Experienced Clinical Research Associate, IQVIA Biotech
2 settimane fa
Experienced Clinical Research Associate, IQVIA Biotech - Home based, Italy Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Responsibilities Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability. Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. Collaborate and liaise with study team members for project execution support as appropriate. If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications University Bachelor\'s Degree and Master\'s Degree in scientific discipline or health care In possession of CRA Certification as required by Ministerial Decree dated Experience in Pharma Industry, and/or Clinical Trials environment Very good computer skills including MS Office Excellent command of English language Organizational, time management and problem-solving skills Ability to establish and maintain effective working relationships with coworkers, managers, and clients Flexibility to travel Driver's license class B #J-18808-Ljbffr
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Experienced Clinical Research Associate, IQVIA Biotech
4 settimane fa
WorkFromHome, Italia IQVIA LLC A tempo pienoExperienced Clinical Research Associate, IQVIA Biotech - Home based, Italy page is loaded## Experienced Clinical Research Associate, IQVIA Biotech - Home based, Italylocations: Milan, Italytime type: Full timeposted on: Posted Todayjob requisition id: R Job Overview:Perform monitoring and site management work to ensure that sites are conducting the...
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Experienced Clinical Research Associate, IQVIA Biotech
2 settimane fa
WorkFromHome, Italia IQVIA A tempo pienoExperienced Clinical Research Associate, IQVIA Biotech - Home based, Italy 1 day ago Be among the first 25 applicants Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential...
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Experienced Clinical Research Associate, IQVIA Biotech
3 settimane fa
WorkFromHome, Italia IQVIA A tempo pienoExperienced Clinical Research Associate, IQVIA Biotech - Home based, Italy Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Responsibilities Perform site monitoring visits...
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Senior Remote CRA – Home-Based in Italy
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WorkFromHome, Italia IQVIA A tempo pienoA leading biotech company is seeking an Experienced Clinical Research Associate to perform monitoring and site management work. Responsibilities include site visits, quality assessment, and regulatory compliance. Candidates should have a Bachelor’s and Master’s degree in a scientific discipline or health care, CRA certification, and experience in the...
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Clinical Research Associate
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WorkFromHome, Italia Philogen S.P.A. A tempo pienoPhilogen S.p.A., a biotech company listed on the Milan Stock Exchange and a leader in the development of innovative anti-tumor therapies, is expanding its clinical activities and will be opening a new office in Milan. Philogen S.p.A. would like to hire a CLINICAL RESEARCH ASSOCIATE for the development of clinical experimental activity. The successful...
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WorkFromHome, Italia Whatjobs A tempo pienoJoin to apply for the Senior CRA role at Thermo Fisher Scientific 1 day ago Be among the first 25 applicants Join to apply for the Senior CRA role at Thermo Fisher Scientific Work Schedule Other Environmental Conditions Office At PPD, part of Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our...
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WorkFromHome, Italia ICON A tempo pienoClinical Research Associate ( CRA II or Senior CRA) - Romania - Hybrid ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking...
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WorkFromHome, Italia IQVIA A tempo pienoA leading global provider of clinical research services is seeking an Experienced Clinical Research Associate to monitor and manage clinical study sites based in Italy. The ideal candidate will have a Bachelor's degree and a Master's degree in a scientific field or health care, along with CRA certification. The role involves ensuring regulatory compliance,...
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Integrated Research
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WorkFromHome, Italia IQVIA A tempo pienoJoin to apply for the Integrated Research - Senior Principal role at IQVIA . Location: EU-Wide (hybrid/remote) Real World Commercial Solutions to Create a Healthier World In RWCS we’re passionate about improving the life sciences ecosystem and making decisions that accelerate innovation for a healthier world. Every day our team develops evidence-based...
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Senior Clinical Research Associate
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WorkFromHome, Italia Experteer Italy A tempo pienoA leading clinical research organization is seeking a Clinical Research Associate in Italy, focusing on site monitoring for clinical trials. The role includes overseeing compliance and collaborating with the Clinical Monitoring team. Ideal candidates will have a Bachelor’s degree in a scientific health field and possess strong organizational and...
