20 publicaciones de empleo destacadas de clinical associate en spain (¡Están contratando!)

Clinical Research Associate I - Madrid
Fortrea —Madrid, Madrid provincia
- Jornada completa
- Servicio al cliente
- Inglés
- Investigación
Clinical Research Associate I
PSI CRO —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Investigación
- Microsoft Office
Solicitud rápida
Assistant CRA
Thermo Fisher Scientific —En remoto
- Jornada completa
- Teletrabajo
- Servicio al cliente
- Inglés
- Microsoft Office
Clinical Affairs Associate
iVascular —Sant Vicenç dels Horts, Barcelona provincia
- Español
- Inglés
- Máster
- Flexibilidad horaria
- Oportunidades de crecimiento y desarrollo profesional
Solicitud rápida
Clinical Research Associate I - Barcelona
Fortrea —Barcelona, Barcelona provincia
- Jornada completa
- Servicio al cliente
- Inglés
- Investigación
Clinical Research Associate (CRA)
Rieka Talent —Castelló d'Empúries, Girona provincia
- 60.000 € al año
- Jornada completa
- Trabajo híbrido
- Español
- Inglés
- Investigación
Solicitud rápida
Clinical Business Operations Associate - Portfolio & Operations Support
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Investigación
- Teletrabajo opcional
RESEARCH ASSOCIATE
Eurofins Spain Pharma Services —Fuente Álamo de Murcia, Murcia provincia
- De 22,22 € a 26,20 € al año
- Incorporación inmediata
- Experiencia en laboratorio
- Mantenimiento
- Investigación
Solicitud rápida
Clinical Research Associate 2 - Multi-Sponsor - Based in Barcelona
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Inglés
- Microsoft Office
- Teletrabajo opcional
Clinical Research Associate 2 - CFSP
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Español
- Inglés
- Microsoft Office
- Teletrabajo opcional
Senior Clinical Research Associate 1 - Sponsor dedicated
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Español
- Inglés
- Investigación
- Teletrabajo opcional
Clinical Research Associate
Opis s.r.l. —Madrid, Madrid provincia
- Hasta 48.000 € al año
- Jornada completa
- Inglés
- Microsoft Office
10d
Associate Safety Project Manager
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Ventas
- Investigación
- Project management
- Teletrabajo opcional
9d
Senior Clinical Research Associate
Alira Health —Barcelona, Barcelona provincia
- De 55.000 € a 65.000 € al año
- Jornada completa
- Servicio al cliente
- Inglés
- Investigación
Associate Director, Medical Affairs
Alcon —Cornellà de Llobregat, Barcelona provincia
- Jornada completa
- Doctorado
- Inglés
- Investigación
Study Start Up Associate II
ICON Plc —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Seguro dental
- Seguro oftalmológico
Associate Consultant
Alira Health —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Associate Principal/Principal Qualitative Research, Patient Centered Solutions
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Doctorado
- Inglés
- Investigación
Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Doctorado
- Investigación
- Máster
Associate Director - Clinical Project Management (IQVIA Biotech)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Teletrabajo opcional

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Clinical Research Associate I - Madrid

Fortrea -
Madrid, Madrid provincia

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Detalles del empleo

Jornada completa

Cualificaciones

Investigación clínica
Servicio al cliente
Inglés
Investigación
Sistema operativo Windows
Microsoft Office
Grado

Descripción completa del empleo

Job Overview:

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.
Assist with training, mentoring and development of new employees, e.g., co-monitoring.
Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client contact as assigned.
Perform other duties 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). An equivalent amount of experience can be substituted as appropriate.
Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
Basic knowledge of Regulatory Guidelines.
Basic understanding of the clinical trial process.
Fluent in local office language and in English, both written and verbal.

Experience (Minimum Required):

Six (6) months experience in a related role (e.g., site management, in-house CRA, study coordinator, research nurse, etc.).
Basic 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.

Preferred Qualifications Include:

One (1) or more year's additional experience in a related field (i.e., medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred.
6 months on site monitoring experience.
Ability to maintain confidentiality of data and information during interactions with staff at all levels and across studies and sponsors.
Demonstrated ability to conduct clinical operations activities most effectively and efficiently.
Attention to detail.
Methodical approach to work.
Understanding of medical and clinical research terminology and clinical research processes.
An understanding of the basics of physiology, pharmacology, and medical devices (when applicable).
Understanding of the principles of ICH GCP, ISO 14155 (if applicable) and regulatory requirements.
Good computer literacy with working knowledge of PCs, Windows, and Microsoft Office applications.
Good oral and written internal and external communication. Strong interpersonal team and organizational skills, personal presentation. The ability to communicate effectively in English.
Experience using a clinical trial management system (CTMS).
For medical device positions, experience in providing customer service to device end users.

Learn more about our EEO & Accommodations request here .

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clinical associate empleos en spain

Clinical Research Associate I - Madrid

Clinical Research Associate I

Assistant CRA

Clinical Affairs Associate

Clinical Research Associate I - Barcelona

Clinical Research Associate (CRA)

Clinical Business Operations Associate - Portfolio & Operations Support

RESEARCH ASSOCIATE

Clinical Research Associate 2 - Multi-Sponsor - Based in Barcelona

Clinical Research Associate 2 - CFSP

Senior Clinical Research Associate 1 - Sponsor dedicated

Clinical Research Associate

Associate Safety Project Manager

Senior Clinical Research Associate

Associate Director, Medical Affairs

Study Start Up Associate II

Associate Consultant

Associate Principal/Principal Qualitative Research, Patient Centered Solutions

Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting

Associate Director - Clinical Project Management (IQVIA Biotech)

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