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Director, Site Start up

1 week ago
Serbia, Slovakia, Spain, United Kingdom, Hungary, Poland, Romania
Full-time
Lead
Program Manager
Project and Program Management
Apply Now
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
View All Jobs 80

Description

  • Provide leadership, guidance, and overall support to the Site Start-Up team across project delivery, communication, resources, procedures, systems, and processes.
  • Oversee site start-up delivery through direct management and cross-functional coordination of IRB/EC, Competent Authority, site contract, and budget activities.
  • Work with the Head of Site Start Up to define and evolve the SSU framework, including tools, methodology, intelligence, and risk mitigation.
  • Collaborate with Clinical Operations, project management, and other functions to plan, execute, and govern SSU activities globally and regionally.
  • Support corporate and departmental business strategies and act as an ambassador for change management during organizational growth.
  • Lead SSU programs, including large and highly complex programs, and manage escalations and remediation of SSU issues.
  • Optimize SSU processes and delivery to help achieve profitability and budget targets.
  • Partner with Global Resourcing to assess and manage team members and ensure cost, time, and quality goals are met.
  • Support career development, growth, succession planning, client meetings, presentations, proposals, budgeting, and bid defense preparation.
  • Develop, measure, and report SSU KPIs and drive continuous improvement.

Requirements

  • Bachelor’s degree in life sciences or a related field, or equivalent education, training, and experience.
  • Minimum 12 years of clinical research experience, including extensive site start-up experience.
  • Experience working for a Clinical Research Organization (CRO).
  • People management experience.
  • Expert knowledge of GCP/ICH guidelines and the clinical development process.
  • Demonstrated leadership track record.
  • Experience working in a team environment with resource management responsibility.
  • Experience with Microsoft Office products and clinical software such as CTMS, eTMF, and EDC.
  • Excellent communication, interpersonal, organizational, and attention-to-detail skills.
  • Proven experience in strategic planning, risk management, and change management.
  • Fluency in English.

Benefits

  • Remote work available in the UK, Spain, Poland, Hungary, Serbia, Slovakia, or Romania.
  • Equal Opportunity Employer status.
  • Reasonable accommodation available for candidates with disabilities during the application process.
  • Privacy policy protections for applicant data.

Interested in this position?

Apply directly on the company website

Apply Now

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