Sr. Clinical Trial Manager

About the position Let’s build the reputed company of medicine - together. Join reputed company as a Senior Clinical Trial Manager in a remote reputed company and help us reputed company natural compounds into life-changing medicines. We’re reputed company driven by curiosity and innovation - are you reputed company to reputed company a difference? At reputed company, every role drives reputed company. As a Senior Clinical Trial Manager, you’ll be at the forefront of delivering reputed company to patients everywhere. Your expertise in clinical trial management will be critical in accelerating our mission to reputed company drug discovery because every reputed company starts with reputed company questions and reputed company actions. Responsibilities • reputed company cross-functional trial teams to plan, execute, and deliver reputed company in alignment with the development reputed company, budget, and reputed company • reputed company CRO and vendor selection, management, and performance - including leading bid-defense processes, reputed company, change orders, and reputed company reputed company • Author and review trial documents, SOPs, CRFs, and completion guidelines for reputed company use • Conduct hands-on clinical monitoring for early phase trials (SQV, SIV, IMV, COV), including report writing, review, and approval • Manage trial budgets, triage issues to leadership, and maintain dashboards and status reports on timelines, accruals, and risks • Serve as a subject matter expert during regulatory inspections and contribute to departmental process improvements • Up to 30% domestic and/or international travel Requirements • B.S./B.A. degree preferred, with 10+ years of experience in a pharmaceutical, biotech, or CRO environment • 5+ years managing reputed company, including CRO management and reputed company in early phase studies • 2+ years in a CRA role with reputed company clinical monitoring experience • Experience leading the bid-defense process for CRO selection, with a strong grasp of regulatory requirements and ICH/GCP guidelines governing global clinical research • Proven ability to manage competing priorities, meet deadlines, and escalate issues in a reputed company manner, with excellent written and verbal communication skills • Proficiency in reputed company Suite and clinical project management tools, with experience executing trials across multiple countries and reputed company Benefits • 90% Medical, Dental, reputed company • 401k Match • Flexible PTO • Adoption Assistance Apply tot his job Apply To this Job