Praca zdalna: Nauka i badania

• Pełny etat
• Doświadczenie: 5-10 lat

Precision for Medicine seeks a Site Contracts Manager to join its European team, working fully remotely from Poland, Slovakia, Serbia, Romania or Hungary. The role focuses on drafting, reviewing, negotiating and tracking a range of clinical study agreements while partnering…

Poland

• Pełny etat
• Doświadczenie: 5-10 lat

Precision for Medicine seeks a Senior Clinical Project Manager with strong oncology experience to lead full‑service clinical trials (Phase I‑IV) on a global scale. You will own end‑to‑end project delivery, manage cross‑functional teams, and act as the primary liaison with clients…

Poland

• Pełny etat
• Doświadczenie: 5-10 lat

Precision for Medicine seeks a Principal/Senior Clinical Data Scientist to lead the clinical science function for Oncology, Rare Diseases, and Autoimmune programs from study start‑up through database lock. The role demands deep oncology expertise, hands‑on data review, and the…

Poland

• Pełny etat
• Doświadczenie: 2-5 lat

Candidates must hold a bachelor's degree in life sciences or a related field, with a pharmacy qualification being highly beneficial. Demonstrated experience in a regulatory or start-up role within a CRO or pharmaceutical industry is required, along with fluency in both Hungarian…

Poland

• Pełny etat
• Doświadczenie: 5-10 lat

Precision for Medicine is seeking experienced Senior Clinical Research Associates for a fully remote role (based in Poland) to support FSP partnerships with strategic sponsors across Europe. The role focuses on managing clinical trial sites, ensuring compliance with protocols and…

Poland

• Pełny etat
• Doświadczenie: 5-10 lat
• 190 200–285 400 zł / rok

Candidates must hold a bachelor's degree in a scientific or healthcare discipline and possess at least 5 to 7 years of regulatory experience within a CRO or pharmaceutical company. Strong knowledge of drug development processes, clinical trial methodology, and regulatory…

Poland

• Pełny etat
• Doświadczenie: 10+ lat

Precision Medicine Group seeks a Principal Biostatistician to lead statistical activities across all phases of clinical development. The role involves designing complex study protocols, authoring analysis plans, developing SAS programs, and providing expert statistical consulting…

Poland

• Pełny etat
• Doświadczenie: 2-5 lat

Precision Medicine Group is seeking an experienced Clinical Research Associate II / Senior CRA to work fully remote from Poland. You will independently monitor oncology sites, manage study portfolios, and influence study delivery while collaborating with CTMs and study teams. The…

Poland

• Pełny etat
• Doświadczenie: 5-10 lat

Precision Medicine Group seeks a Senior Clinical Project Manager – Oncology to lead full‑service clinical trials (Phase I‑IV) on a global scale. You will own end‑to‑end project delivery, manage budgets, timelines, scope and quality, and act as the primary liaison for clients and…

Poland

• Pełny etat
• Doświadczenie: 5-10 lat

Precision Medicine Group seeks a Principal/Senior Clinical Data Scientist to lead clinical science across Oncology, Rare Disease and Autoimmune programs from study start‑up through database lock. The role demands deep oncology expertise, data‑review acumen, and the ability to…

Poland

• Pełny etat
• Doświadczenie: 2-5 lat

Precision Medicine Group is seeking a Start Up Specialist fluent in Hungarian to support site start‑up activities across Central/Eastern Europe. The role involves preparing regulatory submissions, coordinating with ethics committees, and managing site activation documentation for…

Poland

• Pełny etat
• Doświadczenie: 5-10 lat

Precision Medicine Group is seeking experienced Senior Clinical Research Associates for a remote‑first role based in Poland (and other European locations). The role supports a dedicated FSP partnership, monitoring clinical trials, ensuring compliance with ICH‑GCP and SOPs, and…

Poland

• Pełny etat
• Doświadczenie: 5-10 lat
• 190 200–285 400 zł / rok

Precision Medicine Group, a CRO focused on oncology and rare disease, is seeking a Regulatory Manager or Senior Regulatory Manager to join its global team. The role involves shaping regulatory strategy, preparing high‑quality submissions, and guiding projects through the clinical…

Poland

• Pełny etat
• Doświadczenie: 2-5 lat

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Poland

• Pełny etat
• Doświadczenie: 2-5 lat

Labcorp, a global leader in laboratory services, seeks a remote Team Supervisor for Global Client Delivery on a 1‑year contract. You will lead a customer‑focused team in Poland, oversee day‑to‑day operations, drive continuous improvement, and ensure service excellence for our…

Warszawa, Pomeranian Voivodeship, Poland

• Pełny etat
• Doświadczenie: 2-5 lat
• 76 400–95 500 USD / rok

Westinghouse Electric Company seeks a remote Health Physicist to support radiation protection across more than 50 facilities in 19 countries. Reporting to the Senior Program Manager, Global Radiation Protection, you will collaborate with EHS professionals, site leadership, and…

Krakow, Lesser Poland Voivodeship, Poland

• Praca tymczasowa
• Doświadczenie: 10+ lat

Alphanumeric Systems seeks a Scientific Director (SERM & Clinical Safety & Pharmacovigilance) to lead safety evaluation, benefit‑risk management, and pharmacovigilance for global clinical and post‑marketing programs. The role is fully remote from Poland, supporting US/UK time…

Poland

• Pełny etat
• Doświadczenie: 10+ lat

Candidates must have strong CRO experience in Phase I-III clinical trials and in-depth knowledge of Oncology. A Bachelor's degree in a science or medical field is required, along with excellent communication and financial management skills.

Poland

• Pełny etat
• Doświadczenie: 5-10 lat

Join ICON plc’s sponsor‑dedicated team as a Senior Investigator Payment Associate, where you’ll lead end‑to‑end investigator payment operations for global clinical trials. You’ll leverage your expertise in pricing and payments to ensure accurate, compliant transactions, mentor…

Warsaw, Masovian Voivodeship, Poland

• Pełny etat
• Doświadczenie: 2-5 lat

Join ICON Strategic Solutions as a Clinical Study Assistant, supporting a pharmaceutical sponsor in day‑to‑day clinical trial activities. You’ll work within a sponsor‑dedicated model, collaborating with Clinical Operations, CROs and internal teams to ensure study readiness…

Warsaw, Masovian Voivodeship, Poland