Precision Medicine Group is hiring a
Senior Clinical Trials Project Manager

Summary

Join us today as a Senior Clinicals Trial Project Manager to plan, direct, coordinate, and deliver activities for designated clinical-study projects to ensure that project objectives of quality, scope, cost, and time are accomplished.

Requirements

• Bachelor’s degree or equivalent combination of education/experience in science or health-related field. Advanced degree preferred
• Minimum of 7 years of clinical research experience or proven competencies for this position and a minimum of 3 years of direct project management experience
• Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint) Microsoft Project
• Excellent communication and interpersonal skills to effectively interface with others in a team setting
• Excellent organizational skills, attention to detail, and a customer service demeanor
• Ability to travel domestically and internationally including overnight stays

Responsibilities

• Serve as primary point-of-contact and primary escalation point to the client
• Coordinate and oversees all functional services including external vendors to the established timeline and budget
• Manage the study budget, ensuring project remains within scope and that any out of scope activities are identified and handled as appropriate
• Develop robust and comprehensive project plans, including timelines, to guide all parameters of trial execution with consistency and quality
• Maintain integrated collaboration with clinical operations in the delivery and participates in clinical activities as appropriate
• Establish tracking metrics to monitor trial and team progress towards project goals
• Prepare project status updates and report on progress to clients and senior management, offering solutions and opportunities as they arise
• Leads team meetings with the client and sets expectations for the project team
• Communicate effectively with client and Precision management to relay protocol/study issues including any deviations and implements necessary actions in response to those issues
• Travel as necessary according to project needs
• Mentor, train, and supervise staff at a functional level
• Assist with review of clinical study reports
• Support business development and marketing activities as appropriate
• Perform other duties as assigned by management
• May participate in review of protocols and other study documentation
• Provides on-going feedback, development and coaching for functional team members including annual performance reviews

Preferred Qualifications

• Advanced degree
• Experience in managing complex and global trials

Benefits

• Health insurance
• Retirement savings benefits
• Life insurance and disability benefits
• Parental leave
• Paid time off for sick leave and vacation