Aktualne oferty pracy związane z Clinical Team Lead II Professional - Warszawa, Mazovia - TN Poland
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Country Clinical Lead
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Clinical Research Professional
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Clinical Support Professional
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Clinical Research Professional
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Clinical Research Associate Professional
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International Clinical Trials Manager
6 dni temu
Warszawa, Mazovia, Polska Rho, Inc. Pełny etatJob DescriptionRho, Inc. is a leading Contract Research Organization (CRO) with a global presence.We are seeking a highly experienced Freelance Clinical Project Manager to join our team in the EU, working on a freelance basis to manage international Phase I-IV clinical trials.Main DutiesManage clinical studies from start to finish, ensuring compliance with...
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Clinical Trial Manager II, Dermatology
4 tygodni temu
Warszawa, Mazovia, Polska TN Poland Pełny etatClinical Trial Manager II, Dermatology & RheumatologyJob Summary:The Clinical Trial Manager II (CTM II) is responsible for the operational management and oversight of clinical investigative sites as well as clinical monitoring deliverables of clinical trials.Responsibilities:Ensures timely quality deliverables and in accordance with applicable standard...
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Senior Clinical Project Manager, Remote, EU
4 tygodni temu
Warszawa, Mazovia, Polska Rho, Inc. Pełny etatJob OverviewWe are seeking a Senior Clinical Project Manager to join our team at Rho, where we take healthcare and clinical research personally. Our shared experiences drive a passion to heal, cure, and solve humanity's biggest challenges.You will have the opportunity to experience a thriving company with real stability - financial, workforce, and corporate,...
Clinical Team Lead II Professional
1 tydzień temu
Rho is redefining the CRO experience. We take healthcare and clinical research personally, with shared experiences driving a passion to heal, cure, and solve humanity's biggest challenges.
We're committed to our employees, providing a stable environment to innovate and develop over a long and rewarding career. Our collaborative team of smart, talented, and positive individuals celebrates and respects expertise, offering freedom to think creatively, challenge the norm, and problem-solve.
Key Responsibilities:
- Drive project success by working closely with Project Managers to develop and implement enrollment strategies.
- Manage operational aspects of planning and site performance in accordance with departmental productivity expectations.
- Develop monitoring tools and plans to ensure sites operate in compliance with study protocols and ICH/GCP guidelines.
- Lead regular clinical team teleconferences and work effectively with Site Study Coordinators.
- Participate in RFP processes and review monitoring visit reports to ensure finalization within contractual timelines.
Requirements:
- 8+ years of clinical research experience, including 2 years leading clinical operations functions and at least 2 years of on-site monitoring experience.
- BA/BS in a life science, nursing, pharmacy, or related field.
- Demonstrated understanding of medical/therapeutic area knowledge and medical terminology.
- Strong communication skills to showcase successes and promote quality.