Project Director

🔥 18 hours ago

🌐 Romania, United Kingdom, +5 more countries – Remote

🇷🇴 Romania – Remote 🇬🇧 United Kingdom – Remote 🇪🇸 Spain – Remote 🇵🇱 Poland – Remote 🇭🇺 Hungary – Remote 🇷🇸 Serbia – Remote 🇸🇰 Slovakia – Remote

⏰ Full Time

🔴 Lead

👔 Director

👻 Ghost score 20%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Precision Medicine Group

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2012

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 $35.2M Venture Round on 2021-03

Consulting • Healthcare • Logistics

Precision Medicine Group is a global team of experts that specializes in precision medicine, which combines advanced lab sciences, translational informatics, regulatory affairs, payer insights, and marketing communications. The company focuses on overcoming product development and commercialization challenges for pharmaceutical and life sciences clients. Their services include biomarker-driven research and development, as well as commercialization support for life science organizations from launch to product maturity. Precision Medicine Group operates through two main arms: Precision for Medicine and Precision AQ, specializing in clinical and commercial solutions respectively.

📋 Description

• Serve as the primary client point of contact and participate in proposal activities and client presentations • Oversee all aspects of clinical research trials and assigned portfolios • Direct project managers through project establishment, planning, initiation, procurement, execution and closing • Manage study budgets, scope, change orders and financial health • Oversee project profitability, billable hours, billing and forecasting • Develop or oversee comprehensive project plans, timelines, risk management and mitigation • Ensure quality management, eTMF inspection readiness and corrective/preventive actions • Establish tracking metrics for trial and team progress • Prepare project status updates, KPI reports and solutions for clients and senior management • Lead internal and client meetings and advance study-level strategies • Oversee cross-functional project teams and trial execution • Communicate protocol and study issues and implement necessary actions • Conduct formal presentations, including bid defenses • Ensure study-specific training and compliance • Support business development and marketing activities, including bid defense travel • Mentor associate, project and senior project managers • Contribute to departmental updates and company SOP development • Provide ongoing feedback and annual performance reviews for functional team members • Identify project-level performance problems and ensure corrective action • Perform assigned duties and administrative tasks, including training and time reporting

🎯 Requirements

• Degree or equivalent combination of education/experience in a science or health-related field for EU candidates; advanced degree preferred • Minimum of 8 years of clinical research experience or proven competencies for the position • Minimum of 5 years of direct project management experience • High proficiency with Microsoft Office Products (Outlook, Word, Excel, PowerPoint), Microsoft Project, eTMF, EDC and CTMS • Excellent communication and interpersonal skills • Excellent organizational skills and attention to detail • Customer service orientation • Experience managing highly complex and global studies or a portfolio of studies • Mastery knowledge of ICH-GCP and relevant Precision SOPs • Excellent knowledge of project management techniques and tools • Highly experienced in cross-functional project management environments • Strong understanding of cross-functional management • Strong understanding and demonstrated expertise in project planning, risk management and change management • Highly experienced in pharmaceutical and/or device research • Demonstrated excellence in time management, negotiation, critical thinking, decision making, analytical, interpersonal, presentation, verbal and written communication skills • Expert understanding of project management software • Highly developed customer orientation, influence, negotiation and conflict management skills • Ability to work and plan independently and in a team environment • Ability to travel domestically and internationally, including overnight stays

🏖️ Benefits

• Supportive and collaborative environment • Work-life balance • Team development opportunities • Employee appreciation for contributions • Equal opportunity employment • Reasonable accommodation during the application process