Remote Senior Clinical Trials Project Manager

closed
Logo of pfm medical, inc.

pfm medical, inc.

πŸ’΅ $125k-$187k
πŸ“Remote - United States

Job highlights

Summary

Join Precision for Medicine as a Senior Clinicals Trial Project Manager to plan, direct, coordinate, and deliver activities for designated clinical-study projects.

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, among other benefits
This job is filled or no longer available