Clinical Research Associate Sponsor Dedicated - CZ… - Jobeax
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Clinical Research Associate Sponsor Dedicated - CZ Republic v Brandýs nad Labem-Stará Boleslav, Česko
Plný úvazekStandardní týdenní pracovní doba
Czech Republic, Brandýs nad Labem-Stará Boleslav
Clinical Research Associate Sponsor Dedicated - CZ Republic v Brandýs nad Labem-Stará Boleslav, Česko is listed on Jobeax. Browse 80,000+ vacancies available.
Clinical Research Associate Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices in accordance...
Plný úvazek
Pružná doba
... drive industry leading performance. Partners with the investigator and site staff for meaningful and effective engagements positioning AbbVie as the choice in clinical trials. Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study ...
... drive industry leading performance. Partners with the investigator and site staff for meaningful and effective engagements positioning AbbVie as the choice in clinical trials. Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study ...
... license in good standing, with unrestricted ability to practice in place of work, where applicable - A valid ICH GCP certificate - No previous experience in clinical research years of required, but must have general medical practitioner diagnosis and treatment proficiency In some cases an equivalency, consisting of a combination ...
... Pharmacy, Nursing, or a related field. - Experience in clinical research, clinical operations, monitoring, or risk-based monitoring. - Strong understanding of clinical trial processes, GCP, and regulatory requirements. - Experience working with clinical trial data and performance metrics. - Knowledge of Key Risk Indicators ...
... svátek. - Umíš plynule česky slovem i písmem (B2/C1). - Máš základy angličtiny (pro navigaci v našich systémech). Na co se můžeš těšit: - Počáteční mzdu 140 - 150 CZK / hodina (dle zkušeností). - Možnost rychlého růstu na pozici vedoucího směny (v řádu týdnů/měsíců) a s ním spojené vyšší platové ohodnocení. - Smlouvu na částečný ...
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JOB DESCRIPTION Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Supports compliance to the clinical trial process by ensuring all study documentation and source data is captured accurately in eCRF, up to date and first time right. Performs quality review and answers any eCRF queries for ...
... technologies - Vendor management skills - Experience in the pharmaceutical industry - Experience with GxP validations, particularly in GCP (Good Clinical Practices) - Clinical data standards – CDISC SDTM, ADaM - Experience working in a product team - Databricks, PySpark, Terraform Why Join Us? - Join a team dedicated to saving and ...
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... Praha 7, a to pouze po předchozí domluvě. Zaměstnanecké výhody: Zaměstnanecké slevy na firemní produkty, příspěvky na stravování, cafeterie Společnost https://jobeax.com/link/SB1o4cE6MLQLCTfF a.s. hledá vhodného kandidáta na pozici Warehouse associate- junior (m/ž).
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