Senior Clinical Research Associate

Trial Form Support is seeking a remote oncology clinical monitors to oversee trials across sites, ensuring patient safety, data integrity and regulatory compliance in a fast-paced setting.The role supports study conduct, site management and quality with GCP/ICH adherence, coordinating monitoring activities and audits while enabling meaningful patient...

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 global clinical research organizationdedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is...

Overview In this role, you will lead site management and monitoring for assigned trials to ensure patient safety and high-quality execution. You will work with cross-functional teams to keep study activities on track from activation to database lock. You will monitor AEs/SAEs and support Drug Safety, audits, and CAPA implementation. This is a remote,...

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 global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is...

Trial Form Support is seeking a remote Clinical Monitor to oversee oncology trials across sites, ensuring patient safety, data integrity, and regulatory compliance. You will coordinate monitoring activities, manage documentation, and participate in audits while supporting study conduct within a global, collaborative team.The role requires a Bachelor's in...

Contract: Initial 12 months, with potential for rolling 12-month extensions We are looking for a Clinical Contracts Associate to manage the preparation, negotiation and execution of clinical trial contracts and budgets across EMEA. You will work directly with research sites and collaborate with legal, compliance and clinical teams to resolve contractual...

** Please submit your application in English **Faccia ora il prossimo passo nella sua carriera: scorra verso il basso per leggere la descrizione completa del ruolo e invii la sua candidatura.What You'll Do:Serve as main CTI contact for assigned study sitesConduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out...

Sr. Site Contracts Associate IQVIA Biotech Italy - HomebasedOverviewWe are seeking an experienced Senior Site Contracts Associate to manage contract strategy and oversee all start‑up contracting activities for selected sponsors. In this role, you will support complex studies and multi‑protocol programs, ensuring high‑quality delivery and operational...

Senior Bioinformatics ScientistIWhat if the work you did every day could impact the lives of people you know? Or all of humanity?At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early...