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...
Overview On behalf of our Client a global pharmaceutical company IQVIA is looking for Vendor Management Lead Drug Development. The profile will be responsible for selection contracting oversight and performance management of external vendors and collaborators based in Italy supporting clinical development. External vendors include CROs CMOs central labs and bioanalytical labs. External...
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...
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,...
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...
A leading healthcare company is seeking a Manager for Trial Delivery Management in Turbigo, Italy. This role involves overseeing the execution of clinical trial activities, vendor management, and mentoring team members. Candidates should possess a BS in Life Sciences and have at least 8 years of relevant experience in the pharmaceutical or healthcare sectors. Strong leadership and project...
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...
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...
A global clinical research organization in North Italy is seeking a CRA (CRA II-III depending on experience) to conduct independent clinical trial monitoring. The ideal candidate will have at least 2-3 years of experience, a degree in medical or life sciences, and be a certified CRA. Responsibilities include site visits, managing compliance, and negotiating study budgets. This role offers...
Job Description Including, but not limited to the following : - Shape and develop the clinical development plans, while adhering to the highest scientific and ethical standards - Design, conduct and report Sobi-sponsored studies in close collaboration with the rest of the clinical development team, the clinical study teams, regulatory, safety and other cross-functional teams, as applicable -...
Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions. Apply now for the...
Overview Location: based preferably in Milan or Turin | Territory: Lombardia, Piemonte and Liguria. Deadline for Applications: February 6, 2026 The Clinical Sales Representative (CSR) provides clinical support to assigned accounts at a territory or regional level. Activities are driven by account planning (T1 & T2), customer needs, and the BSC sales process aimed at securing the next...
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...
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...
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...
📌 Location 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+...
Clinical Study Administrator (CSA) within Country Operations Management (COM) Responsible for coordinating study activities from start‑up to execution and close‑out, ensuring quality and consistency in trial deliverables and meeting time, cost, and quality objectives in accordance with Good Clinical Practice (GCP), Alexion Standard Operating Procedures (SOPs), and evolving regulatory...
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 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...
We are seeking Clinical Research Physicians to join our dynamic team. The Clinical Research Physician will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review,...