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 our Milan office. Clinical Trial Managers with expertise in
A leading clinical research organization is looking for a Clinical Trial Manager in Turbigo, Italy. The ideal candidate will manage clinical trial operations, maintain in-depth knowledge of protocols, and provide oversight to project teams. Candidates with
A leading clinical research organization in Italy is seeking a Clinical Trial Manager to oversee project operations within a fast-paced environment. Ideal candidates will have at least 2 years of experience in clinical trial management and
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
Experteer OverviewJoin Medpace as a Clinical Research Associate in Italy, working full-time from home or office with a Clinical Monitoring team. You will help ensure trials run in line with protocols, GCP, and regulatory standards, while collaborating
Our Site Contracts Team is currently seeking a Clinical Trial Contract Specialist to join our Site Contracts Team in Italy. This position plays a key role in the study start‑up and clinical trial management processes at
Medpace is seeking a Clinical Trial Contract Specialist for its Site Contracts Team in Turbigo, Italy. This role involves drafting, negotiating, and finalizing contracts for clinical studies, ensuring alignment with local regulations and internal processes. Candidates should
Experteer Italy is looking for a Clinical Research Associate to join Medpaces Clinical Monitoring team in Lombardia. The role involves site monitoring, ensuring regulatory compliance while traveling up to 60-80% nationwide.You will conduct qualification and closeout visits,
Experteer OverviewIn this role you support Medpace’s clinical monitoring efforts across Italy, enabling high-quality, compliant trials. You will join a cross-functional team to conduct site visits, verify data and investigator qualifications, and ensure regulatory adherence. The position
Experteer OverviewIn this role you join Medpaces Clinical Monitoring team in Italy to perform site-based monitoring activities for clinical studies. You will receive comprehensive training and work either remotely or from an office, contributing to study integrity
Experteer OverviewIn this full-time role, you join Medpace’s Clinical Monitoring team to support site-based trials in Italy, helping advance clinical development for diverse therapies. You will perform monitoring visits, ensure protocol and regulatory compliance, and contribute to
We are seeking a Dermatologist – Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical
We are seeking a Hepatologist to join our team in London. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally,
A leading clinical research organization in Italy is seeking a Dermatologist – Medical Director to lead and manage clinical trials while providing medical expertise. This role involves developing new clinical projects, managing safety issues, and closely
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
Experteer OverviewIn this role you will provide medical, scientific and strategic leadership for planning, executing, and reporting clinical trials. You will serve as Medpace’s internal medical expert and support review and interpretation of results in study reports.
The Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For
Overview As a Site Contracts Specialist you’ll own the contract lifecycle for clinical studies, from drafting to finalization, within Medpace’s Site Contracts Team in Italy. You will negotiate within approved templates, assess risks, and coordinate with internal
Experteer Overview In this CRA role at Medpace you will support the integrity of clinical studies across pharmaceutical and medical device development. You’ll join a training-focused program (PACE) that accelerates your skills toward independent CRA responsibilities. You
Medpace, Inc. is looking for Clinical Trial Managers to join our team in Milan. This position allows professionals with expertise in Immunology and Infectious Diseases to manage clinical projects while providing remote flexibility based on experience. Successful