Empleos de ich en Murcia

OverviewIn 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 support...

Tigermed is seeking a Clinical Research Associate to oversee study site selection, initiation, monitoring, and safety reporting in compliance with protocol and ICH-GCP guidelines. The role includes coordinating materials, training site staff, and ensuring timely documentation throughout the study lifecycle.The ideal candidate will have a Bachelor degree or...

OverviewIn this fully remote role, you will provide GCP compliance guidance to clinical study teams and partners, prioritizing risks to protect study quality. You will act as a trusted advisor across R&D and external vendors, shaping actions to address quality issues and support inspections. You'll lead risk-based compliance activities, drive CAPAs, and...

OverviewIn 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...

OverviewSenior CRAs in Spain join an evergreen talent pipeline to support a strategic sponsor in a collaborative, quality-driven environment. You will monitor studies, ensure compliant conduct, and work across cross-functional teams from site setup to study closeout. The role offers home-based flexibility and opportunities to mentor junior staff and engage...

OverviewAs 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 staff...

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 to proceed with study start and conduct in...

OverviewIn 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 regulatory...

OverviewJoin 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 data...

OverviewIn 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,...

OverviewIn 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 process...

OverviewIn 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...

Overview In this role you lead full-service oncology clinical projects within a CRO setting, driving delivery across global trials and coordinating cross-functional teams. You will oversee client relationships, project scope, budgets, and timelines from proposal through study completion. You work closely with internal and external stakeholders to ensure...

Overview As a Project Director, you lead global oncology clinical trial programs, overseeing study portfolios and cross-functional teams to ensure on-time, within-scope delivery. You partner with clients to align on goals, drive process improvements, and maintain high-quality execution across studies. You shape trial strategy, risk management, and change...

Study Site Specialist – Spain We are seeking an experienced Study Site Specialist to join a global clinical res Search programme. This is a permanent, fully remote position for candidates based in Spain. Location: Spain Working arrangement: Fully remote Employment type: Permanent Position Summary The Study Site Specialist will manage site start-up...

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...

Si le interesa solicitar este empleo, por favor, asegúrese de cumplir los siguientes requisitos que se enumeran a continuación.The Senior Director, Regulatory Affairs is responsible for leading regulatory strategy and execution for assigned development programs, with a primary focus on oncology and broader disease areas as needed. This role will serve as...

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...

Overview In this role you drive late-phase oncology development by turning scientific strategy into executable clinical trials. You lead protocol execution, data quality, and cross-functional collaboration to produce decision-ready data that informs regulatory decisions. You will be a scientific expert across the therapeutic area, guiding investigators,...

The Senior Director, Regulatory Affairs is responsible for leading regulatory strategy and execution for assigned development programs, with a primary focus on oncology and broader disease areas as needed. This role will serve as the Global Regulatory Lead for designated assets and will be accountable for end-to-end regulatory leadership from early...