Fully remote
... 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 global team. In this pivotal role you will have full service oversight for clinical projects across global/regional ...
Fully remote
... 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 global team. In this pivotal role you will have full service oversight for clinical projects across global/regional ...
- Híbrido
- Presencial
- Tiempo completo
- Contrato
€27,900 - €51,900 a year
... contribute to analytics, reporting, or visualization solutions that support business decisions and operational insights. - Awareness of clinical research and clinical trial operations, including familiarity with Clinical Data Operations, Good Clinical Practice, Electronic Data Capture systems, or Clinical Data Interchange ...
Spain, Barcelona
Ver vacante- 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 ...
What you'll do - Responsible for executing one or more elements of clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, and AbbVie policies and procedures). - Supports the Study Project Manager in leading the cross functional study team: o -Supports the preparation of Clinical Study Team meetings ...
- 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
- 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 vacantede 50000 a 85000 €/año
... application package and follow up via email with our decision. - If moving to the interview stage, the process is as follows: - A conversation with the hiring manager - A practical case exercise - A final conversation with our group's Senior Leader. - Once all interviews are complete, the manager will be in touch with a final ...
Full-time hours
About the role The Clinical Marketing - Microbiology develops and executes clinical marketing strategies that strengthen the clinical value, scientific evidence, and differentiated positioning of the Microbiology in Iberia. Working closely with the Product Managers, the role converts clinical data, realworld insights, and ...
€70,000 a year
... forecasts and activity reports to management. - Collaborate with operations, quality assurance, and project management teams to ensure a smooth onboarding of new clinical supplies projects. - Analyze competitor offerings and their pricing strategies within the secondary packaging and clinical logistics sector. What you'll get ...
- 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 vacanteFull-time hours
... communicating with all levels of personnel and participating in collaborative work team (locally and globally). - Advanced knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices. - Excellent command, both verbal and written, of English This role is not eligible for UK visa sponsorship ...
- Remoto
- Híbrido
- Presencial
- Tiempo completo
- Contrato
€63,000 - €65,000 a year
... HealthScience, you will be part of a global team dedicated to advancing innovative therapies and improving patient outcomes. We are looking for an experienced Clinical Research Manager (CRM) to join our Ophthalmology team and play a key role in overseeing clinical trial operations across multiple studies and countries. This ...
... we're looking for - Minimum of a Master's degree (MA/MS) in Psychology, Counseling, Psychiatric, Nursing or Social Work, or equivalent. - Minimum of 3 years of clinical experience working with schizophrenia and major depressive disorder populations . - Minimum of 3 years of clinical experience working a dministering psychiatric ...
Spain, Barcelona
Ver vacante9k
... sustainable development. Ready to become a #Challenger? What are we looking for? Planning, designing, organization, supervision of conduct and reporting of clinical trial contracted to Clinical Research Organizations (CRO) to enable studies execution within the planned timelines and in compliance with current GCP and other ...
Spain, Guadalajara
Ver vacanteFully remote
... handling conflict by using tried and true resolution strategies. How we will keep you busy and support your growth You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations ...