Praca Cra cta Warszawa

 ...shape the future of mRNA medicines. Based in Warsaw as an individual contributor, you will lead worldwide Clinical Trial Application (CTA) operations outside the United States, excluding US Investigational New Drug (IND) submissions. You will provide operational and... 

Fortrea seeks Clinical Research Associates for anticipated upcoming opportunities in clinical trial monitoring. The role involves managing study sites, conducting monitoring visits, ensuring data integrity, and maintaining regulatory compliance across clinical trials in...

 ...Senior CRA, home based, Poland, late phase clinical trials ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration... 

 ...onboarding, training, and knowledge sharing across the team.  ~ Serve as a subject matter expert for clinical trial processes and may lead CTA study teams and contribute to recruitment activities.  ~ Support departmental quality and process improvement initiatives... 

 ...POL-HB- Sr CTA At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment... 

Senior Clinical Research Associate role at ICON based in Warsaw, Poland, responsible for overseeing clinical trial monitoring activities across multiple sites. The position requires extensive experience in clinical trial processes, regulatory compliance, and site management...

Medical Writer Miejsce pracy: Warszawa Your responsibilities Collect, appraise and analyze clinical data pertaining to a medical device. Write documentation, such as Clinical Evaluation Reports (CERs) and Post-Market Clinical Follow-Up (PMCF) Reports, supporting...

 ...POL-CTA-JJ At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment... 

 ...Associate position at ICON in Warsaw supporting sponsor-dedicated clinical trial management. Requires Bachelor's degree and 2-3 years of CTA experience in pharmaceutical or CRO settings to handle documentation, regulatory submissions, site coordination, and cross-functional... 

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 includes full service-capabilities, resourcing and Functional...

JOB DESCRIPTION Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description The Internship Program is focused on motivating, engaging and developing outstanding new graduates to support the continued success of the business showing...

 ...regional/country requirements. • Payment request is performed on time and accurately according to the agreed frequency as outlined in the CTA. • For all payments, track communications and approvals in the appropriate systems. • Ensure payment metrics and required actions... 

Labcorp seeks a remote Investigator Support Assistant in Warsaw on a 2-year contract to manage clinical trial communications, track laboratory results, and support research sites and sponsors. The role requires fluency in English and Italian, with a flexible schedule including...

About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic...

AstraZeneca seeks an analyst to process and anonymize clinical study documents for regulatory submissions and data sharing initiatives. The role supports global compliance with Health Canada PRCI, EMA policies, and clinical trial transparency requirements, working with...

Are you a passionate Life Sciences student looking to gain hands-on experience in the fast-paced world of clinical trials? We are partnering with an innovative biotechnology company dedicated to developing groundbreaking, high-impact therapies for patients with severe ...

Clinical Independent Rater - Polish Speaking Location: Remote/Virtual Hours: Estimated 10–16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated...

 ...trials, ensuring protocol compliance, and managing data integrity across sponsor-dedicated projects. Requires Bachelor's degree, 2+ years CRA experience, and willingness to travel approximately 40%. Responsibilities Conduct site qualification, initiation, monitoring,... 

 ...English language ~ Location: central-northern Poland (Warsaw, Poznań, Łódź area) ​#weareIQVIA #projectpatientfocus #LI-Remote #CRA IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences... 

Clinical Functional Service Partnership role supporting dedicated pharmaceutical or biotechnology sponsor programs. Candidates will manage trial documentation, coordinate study supplies, and support clinical operations while developing expertise within a global clinical...

 ...collaborating with leading pharma companies to help patients all around the world? When you join IQVIA as a sponsor-dedicated Senior CRA in Poland, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience... 

Medical Advisor / Medical Trainer – medycyna estetyczna Miejsce pracy: Warszawa Twój zakres obowiązków opracowywanie programów i treści merytorycznych szkoleń produktowych oraz eksperckich skierowanych do lekarzy medycyny estetycznej, dermatologów i lekarzy innych...

A 12-month career starter program in medical affairs for the cardiovascular/respiratory therapeutic area. Trainees will support medical affairs projects, including literature analysis, medical writing, and educational materials development under mentor guidance. Responsibilities...

Entry Level Project Associate. 3 days in either or Warsaw or Sofia office and 3 days working from home ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values...

Clinical Trial Associate position supporting sponsor-dedicated clinical research operations. The role involves coordinating trial administration, managing documentation, and collaborating across teams to ensure regulatory compliance and successful trial execution in a ...

JOB DESCRIPTION Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission...

JR152781 Project Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are...

Fortrea seeks a motivated intern to support clinical trial start-up and site management activities in Warsaw. The 12-month position offers hands-on exposure to the clinical trial lifecycle, including feasibility assessment, site activation, documentation management, and...

Specjalista Kliniczny / Specjalistka Kliniczna ds. Wyrobów Medycznych Miejsce pracy: Warszawa Twój zakres obowiązków prowadzenie szkoleń dla pielęgniarek i personelu medycznego z zakresu użytkowania wyrobów medycznych firmy Margomed na terenie całej Polski ...

ICON seeks a Site Engagement Liaison to build and maintain relationships with clinical trial sites across Poland. The role involves supporting site staff on protocols and regulatory requirements, identifying performance improvements, and collaborating with internal teams...