Lavori attuali relativi a Clinical Project Lead - Turbigo MI - Barrington James
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Clinical Project Lead
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Turbigo, Italia Barrington James A tempo pienoClinical Project Manager – Neuro / Psychiatry Location Department Clinical Operations Reports to Senior Clinical Project Manager / Director of Clinical Operations Job Purpose The Clinical Project Manager (CPM) is responsible for the planning, execution, and delivery of clinical trials within Neurology and Psychiatry, ensuring studies are conducted on time,...
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Clinical Project Lead
1 settimana fa
Turbigo, Italia Barrington James A tempo pienoClinical Project Manager – Neuro / PsychiatryLocationDepartmentClinical OperationsReports toSenior Clinical Project Manager / Director of Clinical OperationsJob PurposeThe Clinical Project Manager (CPM) is responsible for the planning, execution, and delivery of clinical trials within Neurology and Psychiatry, ensuring studies are conducted on time, within...
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Neuro & Psychiatry Clinical Trial Lead
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Turbigo (MI), Italia Barrington James A tempo pienoA leading clinical research organization is seeking a Clinical Project Manager to oversee clinical trials in Neurology and Psychiatry. The ideal candidate will lead cross-functional teams, manage timelines and budgets, and ensure compliance with regulations. Applicants should have a Bachelor's degree in Life Sciences and experience with clinical trials in...
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Clinical Project Lead: End-to-End Study Delivery
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Turbigo, Italia IQVIA A tempo pienoA leading clinical research organization is looking for a Project Lead located in Turbigo, Italy. This role involves managing the delivery of clinical studies, collaborating with various teams and stakeholders, and ensuring compliance with regulatory requirements. Applicants should possess a Bachelor's degree in Life Sciences, have at least 5 years of...
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Local Clinical Project Management Sponsor Dedicated
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Local Clinical Project Management Sponsor Dedicated
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Turbigo, Italia IQVIA A tempo pienoJob Overview Project Leads are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs policies...
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Senior Data Management Lead
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Turbigo, Italia PSI CRO A tempo pienoA leading clinical research organization in Turbigo, Italy, seeks a Lead Data Manager to manage project data communication between teams and clients. The role requires a college or university degree, a minimum of five years of CRO industry experience, and proficiency in CDM/EDC systems such as Medidata Rave or Oracle Inform. Strong communication and...
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Gastroenterology Medical Monitor: Clinical Trials Lead
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Turbigo (MI), Italia Altro A tempo pienoA leading Contract Research Organization in Italy is seeking a Medical Monitor to provide medical input to clinical studies and ensure patient safety. The role involves advising project teams and regulatory agencies, reviewing clinical data, and leading safety monitoring boards. Candidates must possess a Gastroenterology Fellowship certification, have a...
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Clinical Research Associate
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Turbigo (MI), Italia PHIDEALIVE Srl A tempo pienoCompany Description Phidealive, established in 2018, is a Contract Research Organization (CRO) with a strong foundation in Italy's rich clinical research culture. Positioned as a Clinical Research Atelier, Phidealive emphasizes scientific rigor, regulatory compliance, and a tailored operational approach for each project. The company collaborates with Pharma,...
Clinical Project Lead
53 minuti fa
Clinical Project Manager – Neuro / Psychiatry Location Department Clinical Operations Reports to Senior Clinical Project Manager / Director of Clinical Operations Job Purpose The Clinical Project Manager (CPM) is responsible for the planning, execution, and delivery of clinical trials within Neurology and Psychiatry, ensuring studies are conducted on time, within budget, and in compliance with ICH‐GCP, EU regulations, and company SOPs. The CPM will lead cross‐functional teams and act as the primary operational contact for sponsors, CRO partners, and internal stakeholders. Key Responsibilities Clinical Trial Management Lead the operational management of Phase I–IV clinical trials in Neurology and/or Psychiatry Develop and maintain project plans, timelines, budgets, and risk mitigation strategies Ensure trial delivery meets quality, timeline, and financial objectives Oversee study start‐up, site activation, enrolment, monitoring, and close‐out activities Cross‐Functional Leadership Coordinate internal teams including Clinical Operations, Data Management, Biostatistics, Pharmacovigilance, and Regulatory Affairs Manage external vendors, CROs, central laboratories, and imaging providers Chair study team meetings and ensure clear communication across all stakeholders Support site selection, feasibility assessments, and investigator engagement Monitor site performance, enrolment, and protocol compliance Address operational challenges related to Neuro/Psych populations (e.g. recruitment, retention, patient burden) Regulatory & Quality Compliance Ensure trials comply with ICH‐GCP, EU Clinical Trial Regulation (CTR), GDPR, and local Italian regulatory requirements Support submissions to Ethics Committees and Competent Authorities Ensure inspection and audit readiness throughout the study lifecycle Budget & Financial Management Develop and manage study budgets and forecasts Track study spend and manage change orders Ensure timely investigator payments and vendor invoicing Identify operational risks early and implement mitigation strategies Escalate issues appropriately and provide clear solutions to stakeholders Lead corrective and preventive actions (CAPAs) when required Therapeutic Area Focus – Neuro / Psychiatry Manage trials involving CNS indications such as neurological disorders, psychiatric conditions, or neurodevelopmental diseases Oversee complex assessments (e.g. rating scales, cognitive testing, imaging, digital endpoints) Ensure patient‐centric approaches for vulnerable populations and long‐term studies Person Specification Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related discipline Proven experience as a Clinical Project Manager or Senior Clinical Trial Manager Strong experience managing Neurology and/or Psychiatry clinical trials In‐depth knowledge of ICH‐GCP and EU clinical trial regulations Demonstrated ability to manage multiple studies and cross‐functional teams Excellent communication, leadership, and organisational skills Fluency in English (written and spoken) Experience working in Italy and familiarity with AIFA and Ethics Committee processes CRO and/or sponsor‐side experience Experience with decentralised or hybrid trial designs Master's degree or project management certification (e.g. PMP, PRINCE2) Fluency in Italian What We Offer Opportunity to work on innovative CNS clinical trials International and collaborative working environment Competitive salary and benefits package Professional development and career progression opportunities #J-18808-Ljbffr