Senior Regulatory Coordinator, Clinical Trials

A global healthcare technology company is seeking a Clinical Research Coordinator to work part-time in Cona Ferrara. The successful candidate will maintain study documentation, support patient enrollment, and coordinate logistical activities in clinical trials. The ideal applicant will have a Bachelor’s degree in life sciences, at least 1-2 years of...

Employment Opportunities Designed to Help Us Collaborate in Creation! Senior Regulatory Coordinator Position Number: | Department: CBCC Research – HEMATOLOGY - ONCOLOGY (06508A) | Campus: Maywood-Health Sciences Stays current with Federal regulations and can apply that knowledge to work-related activities. Has working knowledge of regulations pertaining to...

Employment Opportunities Designed to Help Us Collaborate in Creation!Senior Regulatory CoordinatorPosition Number: | Department: CBCC Research – HEMATOLOGY - ONCOLOGY (06508A) | Campus: Maywood-Health SciencesStays current with Federal regulations and can apply that knowledge to work-related activities. Has working knowledge of regulations pertaining to...

JOB SUMMARY Senior Clinical Consultant – Life Sciences (Rif. ANN ) We are CPL & Taylor by Synergos, an international digital‑solutions consulting firm specialising in the Life Sciences sector. Based in Italy, we support pharmaceutical and biotech companies across regulatory, pharmacovigilance, clinical trials, medical affairs and quality assurance. The...

Clinical Research Coordinator Cona Ferrara (Part-Time 24 hours / week) Start Date : Immediate Duration : Approximately 1 year IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Cona Ferrara. This part-time position offers a unique opportunity to contribute to meaningful research in a collaborative...

Clinical Trial Manager – Italy | Advanced Clinical (FSP Model) Oncology focused Advanced Clinical is seeking an experienced Clinical Trial Manager to join our UK-based Functional Service Provider (FSP) team. This role will support global clinical studies and requires strong operational, vendor management, and monitoring oversight experience....

**Job summary**: As a **Regulatory Specialist **you will be expected to actively participate in all start up activities and perform CA and EC submissions. You will be responsible for communication with Regulatory Authorities and Ethics Committees and function as an expert for Regulatory issues in Italy. Reporting to **Clinical Operations Manager**, you will...

A leading global clinical research firm is seeking a Clinical Project Manager based in Rome. This role is essential for managing clinical trials and ensuring project delivery within agreed contracts. Responsibilities include collaboration with internal teams, leading study management, and ensuring compliance with clinical guidelines. Required qualifications...

**Job summary**: As a **Clinical Research Associate **you will be expected to actively participate in and manage the recruitment of potential investigators and perform CA and EC submissions. You will be responsible for monitoring of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, liaison with vendors and other duties....

A healthcare organization located in Italy is seeking a Clinical Research Coordinator II to support clinical research projects within the Department of Orthopaedic Surgery. The role includes ensuring regulatory compliance, managing research data, and providing administrative support for grant activities. The ideal candidate should have a Bachelor's degree in...