Work Schedule7 1/2 hr shift Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description
As a CRA II at ICON, you design and analyze clinical trials, ensuring data integrity and patient safety while advancing innovative therapies. You will monitor sites, collaborate with investigators, and contribute to study documentation. This role
Hire Feed is seeking a Biological Scientist to join a remote, full-time role focused on biological research to support product development. You will design and execute experiments, analyze data with scientific software, and report findings to inform
In 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 data
In this role you join Medpaces Clinical Monitoring team in Italy to perform site monitoring, qualification, initiation, and closeout visits while ensuring protocol and regulatory compliance. You will verify investigator qualifications, manage data integrity, and support site
Planet Pharma are currently partnered with an exciting global CRO and we are actively seeking an experienced Clinical Research Nurse to join the business on a freelance basis. This is an ad-hoc role in Brescia. Key Responsibilities:
Evidilya, CRO digital-native del Gruppo SPRIM., che Progetta e conduce studi interventistici e Real-World Evidence su scala globale nei settori Pharma, Consumer Healthcare, Medical Devices e Food & Nutrition ricerca In-House Clinical Research Associate che guidi lunità
Planet Pharma are currently partnered with an exciting global CRO and we are actively seeking an experienced Clinical Research Nurse to join the business on a freelance basis. This is an ad-hoc role in Brescia. Key Responsibilities:
Clinical Contracts Associate – Italy Location: Remote, Italy – open to candidates based anywhere in Italy Employment Type: Full-Time, 12-Month Fixed-Term Contract Hours: 40 hours per week Start Date: To be confirmed Project Status: Pipeline opportunity,
Job SummaryMedpace 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
Job OverviewThe medical department consists of a Chief Medical Officer, Medical Directors, Sr Medical Directors, Medical Writers, and Safety Associates. The Medical Director provides medical and scientific support to clinical research programs, study teams and investigators. The
Job SummaryWe are seeking a Psichiatry 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
Medpace is seeking an Experienced Clinical Research Associate (CRA) to join the Clinical Monitoring team in Italy. You will conduct site visits, verify investigator qualifications, and ensure protocol and regulatory compliance to support trials from initiation through closeout.
Quality Assurance (GCP) Specialist Company Description Phidealive S.r.l. is an independent Italian full-service Contract Research Organization (CRO) operating as a Clinical Research Atelier. Unlike large global CROs, we work through a selective, highly tailored model, combining scientific expertise, regulatory
In this role you will provide medical leadership for clinical trials, guiding scientific strategy, trial execution, and reporting. You will serve as the internal medical expert for study results interpretation and contribute to protocol and project design.
Your mission As a Business Developer, you will play a key role in expanding SPIN360s client portfolio and strengthening our market presence, with a primary focus on the fashion & luxury, leather & tanning, agroindustry, chemicals,
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation What Youll Do Study & Site Support Complete assigned study and site management
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Were looking for a Clinical Research Associate II (CRA II) to join our growing Clinical Operations team in Italy. If youre passionate about clinical research, enjoy building strong site relationships, and