Praca zdalna: Nauka i badania

• Pełny etat
• Doświadczenie: 5-10 lat

We are looking for a Global Study Manager to join ICON’s Clinical Trial Management team. In this role you will design…

Warsaw, Masovian Voivodeship, Poland

• Pełny etat
• Doświadczenie: 2-5 lat
• 230 000–260 000 zł / rok

Candidates must have at least 2 years of direct site monitoring experience in the bio/pharma/CRO industry and a bachelor's degree in a science-related field. Proficiency in English and the local language, along with a current driver's license and the ability to travel 65%-75% of…

Poland

• Pełny etat
• Doświadczenie: 2-5 lat

Join ICON Strategic Solutions as a PK Medical Writer, where you’ll lead the creation of Clinical Pharmacology & Pharmacometrics documents for sponsor‑dedicated projects. In this senior role you’ll apply your scientific writing expertise to population PK/PD plans, reports…

Warsaw, Masovian Voivodeship, Poland

• Pełny etat
• Doświadczenie: 10+ lat

Join ICON plc’s Strategic Solutions team as a Senior Study Delivery Lead, driving global non‑interventional and interventional clinical studies from design through reporting. You’ll lead cross‑functional, matrixed teams, manage vendors, and ensure delivery to time, quality, and…

Warsaw, Masovian Voivodeship, Poland

• Pełny etat
• Doświadczenie: 5-10 lat

ICON Strategic Solutions is seeking a Senior Clinical Data Scientist with strong R and R Shiny expertise to turn complex clinical and real‑world data into intuitive applications and analytical solutions. You will collaborate with statisticians, data managers, programmers and…

Warsaw, Masovian Voivodeship, Poland

• Pełny etat
• Doświadczenie: 10+ lat

Premier Research seeks an Executive Director of Medical Affairs to lead scientific and medical support for biotech, medtech, and specialty pharma projects. You will engage key opinion leaders, guide operational teams, and represent the company at industry meetings, driving the…

Poland

• Pełny etat
• Doświadczenie: 2-5 lat

Premier Research seeks a Clinical Lead II – Neurology to join its Clinical Management team, supporting biotech, med‑tech, and specialty pharma partners in turning innovative ideas into new medicines, devices, and diagnostics. The role involves leading large clinical/SSU teams…

Poland

• Pełny etat
• Doświadczenie: 5-10 lat

Thermo Fisher Scientific is seeking a Safety Writer II to lead the planning, coordination, and delivery of safety writing deliverables for clinical trial and marketed product projects. In this regulated pharmacovigilance role you will manage low‑ to medium‑complexity reports…

Poland

• Pełny etat
• Doświadczenie: 5-10 lat

Requires a bachelor's degree in a clinical, science, or health-related field and at least 5 years of relevant experience. Candidates must possess strong technical aptitude, excellent communication skills, and the ability to work effectively in a fast-paced environment.

Poland

• Pełny etat
• Doświadczenie: 10+ lat

Thermo Fisher Scientific is seeking a Project Manager / Sr. Project Manager to lead cross‑functional, multi‑country clinical projects. The role serves as the primary sponsor contact, overseeing delivery of quality, time, and cost objectives while managing risk, finances, and…

Poland

• Praca tymczasowa
• Doświadczenie: 2-5 lat

Join LEO Pharma in Gdańsk as a Global Patient Safety Specialist, where you will ensure Individual Case Safety Reports and Adverse Drug Events are processed and submitted accurately and on time. You will work with a dynamic team focused on drug safety and regulatory compliance…

Gdansk, Pomeranian Voivodeship, Poland

• Pełny etat
• Doświadczenie: 10+ lat

Parexel seeks a Senior Regulatory Affairs Manager/Consultant with over 10 years of regulatory experience and CMC expertise to drive CMC writing, variation strategies, and client projects across Europe. The role focuses on scientific rationale development, project leadership, and…

Warsaw, Masovian Voivodeship, Poland

• Pełny etat
• Doświadczenie: 10+ lat

ICON plc seeks a Senior Clinical Trial Manager (Study Delivery Lead) to lead and drive cross‑functional teams on global non‑interventional studies. Based in ICON’s sponsor‑dedicated model, you will oversee end‑to‑end design, execution and reporting of retrospective and…

Warsaw, Masovian Voivodeship, Poland

• Pełny etat
• Doświadczenie: 10+ lat

ICON plc seeks a senior Clinical Trial Manager to lead non‑interventional studies (NIS) within its sponsor‑dedicated model. You will drive cross‑functional teams globally, overseeing end‑to‑end design, execution, and reporting of retrospective and prospective NIS projects. The…

Warsaw, Masovian Voivodeship, Poland

• Pełny etat
• Doświadczenie: 5-10 lat

ICON plc, a global healthcare intelligence and clinical research organisation, seeks a Senior Global Regulatory Affairs Specialist to design and analyse clinical trials, interpret complex medical data, and drive innovative treatments. The role demands ownership of regulatory…

Warsaw, Masovian Voivodeship, Poland

• Pełny etat
• Doświadczenie: 2-5 lat
• 220 000–240 000 zł / rok

Dołącz do Parexel jako Clinical Research Associate, współpracując z zespołem FSP w północnej Polsce. Będziesz kluczowym kontaktem dla ośrodków badawczych, zapewniając ich gotowość, monitorowanie oraz zgodność z ICH‑GCP i regulacjami lokalnymi. Praca wymaga samodzielności, podróży…

Poland

• Pełny etat
• Doświadczenie: 5-10 lat

Join Worldwide Clinical Trials as a Manager, Regulatory Affairs (EMEA) to lead regulatory submissions across EMEA, Asia Pacific and Latin America. You’ll guide study budgets, support business development, and mentor junior staff while ensuring compliance with global standards…

Warsaw, Masovian Voivodeship, Poland

• Pełny etat
• Doświadczenie: 2-5 lat

Requires a bachelor's degree or RN in a related field along with knowledge of ICH-GCP guidelines and regulatory requirements. Candidates must possess excellent communication skills and the ability to manage travel up to 75%.

Poland

• Pełny etat
• Doświadczenie: 10+ lat

Precision for Medicine is seeking a Principal Biostatistician to lead statistical activities across all phases of clinical development. The role involves designing and reviewing protocols, creating analysis plans, developing SAS programs, and serving as a global statistical…

Poland

• Pełny etat
• Doświadczenie: 2-5 lat

Precision for Medicine seeks an experienced Clinical Research Associate II / Senior CRA to work remotely from Poland, managing oncology clinical trial sites from initiation to close‑out. The role demands independent monitoring, strong patient safety and data integrity focus, and…

Poland