Clinical Research Associate
2 giorni fa
Our client is a leading company in the Pharma Sector.We are seeking a Senior Clinical Research Associate to join our teamYou new roleEnsure compliance with client SOPs, study protocols, ICH-GCP and applicable regulationsTrain and support investigator site teams on study procedures and systemsConduct site initiation, monitoring (on-site and remote), and close‑out visitsVerify informed consent, study material management, and biological sample handling (if applicable)Monitor data accuracy and quality by verifying eCRF data against source documentsReview and ensure proper reporting of adverse events (AEs/SAEs)Maintain investigator site files and manage essential regulatory documentationPrepare visit reports and follow up on action items with site teamsProvide technical support for eCRF systems and data entryMaintain regular communication with investigators and project teamsSupport patient recruitment and investigator engagementManage study archiving and support site billing processesYou will be involved in the IRB submission process (for linguistic support).RequirementsRequired experience level: Ideally experience in ATTR cardiac amyloidosis and in non‑interventional studies. If this is not possible, we search for a confirmed/senior CRA.At least 10 years experience in the role and functions describe above.The HQ is based in Italy in Florence.What to do nowIf you are interested in this opportunity, click on \"Apply now\". If this opportunity is not in line with your expectations, but you are looking for a new job, visit our website to discover new ones.Candidates of both sexes, after having read the mandatory privacy information on the website are asked to send their CV. Hays Solutions S.r.l. with sole shareholder. Subject to the direction and coordination of Hays Plc#J-18808-Ljbffr
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Clinical Research Associate
7 giorni fa
Firenze, Italia Translational Research in Oncology A tempo pienoA global clinical research organization is seeking an experienced Clinical Research Associate to join their Monitoring Resources team. The role involves conducting site visits, ensuring compliance with regulations, and mentoring junior staff. Candidates should have at least 2 years of oncology trial monitoring experience, be fluent in English, and hold a...
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Clinical Research Associate
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Firenze, Italia Translational Research in Oncology A tempo pienoIf you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you! Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is...
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Clinical Research Associate
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Firenze, Italia Translational Oncology Research, LLC A tempo pienoIf you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you! Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is...
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Oncology Clinical Research Associate
2 giorni fa
firenze, Italia Translational Oncology Research, LLC A tempo pienoA global clinical research organization is seeking an experienced Clinical Research Associate to join its Monitoring Resources team. The role involves conducting site visits, ensuring adherence to FDA and ICH-GCP guidelines, and mentoring junior team members. Candidates should have a minimum of 2 years of experience in oncology trials and a Bachelor's degree...
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Oncology Clinical Research Associate
4 giorni fa
firenze, Italia Translational Oncology Research, LLC A tempo pienoA global clinical research organization is seeking an experienced Clinical Research Associate to join its Monitoring Resources team. The role involves conducting site visits, ensuring adherence to FDA and ICH-GCP guidelines, and mentoring junior team members. Candidates should have a minimum of 2 years of experience in oncology trials and a Bachelor's degree...
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Remote Oncology Clinical Research Associate
7 giorni fa
Firenze, Italia Translational Research in Oncology A tempo pienoA global clinical research organization is seeking an experienced Clinical Research Associate to join their Monitoring Resources team. The role involves conducting site visits, ensuring compliance with regulations, and mentoring junior staff. Candidates should have at least 2 years of oncology trial monitoring experience, be fluent in English, and hold a...
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Senior Clinical Research Associate
2 giorni fa
firenze, Italia JR Italy A tempo pienoOverviewPOSITION SUMMARY: The Senior Clinical Research Associate (Senior CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with applicable regulatory standards (MDR, ISO 14155, ICH/GCP guidelines, Teleflex procedures and IRB/EC policies and procedures). The Senior CRA conducts monitoring visits as identified...
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Senior Clinical Research Associate
4 ore fa
Firenze, Italia Jr Italy A tempo pienoOverviewPOSITION SUMMARY: The Senior Clinical Research Associate (Senior CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with applicable regulatory standards (MDR, ISO *****, ICH/GCP guidelines, Teleflex procedures and IRB/EC policies and procedures).The Senior CRA conducts monitoring visits as identified...
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Firenze, Italia Jr Italy A tempo pienoA leading medical device company in Tuscany is seeking a Senior Clinical Research Associate to conduct monitoring visits and ensure compliance with regulatory standards.The ideal candidate will have at least 5 years of clinical trial monitoring experience, strong communication skills, and the ability to work independently.Proficiency in both Italian and...
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Senior Clinical Research Monitor — On-Site
4 giorni fa
firenze, Italia JR Italy A tempo pienoA leading medical device company in Tuscany is seeking a Senior Clinical Research Associate to conduct monitoring visits and ensure compliance with regulatory standards. The ideal candidate will have at least 5 years of clinical trial monitoring experience, strong communication skills, and the ability to work independently. Proficiency in both Italian and...
