Empleos de clinical study coordinator en Sevilla

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...

TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a Freelance Clinical Database...

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 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 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,...

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. With deep domain expertise in regulatory sciences, clinical research solutions,...

Clinical Study Lead, Precision Medicine 2 positions | New role within MDx CRO's Precision Medicine team About the role MDx 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,...

Clinical Study Lead, Precision Medicine 2 positions | New role within MDx CRO's Precision Medicine team About the role MDx 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,...

Programmer (SAS & R) with German - Spain-based (remote/hybrid) Madrid, Spain Madrid, Spain Full time R We are looking for a highly motivated **HTA Programmer** (Analyst/Consultant) to support health technology assessment (AMNOG) and market access activities in Germany. The role is ideally suited for **biostatisticians** or **data scientists** with a strong...

Apply for MSR Oncology Hematology (Andalucía) at Pfizer in Sevilla, AN, ES. This Visa sponsorship job abroad position offers great opportunities for career growth. Job Description Medical Affairs Scientist /Medical Scientific Relations (MAS/MSR) function is responsible to create scientific partnership with local KOLs through a qualified approach that...

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 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 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...

Neuroscience Medical Science Liaison - Spain and Portugal Updated: Yesterday Location: Sevilla, Andalusia, Spain Job ID:18424-OTHLOC-CrNwYfws We are seeking a field-based Medical Science Liaison (MSL) to support the Neuroscience and Psychiatry therapy area across international markets. This role is focused on building trusted scientific partnerships...

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...