A global biopharmaceutical organization is looking for a Sr. Clinical Trial Manager to ensure the execution of clinical trials in Italy. This role requires providing medical and scientific leadership, auditing regulatory compliance, and collaborating with cross-functional teams. Candidates should have a Medical Doctor degree or a related Pharma degree and at least 3 years of experience in...
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must...
A leading pharmaceutical company is seeking a Clinical Trial Associate (CTA) in Turbigo, Italy, to provide operational support to the global clinical team. The role is vital in maintaining quality systems and documentation compliance. Ideal candidates will have a Bachelor's degree in a related field and be fluent in both English and Italian. Experience in clinical research and familiarity with...
A 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 Italy. A competitive salary and benefits...
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare...
Regulatory Affairs Manager | Clinical Development (CTA/IND) | EU/US/RoW ABOUT / INFO Regulatory Affairs professional with 7 - 10 years of experience in the pharmaceutical industry, supporting global clinical development programs across EU, US and RoW. Strong track record in managing clinical trial applications and maintenance activities (CTA/IND), coordinating complex submission packages, and...
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. About this role As part of our CDSOphthalmology Trial Master File team you will working...
Una organizzazione di ricerca sanitaria cerca due Data Manager per gestire progetti finanziati dal PNRR. I candidati gestiranno i dati, redigeranno report e garantiranno l'integrità delle informazioni cliniche. È richiesta una laurea magistrale in Biologia e esperienza in ricerca clinica. Offriamo un contratto di Collaborazione Coordinata e Continuativa con un compenso annuale di 28.000 euro. Il...
Location: located in North Italy; Milan Who we are Optimapharm is a globally operating leading mid‑sized full‑service CRO aiming to deliver new therapies to improve and save patients lives. Optimapharm’s key priorities are the well‑being of our people, consistent quality delivery to our clients and healthy sustainable growth. With 26 strategically located offices Optimapharm operates in 40...
A leading pharmaceutical company is seeking a Lead, Trial Delivery Manager in Italy to oversee clinical trial activities, ensuring high-quality execution and vendor relationships. The ideal candidate will have a BS in Life Sciences, 4+ years in clinical trials, and expertise in oncology. Responsibilities include document management, mentoring new team members, and cross-functional coordination....
A leading life science consulting firm is seeking a Regulatory Affairs Manager to support global clinical development programs. The ideal candidate will have 7-10 years of experience in the pharmaceutical industry, with a strong background in managing clinical trial applications, including CTA/IND submissions and compliance with regulatory requirements across EU, US, and RoW. Key skills include...
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,...
Job Overview Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Italy, particularly in our Milan office. Clinical Trial Managers with expertise in Neuroscience and CNS are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. We...
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...
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 Responsibilities - Maintain 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 leading clinical research organization in Turbigo, Italy, seeks a Clinical Research Physician responsible for providing medical leadership for clinical trials. The role involves developing new projects, managing safety issues, and coordinating with various departments. Candidates must have an M.D. degree and prior clinical trial experience. The position offers hybrid work flexibility and...
A leading clinical research organization is seeking Project Coordinators in Turbigo, Italy to engage in the management of clinical trials. The role involves working with operational teams to ensure tasks are completed accurately and on time. Ideal candidates will have a Master's Degree in Life Sciences, excellent communication skills, and attention to detail. The position offers a flexible work...
Due to continuous business growth and a strong study pipeline, we are looking for Project Coordinators to join our successful and growing Italian team and engage in clinical trial management on a day-to-day level. This position will work with our operational teams to accomplish tasks and projects that are instrumental to the company’s success. Responsibilities - Work closely with the Project...
A leading clinical research organization is seeking a Hepatologist to provide medical and scientific leadership for clinical trials in Turbigo, Italy. The role encompasses providing expertise for trial management, contributing to regulatory documents, and coordinating with various departments. Applicants must hold an M.D. degree or equivalent and have prior clinical research experience. The...