- Clinical Research Associate
- Clinical Project Manager
- Senior Clinical Research Associate
- Medical Science Liaison
- Associate Director
- Associate Medical Science Liaison
- Tricare Beneficiary Service Representative
- Clinical Trial Manager
- Medical Scientist
- Director
- Accounts Director
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Senior Clinical Research Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the
Clinical Research Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart
Clinical Research Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart
Experienced Clinical Research Associate, Italy Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices in accordance with regulatory requirements,
If you are an experienced Senior CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you! Translational Research in Oncology (TRIO) is a
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every clinical development
Veeda Lifesciences is seeking a Clinical Research Associate (CRA) based in Italy for its growing international hematology/oncology Clinical Trials program. The position is offered on a freelance basis. Job overview: The CRA is responsible for ensuring that the conduct
Your new company Our client is a leading company in the Pharma Sector. We are seeking a Senior Clinical Research Associate to join our team You new role Ensure compliance with client SOPs, study protocols, ICH-GCP and applicable
Career CategoryMedical Affairs Job Description HOW MIGHT YOU DEFY IMAGINATION? Do more with the knowledge you’re working hard to acquire and the passion you already have. At Amgen our shared mission—to serve patients—drives all that we
Get to know us Ideals is a global B2B SaaS product company recognized as the most highly rated and customer-centric brand in the secure business collaboration market. Trusted by over 2,000,000 users from 300,000 companies globally,
Job Overview Provide foundational and intermediate-level data management expertise to the Clinical Data Management (CDM) team. Support the delivery of high-quality, compliant, and efficient data management outputs that meet internal and external customer requirements. May also contribute
We are the people who give possibilities purpose BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it’s no small feat. It takes
Are you being referred to one of our roles by a connection in Alira Health? If so, please apply using the referral link emailed to you. Join our global team dedicated to innovation and initiative, where
Cosmo is an innovative company focused on medical technologies (MedTech), active in the development of solutions based on artificial intelligence, dermatology, gastrointestinal diseases, and CDMO services. We collaborate with global partners to create solutions that improve
Regional CRA – Oncology | Italy | Remote | FSP We are supporting an advanced global FSP partnership with a US-based oncology biotech seeking an experienced Regional CRA to join a high-performing clinical operations team. This is
OverviewAs a Clinical Research Associate at Alira Health, you will lead site monitoring for clinical trials with independence and collaboration. You’ll work with in-house CRAs, Lead CRAs, and project managers to ensure protocol compliance, address site questions, and support
Experteer OverviewIn this role you will independently conduct site monitoring for clinical trials to ensure protocol compliance and data integrity. You will collaborate with in-house CRAs, Lead CRAs, Directors, and Project Managers to address site questions, support
Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions Perform
UBC is looking for a Lead Clinical Research Associate to provide oversight and support to clinical projects. You will ensure compliance with guidelines while mentoring the project team. The ideal candidate must have over 5 years of site management
Parexel is pleased to announce we are looking to hire several CRA II for the team in Italy. Candidates must have close to atleast 2 years independent monitoring experience in a similar setting. The role can