Sr. Clinical Trial Manager
About the position
Let’s build the future of medicine - together. Join Enveda as a Senior Clinical Trial Manager in a remote capacity and help us transform natural compounds into life-changing medicines. We’re a team driven by curiosity and innovation - are you ready to make a difference? At Enveda, every role drives impact. As a Senior Clinical Trial Manager, you’ll be at the forefront of delivering hope to patients everywhere. Your expertise in clinical trial management will be critical in accelerating our mission to innovate drug discovery because every breakthrough starts with bold questions and brave actions.
Responsibilities
• Lead cross-functional trial teams to plan, execute, and deliver clinical trials in alignment with the development strategy, budget, and timeline
• Oversee CRO and vendor selection, management, and performance - including leading bid-defense processes, contracts, change orders, and quality oversight
• Author and review trial documents, SOPs, CRFs, and completion guidelines for internal and external 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 clinical trials, including CRO management and oversight in early phase studies
• 2+ years in a CRA role with direct 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 timely manner, with excellent written and verbal communication skills
• Proficiency in Microsoft Suite and clinical project management tools, with experience executing trials across multiple countries and regions
Benefits
• 90% Medical, Dental, Vision
• 401k Match
• Flexible PTO
• Adoption Assistance
Apply Now
Apply Now
Let’s build the future of medicine - together. Join Enveda as a Senior Clinical Trial Manager in a remote capacity and help us transform natural compounds into life-changing medicines. We’re a team driven by curiosity and innovation - are you ready to make a difference? At Enveda, every role drives impact. As a Senior Clinical Trial Manager, you’ll be at the forefront of delivering hope to patients everywhere. Your expertise in clinical trial management will be critical in accelerating our mission to innovate drug discovery because every breakthrough starts with bold questions and brave actions.
Responsibilities
• Lead cross-functional trial teams to plan, execute, and deliver clinical trials in alignment with the development strategy, budget, and timeline
• Oversee CRO and vendor selection, management, and performance - including leading bid-defense processes, contracts, change orders, and quality oversight
• Author and review trial documents, SOPs, CRFs, and completion guidelines for internal and external 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 clinical trials, including CRO management and oversight in early phase studies
• 2+ years in a CRA role with direct 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 timely manner, with excellent written and verbal communication skills
• Proficiency in Microsoft Suite and clinical project management tools, with experience executing trials across multiple countries and regions
Benefits
• 90% Medical, Dental, Vision
• 401k Match
• Flexible PTO
• Adoption Assistance
Apply Now
Apply Now