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 ...
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, ...
Fully remote
... looking for - Graduate, postgraduate, 4-year college degree - Experience in a CRO/healthcare field - Relevant experience in drafting, reviewing and negotiating site Clinical Trial Agreements, Vendor Contracts and Site Budget negotiations, but no less than 5 years’ experience. - Experienced leading interactions with Study ...
Fully remote
... looking for - Graduate, postgraduate, 4-year college degree - Experience in a CRO/healthcare field - Relevant experience in drafting, reviewing and negotiating site Clinical Trial Agreements, Vendor Contracts and Site Budget negotiations, but no less than 5 years’ experience. - Experienced leading interactions with Study ...
- 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 ...
... on their skills, qualifications, and relevant experience as outlined in their CVs. Interviews: Meetings may be held with Talent Acquisition and/or the hiring manager. Practical assessment: Depending on the role, candidates may complete a case study, technical task, presentation, or written exercise, on-site or remotely. ...
Spain, Barcelona
Ver vacante... 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 vacante... experience in clinical research, study start-up, regulatory affairs, or a related scientific environment, including international experience. - Strong knowledge of clinical trial regulations, GCP, ICH guidelines, and the drug development process. - Proven experience managing complex, multi-country clinical trial start-up activities. ...
Full-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 ...
Fully 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 ...
€140,000 - €200,000 a year
... optimal clinical outcomes. - Maintain in-depth knowledge of existing DurAVR clinical data and the evolving structural heart evidence landscape. - Support the Clinical and Regulatory Operations teams with site communications, data compliance activities, screening review efficiency and site submission requirements. - Attend ...
- Remoto
- Tiempo completo
- Contrato
... clinical research or R&D — or strong scientific backgrounds eager to enter the industry. Responsibilities You will: - Support the preparation and execution of Clinical Investigations and Performance Studies - Assist in developing study documentation (protocols, CRFs, ICFs) - Collaborate with study sites and internal teams ...
Spain, Vitoria
Ver vacante- Remoto
- Tiempo completo
- Contrato
... clinical research or R&D — or strong scientific backgrounds eager to enter the industry. Responsibilities You will: - Support the preparation and execution of Clinical Investigations and Performance Studies - Assist in developing study documentation (protocols, CRFs, ICFs) - Collaborate with study sites and internal teams ...
Full-time hours
About the job JOB DESCRIPTION: Main Purpose of the Role • This is a sales position where the individual is responsible for servicing the current customer base, increasing sales within that base and establishing new accounts.
- Remoto
- Tiempo completo
- Contrato
Clinical Research and Regulatory Specialist | MedTech Location: Spain (Remote) Full-time We are looking for a motivated junior professional who wants to develop their career in the MedTech and IVD sector. As a Clinical Research and Regulatory Specialist , you will support clinical research activities, scientific and medical ...
Spain, Pamplona
Ver vacante- Remoto
- Tiempo completo
- Contrato
Clinical Research and Regulatory Specialist | MedTech Location: Spain (Remote) Full-time We are looking for a motivated junior professional who wants to develop their career in the MedTech and IVD sector. As a Clinical Research and Regulatory Specialist , you will support clinical research activities, scientific and medical ...
- Remoto
- Tiempo completo
- Contrato
Clinical Research and Regulatory Specialist | MedTech Location: Spain (Remote) Full-time We are looking for a motivated junior professional who wants to develop their career in the MedTech and IVD sector. As a Clinical Research and Regulatory Specialist , you will support clinical research activities, scientific and medical ...
- Remoto
- Tiempo completo
- Contrato
Clinical Research and Regulatory Specialist | MedTech Location: Spain (Remote) Full-time We are looking for a motivated junior professional who wants to develop their career in the MedTech and IVD sector. As a Clinical Research and Regulatory Specialist , you will support clinical research activities, scientific and medical ...
Spain, Alacante
Ver vacante