Project Director

2 hours, 38 minutes ago
Full-time
Lead
Project and Program Management
Precision For Medicine

Precision For Medicine

Precision for Medicine is a specialized scientific services company that helps pharmaceutical and life sciences clients innovate, develop, and commercialize next-generation medical products. With a diverse team of experts, they offer comprehensive serv...

Pharmaceuticals
1K-5K
Founded 2012
$225M raised

Description

  • Serve as the primary client liaison, supporting proposals, presentations, and bid defenses.
  • Oversee global clinical trials or portfolios from planning and initiation through execution and closeout.
  • Direct project managers and cross-functional teams, setting expectations and driving study strategies.
  • Manage study scope, budgets, profitability, billing, forecasting, change orders, and financial health.
  • Develop and oversee project plans, timelines, risk mitigation, and change management activities.
  • Ensure quality management, eTMF inspection readiness, corrective actions, and training compliance.
  • Establish progress metrics and provide status updates, KPIs, solutions, and recommendations to clients and senior leadership.
  • Lead internal and client meetings and communicate protocol issues, deviations, and required actions.
  • Mentor project management staff, provide performance feedback, and support operational improvements and SOP development.
  • Travel domestically and internationally, including overnight stays, as required.

Requirements

  • Degree or equivalent education and experience in a science or health-related field; advanced degree preferred.
  • At least 8 years of clinical research experience and 5 years of direct project management experience, or demonstrated equivalent competency.
  • Experience managing highly complex global studies or portfolios of studies.
  • Highly experienced in pharmaceutical and/or medical device research.
  • Proficiency with Microsoft Office, Microsoft Project, eTMF, EDC, CTMS, and project management software.
  • Mastery of ICH-GCP and applicable clinical research SOPs.
  • Strong knowledge of project planning, risk management, change management, and cross-functional management.
  • Excellent communication, presentation, organizational, analytical, negotiation, decision-making, and interpersonal skills.
  • Ability to lead, motivate, influence, and resolve conflicts within cross-functional study teams.
  • Ability to work independently and collaboratively with a strong focus on accountability and continuous improvement.

Benefits

  • Fully remote work from the UK, Spain, Poland, Hungary, Romania, Serbia, or Slovakia.
  • Supportive, collaborative environment focused on work-life balance and team development.
  • Opportunity to contribute to clinical research for novel oncology and rare-disease therapies.
  • Equal opportunity employer with reasonable accommodation support for applicants with disabilities.

Interested in this position?

Apply directly on the company website

Apply Now

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