Empleos de cro en Murcia

Overview As Account Partner for Veeva Development Cloud, you will cultivate strategic CRO relationships and drive opportunity generation in Europe. You'll manage complex SaaS sales cycles, coordinate with cross-functional teams, and align client needs with Veeva's development cloud solutions. Your work supports the growth of a mission-driven organization...

Clinical Study Lead, Precision Medicine2 positions | New role within MDx CRO's Precision Medicine teamAbout the roleMDx CRO is creating two new Clinical Study Lead positions within our Precision Medicine Clinical Alliances team.This is not a conventional CRA role. It is not a purely regulatory role either.It sits where biomarker science, investigational...

SAGEA Group is seeking Field Trialists to plan, implement, and manage field trials across Spain in Seville, Murcia and Logroño. You will follow Good Experimental Practices and GLP/BPL standards, adhering to protocols and internal SOPs, and deliver comprehensive reports in technical English.Ideal candidates bring 2–3 years CRO/academic/industry experience,...

SAGEA Group is hiring three Field Trialists in Spain (Seville, Murcia and Logroño areas).The Field Trialist has to plan, implement and manage field trials following Good Experimental Practices (GEP/EOR) and Good Laboratory Practices (GLP/BPL) according to protocols/study plans and internal standard operation procedures.The experimentalist will have the...

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 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 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 will define and drive the technical roadmap for innovative statistical programming. You will evaluate AI-assisted tools to boost efficiency, quality, and regulatory compliance, and replace manual SAS workflows with automated pipelines using R, Python, or emerging tech. You will design reusable tools and guide migration to...

Overview In this Global Clinical Project Manager II role, you will support late-phase Hematology and Immunology trials for sponsor programs. You will liaise with CROs and vendors, keep the project team aligned on timelines, and contribute to study documents and risk templates. You'll drive end-to-end trial execution from start-up through close-out,...

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...

Overview As Statistical Scientist Director, you will lead statistical strategy for key client studies, acting as primary liaison among sponsors and internal teams. You will shape design, analyses, and interpretation, and oversee statistical deliverables from protocol planning to reporting. You'll translate complex quantitative concepts for non-statistical...

Experienced Principal Biostatistician sought for a global CRO to provide statistical leadership on clinical trials, lead studies and submissions, mentor juniors, and collaborate with clients and teams. Fully home-based role.

This position is open across Europe! Kapadi is a full service CRO that focuses on complex oncology indications including immunotherapy and cellular therapies. We know that innovative research requires innovative operations and we've built that into our culture, systems and processes. We have an infrastructure to enhance access to patients and integrated...

This position is open across Europe!Kapadi is a full service CRO that focuses on complex oncology indications including immunotherapy and cellular therapies. We know that innovative research requires innovative operations and we've built that into our culture, systems and processes. We have an infrastructure to enhance access to patients and integrated...