Cargando...

QA Specialist QC Monitoring

Ubicación: 

Sant Cugat del Valles, ES

Tipo de Contrato:  Indefinido tiempo completo
Área:  Calidad
Número de solicitud de puesto:  131381
Grifols | Desarrollo del talento

Grifols es una compañía global cuya misión es mejorar la salud y el bienestar de las personas. Nuestras tres divisiones -Bioscience, Diagnostic y Hospital- desarrollan, producen y comercializan productos y servicios innovadores para los profesionales médicos en más de 100 países.

 

Nos comprometemos a fomentar el aprendizaje continuo y el desarrollo y crecimiento profesional. Como empresa dedicada a mejorar la salud y el bienestar de las personas, buscamos profesionales con talento que quieran unirse a una compañía global, en un ambiente de trabajo estimulante y gratificante.

Grifols is a global healthcare company with more than 75 years of history improving the health and well-being of people around the world. We produce essential plasma medicines for patients and provide hospitals, pharmacies, and healthcare professionals with tools, information, and services they need to efficiently deliver expert medical care. We are present in more than 100 countries, with global headquarters in Barcelona, Spain, where the company was founded.

As a company committed to serving people, we seek to hire and retain the very best employees.

Our day-today corporate culture reflects the Grifols Spirit, which is defined by our Values.

 

From Clinical Quality Assurance department we are looking for a QA Specialist QC Monitoring.

 

YOUR TASK AND RESPONSABILITIES

  •  You are going to provide sponsor quality oversight of clinical activities ensuring that procedures related to investigators, vendors and facilities are conducted in accordance with the protocol, Clinical Monitoring Plan and other study plans, Standard Operating Procedures, ICH Guideline for Good Clinical Practice and regulatory requirements.
  • To conduct quality control activities in clinical studies.
  • To assist in the development and update of the internal procedures.
  • To ensure communication to senior management of any critical non-compliance risk and the implementation of corrective and preventive actions.

  

WHO YOU ARE

  •  You have a Life Sciences Degree or similar.
  • Your experience is minimum of 5 years in a similar role or provide experience in Clinical Trials.
  • You have a native level of Spanish and Advanced in English.
  • You have Ability and willingness to travel occasionally.
  • You have Ability to work both in a team and independently.
  • You have Ability to meet deadlines, multitasks, and prioritize based on study needs.
  • You have Ability to works on assignments with a diverse scope.
  • You have Ability to work with a very limited direct supervision.
  • Your knowledge of ICH/GCP Guideline and regulatory requirements.
  • Your knowledge of electronic data capture (EDC) systems and electronic trial master file (eTMF) systems.
  • Your advanced knowledge of monitoring activities/procedures.
  • Your Advanced knowledge of medical terminology.
  • Your Advanced knowledge of the therapeutic areas assigned.
  • Rour Advanced knowledge of pharmacovigilance procedures.
  • Routinely demonstrates mastery of technical skills

 

WHAT WE OFFER

  • Location : Sant Cugat 
  • Contract of Employment: Permanent position

 

It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.

 

Information about Grifols is available at www.grifols.comIt you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply!

We look forward to receiving your application!

Grifols is an equal opportunity employer.

 

    Location: Sant Cugat del Vallès

    Conócenos un poco más