Regulatory Documents Jobs in Poland

Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthrou...

Would you like to work with products that actually change the lives of people worldwide and do it in a fast-growing company Then we can offer you the right challenge! Right now we are looking for a dedicated and skilled Junior Homologation Specialist to support Demant. If you already have experienc...

Introduction:TheAssociate Director Senior Patient Safety Scientistrole leads the review of safety data and related documents for potential safety issues in collaboration with the Global Safety Physician (GSP) and (Associate) PV Scientist.He/she authors and leads PV input to safety documents and regu...

Location: Warsaw / HybridAbout You You hold a Bachelors or Masters degree in Life Sciences. You bring a minimum of 2 years experience in Case Processing and/or Drug Safety/Pharmacovigilance with solid knowledge of global PV regulations. You are detailoriented organised confident with medical termino...

Location: Warsaw / HybridAbout You You hold a BSc or MSc in Life Sciences. You bring over 5 years experience in Drug Safety/Pharmacovigilance with strong understanding of global PV regulations and GVP modules. You have a proven track record in planning and authoring safety documents (e.g. PSURs RMPs...

The GSA is a member of extended global study team supporting delivery of clinical studies within Late Development Oncology (LDO) to time cost and quality from Clinical Study Protocol (CSP)development through study set-up maintenance close-out development of Clinical Study Report (CSR) to study archi...

Job OverviewUnder general supervision perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include main...

The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICH-GCP protocol requirements within Study specific defined timelines and enrollment goals.The function of the role may include but not limited to any/all of the following:Act as...

We are currently looking for Banking Regulatory Compliance for our UAE operations with the following Skill set and terms & conditions. Education & Qualifications: Tertiary education with a Bachelors degree as a minimum.Any Compliance qualification or certification such as ACAMS and/or topped up with...

Senior Site Feasibility Specialist IQVIA BiotechLocation: PolandWork Model: HomebasedEmployment Type: Full-timeAbout the RoleIQVIA Biotech is seeking a Senior Site Feasibility Specialist to support our growing clinical operations this role you will lead country-level Site Activation (SA) activitie...

Work ScheduleOtherEnvironmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier cleaner and safer. We pro...

Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthrou...

Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthrou...