Medical Products Jobs in Poland

opracowywanie mapy drogowej dla grupy produktowej InfoSec i zarzdzanie ni w tym identyfikowanie nowych moliwoci produktowych i okrelanie ich wykonalnocizarzdzanie procesem rozwoju produktu w tym zbieranie wymaga projektowanie produktu testowanie i wprowadzanie na rynekprzeprowadzanie More...

Job DescriptionThe Medical Reviewer II is responsible for medical review of lCSRs and literature review writing signal detection reports supporting writing and or reviewing of aggregate reports (DSURS PSURS/PBRERs/PADERS) as required by the Company or Client.For the Client:To review a More...

Therapeutic area: OncologyTerritorial scope (districts): lskie maopolskie witokrzyskie podkarpackie lubelskie.The Medical Science Liaison (MSL) is a nonpromotional field based scientific expert in a given therapeutic area(s) that strategically supports the medical and scientific objec More...

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and wellbeing.Hybrid work in WarsawResponsibilities:Medical point of contact for internal project team study sites and st More...

The Medical Reviewer I is responsible for medical review of lCSRs and literature review writing of signal detection reports supporting writing and or reviewing of aggregate reports (DSURS PSURS/PBRERs/PADERS) as required by the Company or Client. Responsibilities include:To revie More...

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and wellbeing.Hybrid work in WarsawResponsibilities:Medical point of contact for internal project team study sites and st More...

Responsibilities include:To review and approve postmarketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness listedness / expectedness and Com More...

For the Client:To review and approve postmarketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. The review includes coding seriousness assessment Company causality and comment listedness/e More...

International and country level medical engagement projects management (internal and external scientific events HCPs logistics management scientific communication projects).Support and lead defined stages in the defined geographies Medical Programs management: Managed Access (compassi More...

PrimeVigilance is looking for a Medical Information Associate to be responsible for supporting the Medical Information team in handling initial adverse event and medical information inquiries in Polish and English.  Responsibilities  To provide approved responses to med More...

Location: Germany (Various Locations)We are seeking medical doctors specializing in internal medicine (m/f/d) with proficiency in German (at least B2/C1 level) to join leading German hospitals and occupational health centers. This opportunity is open to candidates within the EU and ou More...

We currently have an exciting opportunity at SGS for a Medical Devices Lead Auditor & Training Specialist to join our highly successful Global Medical Device team.In this role you will be reporting directly to the Global Medical Devices Technical Training Manager.Your role wi More...

The PrimeVigilance Senior Medical Writer position offers a unique opportunity to further develop your career in the field of drug safety.Key ResponsibilitiesIndependent authoring editing and reviewing of various regulatory/clinical documents (e.g. aggregate reports risk managemen More...

The PrimeVigilance Senior Medical Writer position offers a unique opportunity to further develop your career in the field of drug safety.Key ResponsibilitiesIndependent authoring editing and reviewing of various regulatory/clinical documents (e.g. aggregate reports risk managemen More...

The Senior Pharmacovigilance (PV) Physician II is responsible for medical review of ICSRs writing and reviewing signal detection reports writing and/or reviewing aggregate reports (DSURS PSURS/PBRERs/PADERS ACOs responses to regulatory authority requests) writing and/or reviewing risk More...

The Senior Pharmacovigilance (PV) Physician I is responsible for medical review of ICSRs writing and/or reviewing signal detection reports writing and or reviewing aggregate reports (DSURS PSURS PBRERs. PADERS) reviewing risk management reports (RMPs) and mentoring junior PV Phys More...

As a Product Assessor you will be responsible for conducting comprehensive assessments of Cardiovascular and Soft Tissue products ensuring technical file reviews adhere to all applicable requirements including the European Medical Device Regulation (MDR) Medical Device Directive (MDD) More...

In this role you will:Act as the main line of communication between the Sponsor or CRO and the site.Ensure response to feasibility questions are provided in due time.Assist in scheduling and preparation for all types of monitoring visits at the medical institution/resea More...

Milestone One Site Coordinator supports trial sites in all related activities according to ICHGCP protocol requirements within Study specific defined timelines and enrollment goals.In this role you will:Act as the main line of communication between the Sponsor or CRO and the site More...

Location: Warsaw Poland Work model: Onsite Employment type: Fulltime Remuneration: Base salary bonuses DUTIES AND RESPONSIBILITIES: Make engaging outbound calls daily to connect with both current and potential players.Assist new and existing players to enhance their experience and More...