Sr. Clinical Trial Manager - Hybrid

Sr. Clinical Trial Manager - Hybrid Manufacturing/Labor Maple Grove, Minnesota Contract Apr 30, 2026 Sr. Clinical Trial Manager - Hybrid

Primary Location:

Maple Grove, Minnesota V-Soft Consulting is currently hiring for a Sr. Clinical Trial Manager - Hybrid for our premier client in Maple Grove, Minnesota. Education and Experience » Bachelor's degree in a scientific or healthcare discipline; advanced degree preferred. Experienced in: Renal denervation, Clinical trial management, People management of clinical trials and Cardiology Clinical trials. 10 years of experience in clinical research, including global clinical trials and vendor management. 5 years of demonstrated leadership experience managing and developing clinical trial staff, preferred. Strong understanding of

GCP, ICH

guidelines, and global regulatory requirements. Proven ability to manage complex timelines, budgets, and cross functional deliverables. Excellent communication, negotiation, and stakeholder management skills. Ability to navigate ambiguity, drive decision making, and influence across levels of the organization. Proven exposure and experience to internal audits and regulatory body audits. Ability to work in fast-paced environment requiring support of multiple studies and direct reports simultaneously.

WHAT YOU'LL DO

Job Responsibilities:

Lead, mentor, and develop Clinical Trial Managers and other assigned study personnel, fostering a high performance, collaborative team environment. Lead proactive risk identification, mitigation planning, and contingency management across assigned studies. Oversee end to end operational execution of global clinical trials, ensuring adherence to protocol, GCP, SOPs, and applicable regulatory requirements. Translate program strategy into operational plans, timelines, and resource needs; ensure cross functional alignment and timely delivery of study milestones. Manage CROs and external vendors, including selection, contracting, performance oversight, issue escalation, and budget tracking. Oversee development and maintenance of study documentation, including operational plans, study materials, systems, and regulatory submissions. Provide clear, data driven study updates, risk assessments, and recommendations to clinical leadership and governance bodies. Manage clinical trial budgets, including forecasting, accruals, variance analysis, and financial oversight of vendor contracts. Build and maintain strong relationships with investigators, clinical sites, and key opinion leaders to support enrollment, engagement, and study success. Champion continuous improvement in clinical operations processes, tools, and best practices. Ensure inspection readiness and compliance with internal quality standards, audit findings, and regulatory expectations. Interested? Qualified candidates should send their resumes to mjain@vsoftconsulting.com V-Soft Consulting Group is recognized among the top 100 fastest growing staffing companies in North America, V-Soft Consulting Group is headquartered in Louisville, KY with strategic locations in India, Canada and the U.S. V-Soft is known as an agile, innovative technology services company holding several awards and distinctions and has a wide variety of partnerships across diverse technology stacks. As a valued V-Soft Consultant, you're eligible for full benefits (Medical, Dental, Vision), a 401(k) plan, competitive compensation and more. V-Soft is partnered with numerous Fortune 500 companies, exceptionally positioned to advance your career growth. V-Soft Consulting provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.