is essential; French fluency (or a strong working base with willingness to develop quickly) is requiredNice to HavePostgraduate qualificationKnowledge of registration data requirements in markets outside Europe, particularly Africa and the Middle EastTo ApplySend your CV in confidence to thsi advert of email Abid Kanji on a.kanji@nonstopconsulting.com