Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Precision For Medicine

Director, Site Start Up

Precision For Medicine

Director leading site start-up operations for Precision for Medicine, a global clinical research services organization. Overseeing SSU strategy, delivery, compliance, teams, and continuous improvement across European markets.

Posted 8/5/2026full-timeRemote • 🇵🇱 PolandLead💰 PLN 402,700 - PLN 604,100 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates extensive expertise in Site Start-up processes within clinical research, including leadership in project delivery, risk management, and compliance with GCP/ICH guidelines. Proven ability to optimize operations, manage cross-functional teams, and drive strategic initiatives to enhance profitability and efficiency.

Highest-signal resume keywords
Site Start-Up ExperienceGCP/ICH Guidelines ExpertiseClinical Research Organisation (CRO) ExperiencePeople ManagementStrategic Planning

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical ResearchSite Start-UpRisk ManagementChange ManagementBudget NegotiationKPI DevelopmentProcess OptimizationRegulatory ComplianceProject ManagementResource Management
Soft Skills
LeadershipCommunicationInterpersonal SkillsOrganizational SkillsAttention to Detail
Tools & Technologies
Microsoft OfficeCTMSETMFEDC
Industry Keywords
Clinical Development ProcessSite ContractsIRB/EC SubmissionsCompetent Authority SubmissionsChange Management

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • 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 submissions, Competent Authority submissions, governing organizations, 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 evaluation, and mitigation
  • Coordinate SSU activities with Clinical Operations, project management, and other cross-functional departments globally and regionally
  • Support corporate and departmental business strategies and act as an ambassador for change management
  • Provide leadership and oversight for large and increasingly complex SSU programs
  • Manage escalations and remediate SSU concerns
  • Optimize processes and delivery to support profitability and budget targets
  • Partner with Global Resourcing teams to assess and manage SSU team members and meet cost, time, and quality goals
  • Support career development, growth, succession planning, policy, and regulatory compliance
  • Support SSU Lead participation in client meetings and presentations
  • Collaborate with Business Development on opportunities, proposals, budgeting, and bid defense
  • Support project strategy, delivery, evaluations, and required changes
  • Develop, measure, and report SSU KPIs and lead continuous improvement
  • Reinforce company culture and values, motivate the team, maintain engagement, and drive retention

Requirements

What you’ll need
  • Bachelor's degree in life sciences or related field, or equivalent combination of education, training, and experience
  • Minimum 12 years of experience in clinical research, 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 orientation
  • Proven experience in strategic planning, risk management, and change management
  • Fluency in English

Benefits

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