Empleos de ich en Zaragoza

Overview In this evergreen role, you help drive clinical studies for a strategic sponsor in a highly collaborative, quality-focused environment. Based in Spain with remote options, you will monitor sites, ensure trials align with protocol and standards, and support study setup and regulatory activities. You may train junior staff and engage directly with...

Overview In this evergreen role, you help drive clinical studies for a strategic sponsor in a highly collaborative, quality-focused environment. Based in Spain with remote options, you will monitor sites, ensure trials align with protocol and standards, and support study setup and regulatory activities. You may train junior staff and engage directly with...

Overview In this evergreen role, you help drive clinical studies for a strategic sponsor in a highly collaborative, quality-focused environment. Based in Spain with remote options, you will monitor sites, ensure trials align with protocol and standards, and support study setup and regulatory activities. You may train junior staff and engage directly with...

Overview In this evergreen role, you help drive clinical studies for a strategic sponsor in a highly collaborative, quality-focused environment. Based in Spain with remote options, you will monitor sites, ensure trials align with protocol and standards, and support study setup and regulatory activities. You may train junior staff and engage directly with...

Overview In this CRA II role, you will oversee clinical trial activities to ensure protocol and regulatory compliance across sites. You will work closely with site teams and cross-functional partners to monitor data integrity, patient safety, and trial progress. You’ll apply risk-based monitoring techniques and drive site performance improvements to...

Overview As Director, Study Start Up-EU you lead the SSU group across the region, aligning strategy with project delivery and client expectations. You'll partner with PM, Clinical Leadership and Business Development to ensure smooth regulatory submissions, site activation and contract alignment. You drive operational excellence, manage risk, and develop...

Overview In this senior role, you drive the creation of high-quality clinical study documents, from planning through QC, aligned with regulatory standards. Your expertise shapes content strategy, standards, and processes for global regulatory submissions. This is a hands-on writing leadership role with a clear focus on precision, deadlines, and impact on...

Overview In this senior role, you drive the creation of high-quality clinical study documents, from planning through QC, aligned with regulatory standards. Your expertise shapes content strategy, standards, and processes for global regulatory submissions. This is a hands-on writing leadership role with a clear focus on precision, deadlines, and impact on...

Overview In this senior role, you drive the creation of high-quality clinical study documents, from planning through QC, aligned with regulatory standards. Your expertise shapes content strategy, standards, and processes for global regulatory submissions. This is a hands-on writing leadership role with a clear focus on precision, deadlines, and impact on...

Overview In this senior role, you drive the creation of high-quality clinical study documents, from planning through QC, aligned with regulatory standards. You will collaborate with sponsors, vendors, and internal teams to ensure timely, compliant manuscripts and templates. Your expertise shapes content strategy, standards, and processes for global...

Overview In this role you ensure regulatory compliance and oversee safety reporting for medical products. You will manage SAE processing, ensure data quality, and support audits while collaborating with cross-functional teams to deliver safety insights. The position sits at the intersection of pharmacovigilance, medical oversight, and client delivery,...

Overview In this remote role, you provide Quality Assurance support for Global Medical Affairs Vendor & Third-Party Management, handling quality events, investigations, CAPAs, audits, and due diligence. You collaborate with cross-functional partners to ensure compliance, risk management, and audit readiness across third-party activities. You will lead...

Overview In this remote role, you provide Quality Assurance support for Global Medical Affairs Vendor & Third-Party Management, handling quality events, investigations, CAPAs, audits, and due diligence. You collaborate with cross-functional partners to ensure compliance, risk management, and audit readiness across third-party activities. You will lead...

Overview In this role you drive and oversee multi-site oncology trials within a global program, acting as the primary client liaison and ensuring study delivery meets scope, quality, and budget goals. You'll lead cross-functional teams, shape trial strategy, and support business objectives through process improvement and proactive risk management. The...

Iisaragon is seeking a Mid-Level Research Support Officer (Group C) to assist with nutrition and hepatology studies.Todos los candidatos deben asegurarse de leer atentamente la siguiente descripción del puesto y la información antes de enviar su solicitud.You will work under the PI to perform nutritional assessments, collect dietary data, and support...

Overview Join Precision for Medicine as a Clinical Project Manager/Senior CPM to lead end‑to‑end global oncology trials in a CRO environment. You will drive project delivery, manage cross‑functional teams, and maintain client relationships, budgets, and timelines from proposal through study completion. You’ll ensure quality and coordination across...

University Mid-Level Research Support Officer – Group CPara presentar una candidatura, simplemente lea la siguiente descripción del puesto y asegúrese de adjuntar los documentos pertinentes.Reference number: HR-26/031Start Period: Monday, July 6, 2026End Period: 23:59 p.m. on Thursday, July 16, 2026Required requirements:Hold a Bachelor's Degree in Human...

Responsibilities(a) Site management•     Study site selection, initiation (SIV) and clinical monitoring.•     Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.•     Prepare and conduct SIV to ensure adequate study...

Responsibilities (a) Site management Study site selection, initiation (SIV) and clinical monitoring. Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff...

Study Site Specialist – SpainWe are seeking an experienced Study Site Specialist to join a global clinical resSearch programme. This is a permanent, fully remote position for candidates based in Spain.Location: SpainWorking arrangement: Fully remoteEmployment type: PermanentPosition SummaryThe Study Site Specialist will manage site start-up activities in...