Lavoro Clinical Trial Manager Parma

Select how often (in days) to receive an alert:Clinical Trial Documentation & Records Management LeadDepartment: Global Clinical DevelopmentBusiness Area: R&D, Pharmacovigilance & Regulatory AffairsJob Type: Direct EmployeeContract Type: PermanentLocation: Parma, ITAbout usBased in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with 90 years’...

A leading pharmaceutical company is seeking a Clinical Trial Documentation & Records Management Lead in Parma, Italy. This role involves establishing and improving the documentation unit, ensuring compliance with regulatory standards. Ideal candidates will have 8-10 years of clinical operations experience, strong leadership skills, and knowledge of eTMF and CTMS systems. Flexible hybrid working...

Who we are looking for This is what you will do The Clinical Trial Documentation Records Management Lead is responsible for establishing, leading, and continuously improving the Clinical Trial Documentation Records Management Unit within Chiesi GCD. This role ensures alignment between organizational and technical requirements for clinical trial documentation and records, driving the adoption and...

On behalf of our Client - Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world, with more than 80 years of experience within the pharmaceutical and biotechnology industry a global pharmaceutical company - IQVIA is looking for a eTMF Specialist who can join an exciting working environment in a dynamic atmosphere. This position will oversee the global eTMF (electronic Trial...

The Clinical Education Manager Ultrasonics & Consumables is part of the Clinical Education Team. Reporting to the Head of Training & Clinical Education, He/She is responsible for: Leading the Clinical Education & Marketing strategy for Acteon Ultrasonics & Consumables solutions in line with downstream Marketing, with R&D, Regions to switch from technical argumentation to clinical argumentation,...

Farmapiù, divisione specialistica di Lavoropiù, seleziona un/una Clinical Education Manager che si occuperà della linea di prodotti Ultrasonics & Consumables per azienda multinazionale operante nel settore dentale/medicale a livello nazionale e internazionale. Sede di Lavoro: Full Remote + Trasferte al 80% del tempo (Estero e Italia) Requisiti: Laurea triennale oppure Magistrale in Ingegneria...

IQM Selezione cerca, per una azienda con sede a Novara (NO) specializzata in data management, all'avanguardia e attiva a livello internazionale, un/una: Clinical Data Manager La risorsa selezionata si occuperà di: Pianificazione: • Analisi del protocollo e definizione del piano di Data Management (DMP). • Pianificazione CDISC e sviluppo del flusso dati (SDFD). Sviluppo e Validazione Database: •...

Social network you want to login/join with: Senior Clinical Research Associate, parma col-narrow-left Client: Teleflex Location: Job Category: Other - EU work permit required: Yes col-narrow-right Job Reference: 8556790222002585600337114 Job Views: 2 Posted: 27.08.2025 Expiry Date: 11.10.2025 col-wide Job Description: POSITION SUMMARY: The Senior Clinical Research Associate...

POSITION 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 by the monitoring plan, study team or...

Veeda Lifesciences is seeking a Clinical Research Associate (CRA) based in Italy for its growing international hematology/oncology Clinical Trials program. This is a full-time job. Job overview: The CRA is responsible for ensuring that the conduct of a clinical trial at selected Investigational Sites is according to the currently approved protocol/amendments, ICH GCP guidelines, the applicable...

Senior Clinical Research Associate (Oncology) Working embedded with a leading global oncology-focused biopharmaceutical company We are partnering with a top-tier global biopharmaceutical organisation to support a growing oncology portfolio and are seeking an experienced Clinical Research Associate to join the team in an advanced, hands-on clinical role. This position offers the opportunity to...

Purpose To manage the administrative and documentation aspects of clinical trials at every stage of the process (study documentation, maintaining databases, creating/ updating trackers and support with supplies management) Main Responsibilities Support the CPM in preparation of study TMF Plan and Map, and other Clinical Study Plans as required Maintains paper/electronic TMF and electronic...

Who we are looking for This is what you will do Strategic leadership role within Global Clinical Development, responsible for overseeing Data Management, Biostatistics, and Statistical Programming functions. The position drives the vision, execution, and innovation of clinical data strategies across all phases of drug development, ensuring scientific rigor, operational efficiency, and regulatory...

A leading pharmaceutical company in Parma, Italy, seeks a Clinical Trial Documentation & Records Management Lead to ensure compliance with regulatory standards and manage clinical trial technologies. The ideal candidate has 8-10 years of experience in clinical operations and a robust understanding of eTMF and CTMS. This role emphasizes team leadership, cross-functional collaboration, and...

A leading pharmaceutical company in Parma, Italy, seeks a Clinical Trial Documentation & Records Management Lead to ensure compliance with regulatory standards and manage clinical trial technologies. The ideal candidate has 8-10 years of experience in clinical operations and a robust understanding of eTMF and CTMS. This role emphasizes team leadership, cross-functional collaboration, and...

A global pharmaceutical company in Parma, Italy, seeks a Clinical Pharmacologist Lead with over 5 years of industry experience to oversee clinical pharmacology strategies. Responsibilities include leading Clinical Development Programs, designing trial protocols, and integrating innovative methodologies. The ideal candidate will have an MD or PhD, proven leadership in pharmacokinetics and...

Select how often (in days) to receive an alert:Senior Director, Clinical Biometrics & AnalyticsDepartment: Global Clinical DevelopmentBusiness Area: R&D, Pharmacovigilance & Regulatory AffairsJob Type: Direct EmployeeContract Type: PermanentLocation: Parma, ITAbout usBased in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with 90 years’ experience,...

Business Area: R&D, Pharmacovigilance & Regulatory AffairsJob Type: Direct EmployeeContract Type: PermanentLocation: Parma, ITAbout usBased in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with 90 years’ experience, operating in 31 countries with more than 7,000 employees (Chiesi Group). To achieve its mission of improving people’s quality of life...

Select how often (in days) to receive an alert:Senior Clinical Research Physician Non-Obstructive Respiratory DiseasesDepartment: Global Clinical DevelopmentBusiness Area: R&D, Pharmacovigilance & Regulatory AffairsJob Type: Direct EmployeeContract Type: PermanentLocation: Parma, ITAbout usBased in Parma, Italy, Chiesi is an international research‑focused pharmaceutical and healthcare group with...

Location: Europe - Remote, ITAbout usBased in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with 90 years’ experience, operating in 31 countries with more than 7,000 employees. To achieve its mission of improving people’s quality of life by acting responsibly towards society and the environment, the Group researches, develops and markets innovative...