Warsaw, Masovian Voivodeship, Poland · On-site
As a CRA you will have local responsibility for the delivery of the studies at allocated sites and you will be an active participant in the local study team(s). You will work in close collaboration with other CRAs and th…
Skills: Clinical Monitoring, ICH-GCP, Site Management, Source Data Verification, Case Report Form Review
Warsaw, Masovian Voivodeship, Poland · Hybrid
$95k–$152k/yr
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less in…
Skills: Artwork Management, Regulatory Affairs, Labeling, Quality Check, Stakeholder Communication
Warsaw, Masovian Voivodeship, Poland · Remote OK
Job Overview The Medical Director for the Hematology-Oncology Center of Excellence provides strategic medical and scientific subject matter input to IQVIA in this therapeutic area informed by their training, experience a…
Skills: Oncology, Hematology, Clinical Development Planning, Protocol Design, Bid Defense
Warsaw, Masovian Voivodeship, Poland · Hybrid
$25k–$32k/mo
Do you get excited about the latest developments in ML & robot control? Are you ready to learn the new exciting world of smart robots? Do you strive in a fast paced and dynamic (startup) environment? Would you like to co…
Skills: Machine Learning, Deep Learning, Computer Vision, Python, Data Analysis
Warsaw, Masovian Voivodeship, Poland · On-site
$214k–$321k/yr
Location: Warsaw, Poland Job type: Permanent, full-time Field-based About the job As Medical Engagement Manager, Respiratory Poland within our Specialty Care Immunology CSE medical team, you'll implement the country medi…
Skills: Medical Affairs, KOL Relationship Management, Scientific Communication, Clinical Data Interpretation, Medical Strategy Development
Warsaw, Masovian Voivodeship, Poland · Remote OK
$13k–$26k/mo
Hi there!👋🏻We’re Tooploox 💎, a Solvd Inc. company We create AI-powered products and services that make a real difference. Our team of nearly 200 specialists - including a 40+ person R&D team with many PhDs - has pione…
Skills: Python, System Design, Database Management, REST API, LLM Orchestration
Warsaw, Masovian Voivodeship, Poland · Hybrid
📍 Financial Clinical Trial Assistant (CTA) – Hybrid | Warsaw We are looking for a dynamic and detail-oriented Financial CTA to join our client-dedicated (FSP) team in Warsaw. This role offers the opportunity to work in …
Skills: Excel, Payments Processing, Invoicing, Budget Support, Contract Management
Warsaw, Masovian Voivodeship, Poland · Hybrid
$294k–$356k/yr
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every …
Skills: Clinical Trial Operations, GCP, ICH Guidelines, Clinical Documentation, Stakeholder Management
Warsaw, Masovian Voivodeship, Poland · On-site
$321k–$471k/yr
CoreWeave is The Essential Cloud for AI™. Built for pioneers by pioneers, CoreWeave delivers a platform of technology, tools, and teams that enables innovators to build and scale AI with confidence. Trusted by leading AI…
Skills: Python, Go, Kubernetes, Distributed Systems, Inference Optimization
Warsaw, Masovian Voivodeship, Poland · On-site
$280k–$287k/yr
Minimum qualifications: Bachelor’s degree or equivalent practical experience. 2 years of experience with software development in one or more programming languages, or 1 year of experience with an advanced degree. 1 year …
Skills: Software Development, ML Infrastructure, GenAI, Large Language Models, Multi-Modal
Warsaw, Masovian Voivodeship, Poland · On-site
Tenstorrent is leading the industry on cutting-edge AI technology, revolutionizing performance expectations, ease of use, and cost efficiency. With AI redefining the computing paradigm, solutions must evolve to unify inn…
Skills: Machine Learning, PyTorch, TensorFlow, Python, C++
Warsaw, Masovian Voivodeship, Poland · Hybrid
Opis firmy Jako firma świadcząca usługi profesjonalne, Ayming współpracuje z firmami i instytucjami na całym świecie, aby sukcesywnie uwalniać ich potencjał. Nasz zespół skład się z ponad 1500 ekspertów ds. innowacji, HR…
Skills: R&D Tax Relief, IP Box, EU Grants, Project Management, Technical Analysis
Warsaw, Masovian Voivodeship, Poland · Hybrid
Opis firmy Jako firma świadcząca usługi profesjonalne, Ayming współpracuje z firmami i instytucjami na całym świecie, aby sukcesywnie uwalniać ich potencjał. Nasz zespół skład się z ponad 1500 ekspertów ds. innowacji, HR…
Skills: R&D Tax Relief, IP Box, EU Grants, Project Management, Business Relationship Management
Warsaw, Masovian Voivodeship, Poland · Remote OK
Company Description PrimeVigilance (part of Ergomed Group), is a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staf…
Skills: Pharmacovigilance, Regulatory Affairs, Project Management, ICH GCP, GVP
Warsaw, Masovian Voivodeship, Poland · On-site
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includ…
Skills: Device Preparation, Console Operation, Equipment Logistics, Clinical Study Procedures, Troubleshooting
Warsaw, Masovian Voivodeship, Poland · On-site
Requisition ID: 294815 Relocation Authorized: None Telework Type: Full-Time Office/Project Work Location: Warsaw Extraordinary teams building inspiring projects: Since 1898, we have helped customers complete more than 25…
Skills: Permitting Engineering, Air Dispersion Modeling, Environmental Impact Assessment, Regulatory Compliance, Technical Writing
Warsaw, Masovian Voivodeship, Poland · On-site
Teren: województwa Dolnośląskie, Lubuskie, Opolskie, preferowane miejsce zamieszkania: Wrocław i okolice KEY ACOUNT MANAGER odpowiada za wdrażanie i realizację strategii zarządzania kluczowymi klientami AstraZeneca w wyz…
Skills: Key Account Management, Strategic Planning, Relationship Building, Sales Analysis, Medical Communication
Sofia, Sofia-City, Bulgaria · Remote OK
Manager, Quality Assurance - Remote in Ireland, Poland or Bulgaria ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.…
Skills: Quality Assurance, Compliance, Audit Defense, People Leadership, Clinical Trial Management
Warsaw, Masovian Voivodeship, Poland · On-site
Teren: województwa Lubelskie, Świętokrzyskie, Podkarpackie, preferowane miejsce zamieszkania: Lublin, Rzeszów i okolice KEY ACOUNT MANAGER odpowiada za wdrażanie i realizację strategii zarządzania kluczowymi klientami As…
Skills: Key Account Management, Strategic Planning, Relationship Building, Sales Analysis, Medical Communication
Warsaw, Masovian Voivodeship, Poland · On-site
Teren: województwa Mazowieckie, Lubelskie; preferowane miejsce zamieszkania : Warszawa i okolice KEY ACOUNT MANAGER odpowiada za wdrażanie i realizację strategii zarządzania kluczowymi klientami AstraZeneca w wyznaczonym…
Skills: Key Account Management, Strategic Planning, Relationship Building, Sales Forecasting, Analytical Skills
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The CRA is responsible for the preparation, initiation, monitoring, and closure of clinical study sites to ensure compliance with international guidelines and local regulations. Key duties include performing source data verification, managing study supplies, and maintaining inspection-ready site files.
