Director, Site Startup

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Precision Medicine Group

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

• Provide leadership, guidance and overall support to the Site Start-up team across project delivery, communication, human resources, revenue enhancement, procedures, systems and processes • Support management of site start-up delivery through direct management and cross-functional oversight of IRB/EC, Competent Authority submissions, site contracts, budget negotiations and other start-up requirements • Establish the SSU framework with the Head of Site Start Up, including intelligence, tools, methodology, risk evaluations and mitigations • Support global and regional collaboration with Clinical Operations, project management and other cross-functional departments • Support corporate and departmental business strategies and act as an ambassador for change management • Provide leadership and oversight on large and increasingly complex SSU programs • Manage escalations and remediation of SSU concerns • Optimize processes and delivery to meet or exceed budget targets • Partner with Global Resourcing on team-member assessment and management • Support team career development, growth and succession planning while ensuring policy and regulatory compliance • Coordinate SSU Lead participation in client meetings and presentations • Collaborate with Business Development on opportunities, proposals, budgeting and bid defenses • Support project strategy, SSU delivery and project evaluations • Develop, measure and report SSU KPIs and lead continuous improvement • Reinforce company culture and values, motivate the team, maintain engagement and drive retention

🎯 Requirements

• Bachelor's degree in life sciences or related field, or equivalent combination of education, training and experience • Minimum 12 years of clinical research experience, including extensive Site Start-up experience • Experience working for a Clinical Research Organisation (CRO) • Experience in people management • Expert knowledge of GCP/ICH guidelines and the clinical development process • Demonstrated leadership track record • Experience working in a team environment with resource management experience • Experience with Microsoft Office products: Outlook, Word, Excel and PowerPoint • Clinical software experience, including CTMS, eTMF and EDC • Excellent communication and interpersonal skills • Excellent organizational skills, attention to detail and customer service demeanor • Proven strategic planning, risk management and change management experience • Fluency in English

🏖️ Benefits

• Discretionary annual bonus • Private medical insurance • MultiSport Card • Life insurance • Pension • Home working allowance • Vacation • Other benefits

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