Offerte di lavoro study start up unit – Roma

Every clinical trial begins with a critical first step – getting sites ready to enroll patients. In this role, you'll be the driving force behind regulatory and ethics submissions that open the door for breakthrough therapies to reach the people who need them. Scopra di più sui compiti quotidiani, le responsabilità generali e l'esperienza richiesta per...

Novo Nordisk is seeking a Senior Study Start-up Specialist in Italy to drive regulatory submissions and site activations for clinical trials. You will manage end-to-end study start-up, ensuring timely approvals and compliance with local and international regulations. You will coordinate with internal and externalStakeholders, maintain trial master file, and...

Every clinical trial begins with a critical first step – getting sites ready to enroll patients. In this role, you'll be the driving force behind regulatory and ethics submissions that open the door for breakthrough therapies to reach the people who need them. Your new role As a Senior Study Start-up Specialist, you will play a pivotal role in enabling...

Overview In this role, you drive the study start-up process to enable timely, compliant trial initiation. You manage regulatory and ethics submissions and coordinate cross-functional colleagues to activate sites and enable patient access to investigational therapies. You will operate within a global trial portfolio, supporting continuous improvement and...

Novo Nordisk A/S in Italy is seeking a Senior Study Start-up Specialist to drive regulatory submissions and site activation for clinical trials, ensuring compliance with ICH-GCP and local requirements.Il suo CV è pronto? Se sì, e se è convinto/a che questo sia il ruolo giusto per lei, si candidi il prima possibile.You will manage end-to-end start-up,...

Novo Nordisk Pharma seeks a qualified professional to drive study start-up processes, enabling timely trial initiation. You will handle regulatory submissions, coordinate cross-functional teams, and ensure ICH-GCP compliance across projects withinItaly.The role emphasizes collaboration with local Italian teams, quality documentation, and stakeholder...

CTI Clinical Trial and Consulting Services in Italy seeks a Clinical Research Associate to serve as main CTI contact for assigned study sites and to conduct monitoring visits in line with ICH-GCP. You will support start-up activities, manage essential regulatory documents, participate in team meetings, and help ensure accurate IP storage and trial...

Novo Nordisk A/S in Italy is seeking a Senior Study Start-up Specialist to drive regulatory submissions and site activation for clinical trials, ensuring compliance with ICH-GCP and local requirements. You will manage end-to-end start-up, coordinate with internal and external stakeholders, maintain trial master file, and support contracts and budgets in a...

Every clinical trial begins with a critical first step – getting sites ready to enroll patients. In this role, you'll be the driving force behind regulatory and ethics submissions that open the door for breakthrough therapies to reach the people who need them. Your new role As a Senior Study Start-up Specialist, you will play a pivotal role in enabling...

BeiGene, Ltd. is seeking a Regional Clinical Trial Management Associate in Italy (remote). The role supports the Regional Clinical Study Manager in regional study delivery, oversees feasibility, start-up, document generation, and TMF tasks, and coordinates regional meetings and communications. A background in clinical research within biotech/pharma/CRO is...

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. General Description Supports the Regional Clinical...

Overview In this role you support regional clinical study delivery to ensure trials run on time, within budget, and to quality standards. You collaborate with the Regional Clinical Study Manager, global teams, and site staff to coordinate feasibility, start-up, TMF, and site communications. You gain hands-on experience in clinical operations and regulatory...

Work ScheduleLe interessa questa opportunità? Si candidi in fretta, è previsto un elevato volume di candidature. Scorra verso il basso per leggere la descrizione completa.Standard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionSenior Clinical Team ManagerPPD's (a part of Thermo Fisher Scientific) mission is to improve health. It starts as an idea to...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Senior Clinical Team Manager PPD's (a part of Thermo Fisher Scientific) mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it's you! We know that meaningful results not only require the right approach, but also the...

** Please submit your application in English ** What You'll Do: Serve as main CTI contact for assigned study sites Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable...

Clinical Trial Administrator Salary : €36,640 - 53,130 yearly Azienda : Novo Nordisk Tipo Lavoro : Full Time Italy Descrizione Lavoro - Clinical Trial Administrator Clinical Trial Administrator (Fixed Term, One Year Contract) Research & Development, Clinical Development Centre Italy Rome, Italy Every clinical trial that reaches patients depends on...

SENIOR PYTHON DEVELOPER | SCIENTIFIC DATA | LONG-TERM FREELANCE We're partnering with a leading Italian technology and digital engineering consultancy that delivers software engineering, data, AI and digital transformation solutions for major organisations across Europe. They are currently looking for one experienced Senior Python Developer to join a...

BeiGene, Ltd. is seeking a Regional Clinical Trial Management Associate in Italy (remote). The role supports the Regional Clinical Study Manager in regional study delivery, oversees feasibility, start-up, document generation, and TMF tasks, and coordinates regional meetings and communications.A background in clinical research within biotech/pharma/CRO is...

Nestlé Purina PetCare - HR Business Partner - Mantova Salary: €65,000 - 65,000 yearly Azienda: Nestlã© Tipo Lavoro: Full Time Italy Descrizione Lavoro - Nestlé Purina PetCare - HR Business Partner - Mantova At Nestlé Purina we are committed to creating richer lives for pets and the people who love them, providing high-quality nutrition for cats...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join us as a Country Approval Specialist and make an impact at the forefront of innovation. We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our...