Rezultatul căutării: 20 oferte de muncă active
...relationships
precision
make strategic business decisions
We have current opportunity for an experienced Clinical Trial Manager in Europe! Join our growing team.
Precision for Medicine is a precision medicine CRO. Precision's uniquely integrated...
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...globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic,... ...and staff.
Protect patients. Review the performance of the trial at designated sites, ensure the rights and well-being of human...
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...Description
Senior Clinical Research Associate I
Syneos Health® is a leading fully integrated biopharmaceutical solutions... ...and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is aware...
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...about our employee referral program
The Job's Mission
The Clinical Support Specialist responsibilities include directly supporting... ...offer our customers the best possible solution
Conducting trials and evaluations of product in theatre and clinical environment...
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...Description
Clinical Quality Assurance Manager (QA Manager)
Romania / Bucharest
Hybrid Location... ...of multiple audit types (e.g. vendors, investigator sites, trial master files, data management, safety reporting, and laboratories...
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...Chloe O'Shea is looking for a Clinical Research Associate II to join her clients global leading CRO. You will be working on multiple therapeutic... ...Participate in the development and review of clinical trial-related documents
Ensure that trial sites are adequately trained...
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...Who we are
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with... ...applicable updates for site related documentation for filing in the Trial Master File (TMF)
Perform feasibility studies/site...
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...Who we are
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with... ...payments to investigative sites are aligned with the Clinical Trial Agreement, perform payment reconciliations at mandated intervals...
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...treatment (palliative radiation and curative breast radiation).
General palliative treatment for most tumour types.
Participation in clinical trials and research.
Training and guidance of resident doctors.
Qualifications:
European authorisation as a medical professional....
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...Description
Responsibilities:
Inspect near-real-time aggregate clinical and operational data from multiple sources (eCRF, vendor data,... ...ICH/GCP guidelines as they relate to the conduct of clinical trials (study management, data management and regulatory operations)....
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...accelerate customer success. We translate unique clinical, medical affairs and commercial insights... ...statistical analysis results of clinical trials on behalf of the sponsor.
• Manages... ...Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your...
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...integrity come together to advance the state of clinical development.
As a Senior/Principal... ...or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote... ..., analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE),...
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...We are currently looking for experienced Project Quality and Risk Leads with expertise with ICH-GxP principles and clinical trial regulations to be based in Romania or Poland or Lithuania or Hungary.
As the Senior Project Quality and Risk Lead you will actively...
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...organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical,... ...You will be responsible for execution and oversight of clinical trial country submissions and approvals and to enure Site Ready....
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...countries around the world. We support pharmaceutical, biotechnology, and medical device companies with the services needed to perform clinical trials of new medicines. Our work helps patients in need improve their well-being – a fundamental driver for many of us to show up and...
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...organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical,... ...consistent approach to the review of safety data emerging from clinical trials and from the post-marketing environment.
Chairs the Safety...
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...therapy area and provide internal medical guidance. Contribute to clinical development and life cycle management of Novartis portfolio, in... ...Programs (MAP), Investigator-Initiated research studies and Trials (IITs) and Research Collaborations (RC)
• Build and execute TA...
...responsibilities
Inspect near-real-time aggregate clinical and operational data from multiple... ...they relate to the conduct of clinical trials (study management, data management and... ...and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
#LI-KU1...
...organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to... ...individual studies based on the requirements of the clinical trial.
• Assists in administration of contract management and essential...
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...organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical,... ...thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development...
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