16 publicaciones de empleo destacadas de clinical trial associate en barcelona barcelona provincia (¡Están contratando!)

Clinical Research Associate II - Barcelona
Fortrea —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Inglés
- Grado
1d
Clinical Research Associate 2 - CFSP
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Inglés
- Microsoft Office
- Teletrabajo opcional
Clinical Research Associate 2 - Multi-Sponsor - Based in Barcelona
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Inglés
- Microsoft Office
- Teletrabajo opcional
Senior Clinical Research Associate
Alira Health —Barcelona, Barcelona provincia
- De 55.000 € a 65.000 € al año
- Jornada completa
- Servicio al cliente
- Inglés
- Investigación
Clinical Research Associate 2 - IQVIA Biotech
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Grado
- Gestión del tiempo
- Teletrabajo opcional
Associate Clinical Programmer - Clinical Data Operations
Novartis —Barcelona, Barcelona provincia
- De 27.900 € a 51.900 € al año
- Jornada completa
- Informática
- Inglés
- Investigación
Associate Clinical Programmer - Clinical Study Data, Risk based Quality Management & Monitoring
Novartis —Barcelona, Barcelona provincia
- De 27.900 € a 51.900 € al año
- Jornada completa
- Informática
- SQL
- Grado
Global Study Associate Director - Single Sponsor dedicated
IQVIA —Barcelona, Barcelona provincia
- De 225.500 € a 418.600 € al año
- Jornada completa
- Investigación
- Project management
- Grado
- Teletrabajo opcional
1d
Associate Director, Global Health Economics and Outcomes Research Analytics
Alexion Pharmaceuticals,Inc. —Barcelona, Barcelona provincia
- Doctorado
- Informática
- Máster
Associate Principal/Principal Qualitative Research, Patient Centered Solutions
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Doctorado
- Inglés
- Investigación
HTA & Modelling Science Associate Director
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Oficina
- Grado
Senior Project Manager / Associate Project Management Director
Optimapharm d.o.o. —Barcelona, Barcelona provincia
- De 80.000 € a 100.000 € al año
- Jornada completa
- Teletrabajo
- Inglés
- Investigación
- Máster
Associate Director, Biostatistics - IQVIA Biotech (m/w/d)
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Doctorado
- Investigación
- Máster
- Teletrabajo opcional
3d
Expert Clinical Programmer - Clinical Study Data, Risk based Quality Management & Monitoring
Novartis —Barcelona, Barcelona provincia
- De 36.100 € a 67.100 € al año
- Jornada completa
- Informática
- SQL
- Project management
Associate Director-Biostatistics
RTI International —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Doctorado
- Investigación
- Oficina
7d
Statistical Programming Associate Director
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Informática
- Liderazgo

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Clinical Research Associate 2 - CFSP
IQVIA —Barcelona, Barcelona provincia
Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on…

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Clinical Research Associate II - Barcelona

Fortrea -
Barcelona, Barcelona provincia

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Detalles del empleo

Jornada completa
Hace 1 día

Cualificaciones

Español
Inglés
Grado

Descripción completa del empleo

Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned.

Summary of Responsibilities:

Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned.
Responsible for all aspects of site management as prescribed in the project plans.
General On-Site Monitoring Responsibilities.
Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study.
Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements.
Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review.
Monitor data for missing or implausible data.
Ensure the resources of the Sponsor and Fortrea are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Fortrea travel policy.
Ensure audit readiness at the site level.
Travel, including air travel, may be required and is an essential function of the job.
Prepare accurate and timely trip reports.
Interact with internal work groups to evaluate needs, resources, and timelines.
Act as contact for clinical trial supplies and other suppliers (vendors) as assigned.
Responsible for all aspects of registry management as prescribed in the project plans.
Undertake feasibility work when requested.
Participate in and follow-up on Quality Control Visits (QC) when requested.
Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor as assigned 18) Assist Senior CRA with managing investigator site budgets.
Track and follow-up on Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs.
Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management.

Qualifications (Minimum Required):

University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure).
Thorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements.
Fluent in Spanish and in English, both written and verbal.
Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Experience (Minimum Required):

Minimum 2 years of experience as independent monitor .
Previous monitoring experience in Oncology clinical trials is highly preferred.
B asic understanding of Regulatory Guidelines.
Ability to work within a project team.
Good planning, organization, and problem-solving skills.
Good computer skills with good working knowledge of a range of computer packages.
Works efficiently and effectively in a matrix environment.
Valid Driver's License

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