Empleos de clinical study coordinator en Las Palmas

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 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 role you will lead the configuration and deployment of eTMF, CTMS and related solutions for life sciences customers, ensuring alignment with regulatory and validation needs. You will guide design decisions, deliver training, and support customers through application validation and lifecycle activities. As a Senior Consultant you will...

Overview As a Clinical Scientist Director in Early Development Oncology, you translate scientific strategy into actionable clinical execution in early-phase trials. You provide hands-on oversight of protocol execution, data quality, and medical data review to enable decision-ready data. You collaborate across cross-functional teams to align trials with...

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 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 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...

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...

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...

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...

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 lead the configuration and deployment of eTMF, CTMS and related solutions for life sciences customers, ensuring alignment with regulatory and validation needs. You will guide design decisions, deliver training, and support customers through application validation and lifecycle activities. As a Senior Consultant you will...

Overview In this role you will lead the configuration and deployment of eTMF, CTMS and related solutions for life sciences customers, ensuring alignment with regulatory and validation needs. You will guide design decisions, deliver training, and support customers through application validation and lifecycle activities. As a Senior Consultant you will...

Overview In this role you will lead the configuration and deployment of eTMF, CTMS and related solutions for life sciences customers, ensuring alignment with regulatory and validation needs. You will guide design decisions, deliver training, and support customers through application validation and lifecycle activities. As a Senior Consultant you will...

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...

Overview As a field-based medical expert, you will shape medical strategy and drive data generation in your disease area. You'll build long-term partnerships with TAEs and investigators to deliver value to healthcare professionals, while leading field medical plan execution in collaboration with the Country Medical Manager. You'll translate insights into...