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...
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...
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 -...
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...
At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a more connected compassionate world. A Day in the Life The Clinical Evaluation Medical Writer at Medtronic plays a pivotal role in the Clinical Job Family, specializing in the critical review and...
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...
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...
A leading Contract Research Organization is seeking a Lead Data Manager in Turbigo, Italy. The role involves acting as the primary communication point for project teams and clients, overseeing all data management activities, and ensuring adherence to project timelines and budgets. Ideal candidates will have at least five years in the CRO industry, experience with CDM/EDC systems, and strong...
📌 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+...
Overview Overview We are seeking an experienced and highly organized Associate Director, Global Rare Medical Project Lead to support efficient, compliant, and scalable Medical Affairs execution across Alnylam’s Global Rare franchise. This role strengthens medical ways of working, drives operational excellence, and enables high-quality execution of medical strategies across multiple markets. You...
We’re working with a global healthcare technology provider delivering large-scale hospital information systems and digital health platforms across public and private sector organisations. They are seeking an experienced Project Manager to lead the successful delivery of Electronic Medical Record (EMR) / Health Information System (HIS) implementations. This is a client-facing leadership role,...
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...
Job Overview Responsible for management and service delivery excellence for assigned projects, covering single or multiple Lifecycle Safety functions (clinical trial and/or post-market). Provide leadership and accountability for customer-facing activities and oversight of operational service delivery, working cross-functionally and across the opportunity lifecycle, integrating delivery into one...
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...
Overview PSI is a leading Contract Research Organization with 30 years experience in the industry, offering a balance between stability and innovation to clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while...
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 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...
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,...