- Remoto
- Tiempo completo
- Contrato
... essential to product validation and regulatory pathways. You will work closely with senior experts and multidisciplinary teams, gaining hands-on experience with clinical investigations, performance studies (ISO 14155 and ISO 20916), technical documentation, and clinical evidence development. Ideal for candidates with 0.5–2 years ...
Spain, Pamplona
Ver vacante- Remoto
- Tiempo completo
- Contrato
... essential to product validation and regulatory pathways. You will work closely with senior experts and multidisciplinary teams, gaining hands-on experience with clinical investigations, performance studies (ISO 14155 and ISO 20916), technical documentation, and clinical evidence development. Ideal for candidates with 0.5–2 years ...
- Remoto
- Tiempo completo
- Contrato
... essential to product validation and regulatory pathways. You will work closely with senior experts and multidisciplinary teams, gaining hands-on experience with clinical investigations, performance studies (ISO 14155 and ISO 20916), technical documentation, and clinical evidence development. Ideal for candidates with 0.5–2 years ...
- Remoto
- Tiempo completo
- Contrato
... essential to product validation and regulatory pathways. You will work closely with senior experts and multidisciplinary teams, gaining hands-on experience with clinical investigations, performance studies (ISO 14155 and ISO 20916), technical documentation, and clinical evidence development. Ideal for candidates with 0.5–2 years ...
Spain, Alacante
Ver vacanteFully remote
... take a consultative approach to trial management, proving to be a valuable partner in trial operational delivery? Precision for Medicine are looking to hire a Clinical Project Manager / Senior Clinical Project Manager with experience in Oncology who have managed full service clinical trials within a CRO setting to join our ...
Fully remote
... take a consultative approach to trial management, proving to be a valuable partner in trial operational delivery? Precision for Medicine are looking to hire a Clinical Project Manager / Senior Clinical Project Manager with experience in Oncology who have managed full service clinical trials within a CRO setting to join our ...
Fully remote
... Summary The Senior Manager, Clinical Operations - Clinical Process Owner is responsible for leading the governance, harmonization, and continuous improvement of Clinical Operations processes across the organization. The role owns the development, simplification, alignment, and lifecycle management of Clinical Operations SOPs, ...
- Híbrido
- Tiempo completo
- Contrato
Permanent contract
About the role We are looking for an experienced Senior Product Manager to join us in Barcelona (Spain) or London (UK). In this position, you will drive the continued development and expansion of Cortellis Clinical Trials Intelligence within our Competitive Intelligence product team. You will serve as the core clinical ...
- Remoto
- Híbrido
- Tiempo completo
... international networks and promoting excellence in the management of cancer among their members. Currently we're looking for a Clinical Project Manager to join our Clinical Operations Team. Main responsibilities: - Responsible for planning, coordinating, and leading all activities and stakeholders involved in a clinical trial to ...
Spain, Barcelona
Ver vacante€140,000 - €200,000 a year
... strategy. This is a remote, field-based position located in Europe, ideally in France or Germany, with convenient access to major transportation hubs and clinical trial sites. The position may be appointed at varying levels depending on the successful candidate's qualifications and experience and will report to the Senior Director ...
- Remoto
- Híbrido
- Tiempo completo
US$212,994 - US$319,492 a year
... multimodal intelligence into clinical development impact through trial enrichment, patient identification, endpoint optimisation, and deeper reanalysis of clinical trial data. In parallel, you will help reinforce foundation models using AstraZeneca's multimodal trial and real-world datasets, creating continuous learning ...
- Híbrido
- Presencial
- Tiempo completo
Full-time hours
... biomarkers, and clinical development. Within AISI, theClinical AI teamsarebuilding world-class AI capability to accelerate the design, conduct, and analysis of clinical trials across ourBioPharmaceuticalspipelines- spanning both early and late phaseprogrammes. We partner closely with clinical development, regulatory, and biometrics ...
- Híbrido
- Tiempo completo
- Contrato
... Domain experience in clinical trials or life sciences. You bring a deep understanding of the clinical development and clinical operations personas, know the clinical ecosystem (EDC, CDMS, CTMS, eTMF), and can engage credibly with clinical operations leaders, medical directors, biostatisticians, data managers, and regulatory ...
Spain, Barcelona
Ver vacanteWork Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Senior Clinical Team Manager PPD’s (a part of Thermo Fisher Scientific) mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it’s you! We know that meaningful results not only require the ...
€70,000 a year
... secondary packaging, labeling, and clinical supplies management services. - Approach and establish strategic relationships with pharmaceutical, biotechnology, and clinical research organizations (CROs) in the Iberia region. - Understand clinical trial portfolios and clients' technical structures to offer CMO/CDMO solutions tailored ...
- Presencial
- Tiempo completo
€48,000 - €68,000 a year
About the role We are seeking an experienced Senior Regulatory Affairs Specialist to join our Clinical Operations team in Spain. This is a Full-time, on-site position where you will play a crucial role in ensuring compliance with regulatory requirements across our clinical trial operations. You will be responsible for managing ...
- Remoto
- Tiempo completo
- Contrato
Full-time hours
... driving impact for customers and defining the pace of patient progress. Job Responsibilities Project Leadership and Delivery: - Manages a project as Project Manager overseeing interdisciplinary clinical research programs ensuring compliance with Good Clinical Practices (GCPs), relevant Standard Operating Procedures (SOPs) ...
... with a solid understanding of software development lifecycles and computerized system validation (CSV) in line with GxP requirements. - You are familiar with clinical trial systems and clinical trial data standards, and can navigate a global matrix organization to build trusted relationships across R&D, IT, and external partners. ...
Spain, Mollet del Vallés
Ver vacanteUS$130,000 - US$170,000 a year
... platform. Trusted by global top MNCs, our innovations accelerate drug development and market entry. We are committed to globalizing AuroraPrime to enhance clinical trials and real-world research by leveraging cutting-edge AI, cloud computing, and big data. We help our clients achieve clinical operational efficiency, automate ...