Job Description
📋 Description Coordinate nonclinical regulatory activities across product lifecycle to ensure readiness for Partner with scientists, regulatory experts, and cross-functional stakeholders to deliver Manage timelines, communications, and deliverables to translate regulatory strategies into Provide operational support bridging scientific, regulatory, and operational functions. Develop and maintain SOPs, templates, and guidance materials; drive process improvements. Monitor progress, identify risks, and support mitigation strategies to maintain timely deliverables. 🎯 Requirements Master’s degree required, or equivalent combination of education/experience; or Bachelor’s with 2 Experience supporting pharmaceutical research, biotechnology, life sciences, or nonclinical drug Understanding of nonclinical development processes, regulatory documentation requirements, and Experience coordinating complex cross-functional projects; strong project management Ability to build collaborative relationships and influence stakeholders without direct authority. Excellent organizational and multi-tasking skills; strong written/verbal/interpersonal 🎁 Benefits Competitive annual salary range of approximately $101,675 - $137,561 USD, depending on experience Comprehensive healthcare benefits, including medical, dental, and vision coverage. Retirement savings plan with company contributions. Flexible spending account options and financial wellness resources. Annual bonus opportunities based on eligibility. Stock-based long-term incentive opportunities.
