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United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility.
This role can be done hybrid: 3 days per week from office in Warsaw.
Your Role
As a Senior Manager in Central Data Monitoring, you will lead the identification and communication of risk signals in clinical studies, collaborate with cross-functional teams to ensure data integrity, support risk-based quality oversight, develop applicable study plans, analyze data trends, contribute to risk review meetings, monitor corrective actions, oversee quality checks, and drive continuous improvement in central data monitoring processes.
Qualifications
* Advanced degree in Life Sciences or a related field.
* 7+ years of experience in central data monitoring, including experience in clinical data management, site monitoring or risk quality management.
* Strong knowledge of ICH GCP and regulatory requirements.
* Proficiency in data visualization and risk-based monitoring tools (e.g., CluePoints) and MS Office.
* Excellent analytical and problem‑solving skills.
* Effective communicator with leadership capabilities.
* Ability to manage multiple projects and priorities.
* Detail‑oriented and results‑driven mindset.
Benefits
* Health and well‑being: private medical care, life insurance, sports card, prepaid lunch card.
* Work‑life balance: additional paid days off, flexible working hours.
* Learning and development: co‑financing for language courses, trainings, certifications and other development opportunities.
Information on how we process your personal data for recruitment purposes can be found on the registration form in our Recruitment Portal.
Job Details
* Seniority level: Mid‑Senior level
* Employment type: Full‑time
* Job function: Research and Science
* Industries: Pharmaceutical Manufacturing
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