European Regulatory & Field Sciences Lead – Remote

Yahoo! Inc.; Dublin; On-site; EUR 90,000 - 120,000; Full time

Job summary

Oath, a public benefit company, is seeking a Regulatory Affairs & Field Sciences Manager for Europe, based in Dublin or remote from Europe. You will lead regulatory strategy to secure FTO for Oath Soil Life and coordinate field trials with CROs and partners across Europe, UK, Turkey, and the Middle East.

Reporting to the BD Lead Europe, you will manage submissions, compliance, and stakeholder communications, driving regional trial programs and ensuring timely data delivery.

Qualifications

• Minimum 5-7 years of relevant experience in Regulatory Affairs within the agricultural sector.
• Demonstrated experience in European regulatory affairs, particularly using EU Mutual Recognition and legacy national abiotic registration processes.
• Comprehensive grasp of the scientific protocols and prerequisites for field-based research.
• Field trial experience highly desirable
• Degree in Agronomy or a related field

Responsibilities

• Develop regulatory strategy for Europe, prioritizing MR directive to gain FTO.
• Manage product registration processes and submissions to regulatory bodies.
• Oversee regulatory compliance across Europe, UK, Turkey and the Middle East.
• Coordinate with regulatory agencies or local contractors to secure approvals.
• Monitor changes in European regulations and update strategies accordingly.
• Document submissions and reports for stakeholders and BD activities.

Skills

Regulatory affairs

European regulations

Field trials

Communication skills

Cross-functional teamwork

Education

Degree in Agronomy

Job description

Oath, a public benefit company, is seeking a Regulatory Affairs & Field Sciences Manager for Europe, based in Dublin or remote from Europe. You will lead regulatory strategy to secure FTO for Oath Soil Life and coordinate field trials with CROs and partners across Europe, UK, Turkey, and the Middle East.

Reporting to the BD Lead Europe, you will manage submissions, compliance, and stakeholder communications, driving regional trial programs and ensuring timely data delivery.