Full-time hours
... area, clinical development, translational medicine, medical affairs, or related scientific functions is preferred. Nice to have Advanced Analytics, Budget Management, Compliance Management, Critical Thinking, Cross-Functional Collaboration, Data Analysis, Data Privacy Standards, Data Quality, Data Reporting, Data Savvy, ...
Full-time hours
... Product Management strategy. • Connect Microbiology testing to outputs to laboratorio decision making, workflow efficiency, and economic impact to support value based selling. • Develop, customize, and maintain clinical marketing materials: value decks, study digests, application notes, clinical dossiers, and congress communication. ...
Fully remote
... client presentations - Liaise with Project Team and senior management of both Precision and sponsors, including C level - Handle and lead all aspects of a clinical research trial or trials - Total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, ...
Fully remote
... client presentations - Liaise with Project Team and senior management of both Precision and sponsors, including C level - Handle and lead all aspects of a clinical research trial or trials - Total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, ...
Fully remote
... - Lead and represent cross-functional process governance and decision-making, partnering with Clinical Operations, Quality Assurance, Regulatory, Project Management, Data Management, Biostatistics, Medical, Training, and other relevant functions. - Lead process implementation and change management, including impact assessment, ...
- Remoto
- Híbrido
- Tiempo completo
... monitoring reports. - Coordinate regulatory submissions and site activations across multiple countries, ensuring alignment with local requirements and global study timelines. - Support Risk-Based Quality Management (RBQM) and centralized monitoring activities in collaboration with the clinical operations team. Requirements ...
Spain, Barcelona
Ver vacanteFull-time hours
... the identification of the relevant CM elements to be implemented for the study (Quality Tolerance Limits (QTL), Key Risk Indicators, data visualizations and Data Quality Assessments) - Setup/Program QTL, KRI and Data Quality Assessments according to the study CMP - Refresh the Centralized Monitoring Platform at predefined ...
- Remoto
- Tiempo completo
- Contrato
... investigators - Assist with monitoring‐support activities and data‐related tasks - Contribute to scientific and medical writing, including study summaries and evidence-based content - Support literature reviews, background research, and documentation preparation - Assist in drafting components of clinical evidence documentation under ...
Spain, Vitoria
Ver vacante- Remoto
- Tiempo completo
- Contrato
... investigators - Assist with monitoring‐support activities and data‐related tasks - Contribute to scientific and medical writing, including study summaries and evidence-based content - Support literature reviews, background research, and documentation preparation - Assist in drafting components of clinical evidence documentation under ...
... line management and/or project management). Key Responsibilities Technical - Previous experience with SAS and some R experience/knowledge. - Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs - Author, review and approve study TFL shells and dataset specifications - Author, validate and document ...
... performed by others and provide feedback regarding interview technique and scoring. Responsibilities include: - Review of scalesadministered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manner to ensure data reliability. - Evaluation the quality of assessments, conducting ...
Spain, Barcelona
Ver vacante- Remoto
- Tiempo completo
- Contrato
... scientific backgrounds eager to enter the industry. Support the preparation and execution of Clinical Investigations and Performance Studies - Assist with monitoring‑support activities and data‑related tasks - Contribute to scientific and medical writing, including study summaries and evidence-based content - Support literature ...
Spain, Pamplona
Ver vacante- Remoto
- Tiempo completo
- Contrato
... scientific backgrounds eager to enter the industry. Support the preparation and execution of Clinical Investigations and Performance Studies - Assist with monitoring‑support activities and data‑related tasks - Contribute to scientific and medical writing, including study summaries and evidence-based content - Support literature ...
- Remoto
- Tiempo completo
- Contrato
... scientific backgrounds eager to enter the industry. Support the preparation and execution of Clinical Investigations and Performance Studies - Assist with monitoring‑support activities and data‑related tasks - Contribute to scientific and medical writing, including study summaries and evidence-based content - Support literature ...
- Remoto
- Tiempo completo
- Contrato
... scientific backgrounds eager to enter the industry. Support the preparation and execution of Clinical Investigations and Performance Studies - Assist with monitoring‑support activities and data‑related tasks - Contribute to scientific and medical writing, including study summaries and evidence-based content - Support literature ...
Spain, Alacante
Ver vacante... line management and/or project management). Key Responsibilities Technical - Previous experience with SAS and some R experience/knowledge. - Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs - Author, review and approve study TFL shells and dataset specifications - Author, validate and document ...
9k
... requirements (cost, quality, and time). - Review the necessary documentation before (e.g. Protocol, ICF, etc.), during (e.g. Monitoring etc.) and at the end (e.g. Study Report, etc.) of clinical trials. - Coordinate internal Chemo activities and procedures related with the conduct of the clinical trials (e.g. investigational ...
Spain, Guadalajara
Ver vacanteFully remote
... meaningfully - your voice will be heard. Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management. Precision for Medicine is looking for Clinical Research Associates II based in Madrid or Barcelona to join our team in Spain. About you - You are calm, thoughtful, ...
€140,000 - €200,000 a year
... demonstrating competency in CT and echocardiographic imaging, applicable clinical study documentation and Instructions for Use, procedural best practices, clinical evidence, approved product messaging and the competitive landscape. - Interface with clinical trial sites, demonstrating expertise in all technical aspects ...