Project Director

🔥 14 hours ago

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

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

⏰ Full Time

🔴 Lead

👔 Director

👻 Ghost score 10%

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 For Medicine

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

💰 $75M Private Equity Round on 2015-12

Healthcare • Consulting • Logistics

Precision For Medicine is a leading organization that specializes in supporting the development and commercialization of innovative therapies, particularly in oncology, rare diseases, and autoimmune conditions. With a comprehensive range of services including clinical trial management, lab services, and biospecimen collection, they integrate advanced biomarker capabilities and manufacturing solutions to streamline the complex clinical development processes. Their mission is to accelerate research and bring life-changing medical solutions to patients by overcoming traditional inefficiencies typically found in the pharmaceutical development landscape.

📋 Description

• Serve as 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 closeout • Manage study budgets, scope, change orders and project profitability • Oversee billable hours, billing compliance and forecasting • Develop or oversee comprehensive project plans, timelines, risk management and mitigation strategies • Ensure quality management, eTMF inspection readiness, quality notifications and CAPA plans • Establish tracking metrics for trial and team progress • Prepare project status updates, KPI reports and presentations for clients and senior management • Lead internal and client meetings and drive study-level strategies • Oversee cross-functional project teams and trial execution • Communicate protocol and study issues and implement corrective 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 • Complete training, time reporting and administrative duties • Perform other duties assigned by management

🎯 Requirements

• Degree or equivalent combination of education/experience in 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 • Highly proficient with Microsoft Office Products (Outlook, Word, Excel, PowerPoint), Microsoft Project, eTMF, EDC and CTMS • Excellent communication and interpersonal skills • Excellent organizational skills, attention to detail, and customer service demeanor • Experience managing highly complex and global studies or a portfolio of studies • Mastery 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 of project planning, risk management and change management • High level of integrity and professional and ethical standards • Ability to lead and inspire study teams • Demonstrated excellence in time management, negotiation, critical thinking, decision making, analytical, presentation, verbal and written communication skills • Expert understanding of project management software • Highly experienced in pharmaceutical and/or device research • Expertise in strategic planning, risk management and change management • 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 encouragement • Equal Opportunity Employer • Reasonable accommodation available for applicants with disabilities