Lavoro clinical trial Emilia-Romagna

Select how often (in days) to receive an alert: Clinical Trial Documentation & Records Management Lead Department: Global Clinical Development Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT About us Based in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with...

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...

Sr. Clinical Trial Manager (Clinical Research Medical Advisor) – FSP – Homebased – Italy Join to apply for the Sr. Clinical Trial Manager (Clinical Research Medical Advisor) – FSP – Homebased – Italy role at Syneos Health. Company Overview Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical,...

Planet Pharma is seeking a Clinical Trial Associate (CTA) to provide key operational and administrative support to a global Clinical team. This role plays an important part in maintaining quality systems, training compliance, documentation and clinical platforms, helping to ensure efficient and compliant clinical development activities.Key ResponsibilitiesMaintain and regularly update SOP...

A clinical research organization is seeking a Psychiatry Medical Director to lead medical, scientific, and strategic efforts in clinical trials. The role involves providing expertise in study design and safety management while ensuring compliance with research protocols. Ideal candidates should hold an M.D. degree, with preferred experience in clinical trial research and pharmaceutical...

A renowned Contract Research Organization in Milan is seeking a Clinical Trial Assistant to support project execution from start to finish. The ideal candidate will have a Master's Degree in a scientific discipline or health care, possess strong organizational and decision-making skills, and be fluent in English. This role involves managing study documents, evaluating study sites, and...

A leading life sciences company in Italy seeks a Clinical Study Administrator to coordinate study activities and manage trial documentation in compliance with regulatory standards. The ideal candidate will have a Bachelor's degree in a related field, along with at least 2 years of relevant experience. Strong collaboration, organizational skills, and proficiency in MS Office are essential. The...

A leading healthcare intelligence organization is seeking a Clinical Site Associate to support clinical trial operations. The role requires managing site communications, coordinating trainings, and maintaining essential documentation. Ideal candidates will have a Bachelor's in life sciences, experience in clinical research, and strong organizational skills. This position is office-based with...

A leading biopharmaceutical solutions organization is looking for a Sr. Clinical Trial Manager (Clinical Research Medical Advisor) to provide medical and scientific leadership for clinical trials in Italy. In this homebased role, you will lead trial implementation, support regulatory interactions, and ensure compliance with standards. The ideal candidate has a Medical Doctor degree or equivalent...

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...

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...

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...

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...

Select how often (in days) to receive an alert: Clinical Trial Documentation & Records Management Lead Department: Global Clinical Development Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT About us Based in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with...

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...

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...

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...

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...

On behalf of our Client a global pharmaceutical company, IQVIA is looking for a e-TMF Specialist - Supply section who can join an exciting working environment in a dynamic atmosphere.RESPONSIBILITIES:- To review eTMF plans- To upload documents in the eTMF and perform ongoing quality control of the eTMF (Investigational products and Clinical Trial Supply section) using Company System- Monitor the...