Candidates must have a minimum of 24 months of experience as a CRA and a bachelor's degree in a life science or related field. Proficiency in ICH-GCP guidelines and the ability to travel nationally and internationally are required.
As a CRA you will have local responsibility for the delivery of the studies at allocated sites and you will be an active participant in the local study team(s). You will work in close collaboration with other CRAs and the Local Study Team/ Local Study Manager to ensure that study commitments are achieved in a timely and efficient manner. You will act as the main contact with the study site and have the responsibility for monitoring the study conduct to ensure proper delivery of the study.
You will be responsible for the preparation, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with internal Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.
Contributes to the selection of potential investigators.
Trains, supports and advises Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principles.
Proves that site staff have completed and documented the required trainings appropriately, including ICH-GCP training, prior to and for the duration of the study. Ensures the sites are inspection ready at all times.
Initiates, monitors and closes study sites in compliance with AZ Procedural Documents. Shares information on patient recruitment and study site progress (site quality/performance) within the local study teams.
Drives performance at the sites. Proactively identifies and ensures timely resolution to study-related issues.
Updates CTMS and other systems with data from study sites as per required timelines.
Manages study supplies (ISF, etc), drug supplies and drug accountability at study site. Prepares study drug for destruction, if applicable.
Performs monitoring visits (remote and onsite), as well as remote data checks, in accordance with the timelines specified in the study specific Monitoring Plan. If required, determines and discusses with Local Study Manager (LSM) the correct timing and type of visits.
Performs Source Data Review (SDR), Case Report Form (CRF) review and Source Data Verification (SDV), in accordance with the Monitoring Plan.
Performs regular Site Quality Risk Assessments and adapts monitoring intensity accordingly during the study.
Ensures data query resolution in a timely manner.
Works with data management to ensure robust quality of the collected study data.
Ensures accurate and timely reporting of Serious Adverse Events and their follow ups.
Prepares and finalises monitoring visit reports in CTMS and provides timely feed-back to the Principal Investigator, including follow-up letter, within required timelines and in line with AZ SOP.
Follows up on outstanding actions with study sites to ensure resolution in a timely manner.
Follows quality issue processes by raising systematic or serious quality issues, data privacy breaches, CSP or ICH-GCP compliance issues to Local Management and/or CQM as required.
Assists site in maintaining inspection ready ISF.
Prepares for and collaborates with the activities associated with audits and regulatory inspections in liaison with LSM and CQM.
Ensures timely collection/uploading of crucial documents into the eTMF in accordance with ICH-GCP, AZ SOPs and local requirements. Supports/participates in regular QC checks performed by LSM or delegate.
Ensures that all study documents under their responsibility (i.e. site documents, relevant communications, etc) are available and ready for final archiving and completion of local part of the eTMF.
Ensures compliance with local, national and regional legislation, as applicable.
Bachelors degree in related subject area, preferably in life science, or equivalent qualification.
Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP, good knowledge of local regulations.
Good medical knowledge and ability to learn relevant AZ Therapeutic Areas.
Basic understanding of the drug development process.
Good understanding of Clinical Study Management including monitoring, study drug handling and data management.
Excellent attention to details.
Good written and verbal communication skills.
Good teamwork and interpersonal skills.
Ability to travel nationally/internationally as the need arises.
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
We're transforming the future of healthcare by unlocking the power of what science can do for people, society and the planet. For more information, visit www.astrazeneca.com. Community Guidelines: bit.ly/2MgAcio
Offices: 1 Francis Crick Avenue, Cambridge Biomedical Campus, Cambridge, Cambridgeshire CB2 0AA, GB · Astraallen, Sodertalje, Stockholm County 152 57, SE
There are currently 169 open science & research positions in Warsaw, Poland listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include AstraZeneca, ICON plc, IQVIA, Bristol Myers Squibb, Fortrea, among others. Browse the listings above to see every active employer.
Yes — 106 of the 169 open science & research positions offer remote or hybrid work (39 remote, 67 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
