Director, Study Start Up-Poland

Premier Research Group

Polska

On-site

PLN 210,000 - 320,000

Full time

3 days ago
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Job summary

Premier Research Group is seeking a Director, Study Start Up-Poland to lead the SSU work within the Clinical Monitoring, Site Management and SSU team. You will oversee SSU performance in the region, manage staffing and resources, and drive timely project delivery.

The role requires strong experience in study start up, clinical trials, and regulatory knowledge across FDA, European procedures, and ISO14155 as applicable.

Qualifications

  • Bachelor’s degree, or international equivalent, in a clinical, scientific or health-related field.
  • 7–9 years of related health sciences experience, clinical trials support or pharma industry preferred.
  • Direct experience in study start up roles highly preferred.
  • 5–7 years of personnel management experience preferred.
  • Expertise in ICH/GCP and/or ISO14155 requirements and country-specific regulatory requirements.

Responsibilities

  • Provides immediate oversight for the SSU performance and teams within the assigned region/s.
  • Manages staffing and resources to ensure departmental utilization within region.
  • Drives SSU teams to meet project timelines.
  • Helps the SSU team improve knowledge, presentation skills and accountability.
  • Collaborates with VP to determine, improve and apply global efficiencies and processes for SSU.
  • Collaborates with SSU management in the US and other regions to align goals and objectives.
  • Ensures the SSU process is proactive and completed according to contractual agreements.
  • Applies principles of risk management.

Skills

Clinical trials experience
Study start up experience
People management

Education

Bachelor's degree in clinical/science/health field

Job description

Premier Research is looking for a Director, Study Start Up-Poland to join our Clinical Monitoring, Site Management and SSU team.

You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.

  • We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.
  • Your ideas influence the way we work, and your voice matters here.
  • As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.

Join us and build your future here.

What You'll Be Doing
  • Provides immediate oversight for the SSU performance and teams within the assigned region/s.
  • Manages staffing, and resources to ensure departmental utilization within region
  • Drives SSU teams to meet project timelines
  • Helps the SSU team to improve about their job knowledge, presentation skills and accountability.
  • Partners with VP to determine, improve, streamline, and apply global efficiencies and processes for SSU
  • Closely collaborates with the SSU mgmt. within the US and in other regions to work towards same goals, objectives in a consistent manner
  • Ensures that the SSU process is proactive and completed according to contractual agreement
  • Exercises principles of risk management
What We Are Looking For
  • Bachelor’s degree, or its international equivalent from an accredited institution, in a clinical, scientific or health related field
  • 7-9 years of related experience (health sciences); clinical trials support or pharmaceutical industry experience preferred
  • Direct experience in study start up roles highly preferred
  • 5-7 years of personnel management, oversight of larger groups preferred.
  • Expertise in ICH/GCP and/or ISO14155 requirements as well as detailed knowledge of the relevant country specific regulatory drug/device research and development requirements for conducting clinical trials
  • Working knowledge of FDA, European Regulatory and EC procedures as applicable
  • Knowledge of site and institution specific contract requirements
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