Praca pharmacovigilance Warszawa

A leading pharmaceutical company in Warsaw is seeking a Senior Specialist to support operational regulatory pharmacovigilance. The successful candidate will maintain compliance with global standards and participate in cross-functional collaboration. Required qualifications include a Bachelor's or Master's degree in a related field and a minimum of 2 years in drug safety or pharmaceutical...

A global pharmacovigilance service provider is seeking a Senior Pharmacovigilance Officer, Team Lead with HCP and Clinical Trial experience. The candidate will be responsible for leading a team in ICSR management, ensuring efficient task distribution and workflow processes. Extensive pharmacovigilance experience along with excellent communication and organizational skills is required. The role...

We are looking for a Medical Information Officer to join our team in Poland HQ , supporting Theramex HQ UK Limited . In this role, you’ll act as the first point of contact for medical and scientific enquiries related to Theramex products, engaging with patients, healthcare professionals, and internal/external stakeholders. You will handle a wide range of medical information requests, ensure...

Graduate Pharmacovigilance Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Graduate Pharmacovigilance Associate to join our diverse and dynamic team....

Company Description: We are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. PrimeVigilance...

The opportunity Teva Pharmacovigilance unit is hiring a physician for the Safety physician, Director Pharmacovigilance role to join the Medical Scientific Unit (MSU) and support safety in projects under development. In this unit we lead drug safety across the entire Teva portfolio and throughout the product lifecycle. In partnership with other Teva stakeholders, our MSU safety physicians and...

Local Contact for Pharmacovigilance with Estonian and English language As the Local Contact for Pharmacovigilance, you will act as local contact for Pharmacovigilance for customers requiring the services for their product(s). This role can be conducted either Home Based / Hybrid / Office based from anywhere in Europe - the choice is yours. RESPONSIBILITIES • Respond fully and promptly to...

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and...

Principal Medical Scientist (Project Lead) - RWE - Poland, Bulgaria, Romania, Spain, UK - Sponsor-dedicated Updated: January 20, 2026 Location: Warsaw, MZ, Poland Job ID:25101745 Description Principal Medical Scientist (Project Lead) - RWE - Poland, Bulgaria, Romania, Spain, UK - Sponsor-dedicated Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to...

Regulatory Affairs Manager page is loaded## Regulatory Affairs Managerlocations: Warsaw, Polandtime type: Full timeposted on: Posted Todayjob requisition id: R1521462IQVIA is The Human Data Science Company. We use data, technology, analytics and human ingenuity to help healthcare clients deliver better solutions for patients and drive healthcare forward.Join our Regulatory Affairs and Drug...

Overview PSI is a leading Contract Research Organization with 30 years experience in the industry, offering a balance between stability and innovation to clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while...

Medical Monitor – Dermatology & Rheumatology, EU Medical Monitor Dermatology & Rheumatology, Europe: Germany, Spain or/and Poland 1 day ago – Be among the first 25 applicants The Medical Monitor provides medical and scientific support to clinical research programs. The role performs thorough data review to ensure data integrity and subject safety oversight, and communicates with sites,...

Overview Join Our Award-Winning Biopharmaceutical Company! Position Overview: We are looking for a Medical Affairs Manager (MAM) to manage medical activities within one or more therapeutic areas under the guidance of the Medical Director/TA Lead. The MAM will collaborate with marketing and market access teams while ensuring compliance with regulations and company policies. Responsibilities -...

Job Function Medical Affairs Group Job Sub Function Medical Affairs Job Category People Leader All Job Posting Locations Warsaw, Masovian, Poland Job Description expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in...

Join Natek as a Regulatory Process Coordinator and work for a top global pharmaceutical company ! This roles supports Process Directors and Associate Directors in managing key processes and projects. This is a mid-level position providing support in updating regulatory procedures within the ECMS system , performing administrative tasks such as updating SharePoint Online (SPOL) , and preparing...

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and...

Overview PrimeVigilance (part of Ergomed Group) is a specialised mid-size pharmacovigilance service provider established in 2008. We provide services within Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance, with staff across Europe, North America and Asia. We are focused on investing in our staff through training and development, valuing employee well-being and...

Company Description: We are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. PrimeVigilance...

Senior Pharmacovigilance Officer, Team Lead (HCP & Clinical Trial experience) Join to apply for the Senior Pharmacovigilance Officer, Team Lead (HCP & Clinical Trial experience) role at PrimeVigilance . We are PrimeVigilance (part of Ergomed Group), a specialised mid‑size pharmacovigilance service provider established in 2008. We pride ourselves on global organic growth year after year, with...

Job Description At PrimeVigilance, PV Officers are independent case processing team members who are expected to manage a variety of case processing services with full accountability. If you join PrimeVigilance, you can expect to work with teams of different sizes, from small clinical trial, to large, generic post-marketing teams. We are always looking for proactive, capable and motivated...