CLINICAL RESEARCH ASSOCIATE
Sant Cugat del Valles, ES
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¿Te gustaría unirte a un equipo internacional que trabaja para mejorar el futuro del sector de la salud? ¿Quieres contribuir a mejorar la vida de millones de personas? Grifols es una compañía global del sector de la salud que desde 1909 mejora la salud y el bienestar de las personas en todo el mundo. Somos líderes en medicamentos hemoderivados y medicina transfusional y desarrollamos, producimos y comercializamos medicamentos, soluciones y servicios innovadores en más de 110 países y regiones. |
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We believe that diversity adds value to our business, our teams and our culture. We are committed to equal employment opportunities that foster an inclusive environment.
Mission
Provides support in the oversight and management of vendors. Conducts review of clinical data to ensure site adherence to applicable regulatory requirements, ICH/GCP Guidelines, company SOPs, and study protocols. Assist in the clinical trial management to ensure timelines and metrics are met and maintained throughout the study.
What your responsibilities will be
- Supports the Program Manager in clinical trial management
- Assists with vendor oversight (CRO, IVRS, and supports trial planning and execution)
- Contributes to the creation and tracking of study documents and maintains CTMS data.
- Supports audits, document reconciliation, and resolution of monitoring/TMF findings with QA.
- Helps coordinate study meetings (Kick-Off, Investigator) and prepares agendas/minutes.
- Assists in training CROs, vendors, and site staff on study procedures and SOPs.
- Contributes to Sponsor oversight of the clinical monitoring
- Verifying that investigational product (IP) procedures at the site are conducted in alignment with applicable study documents and regulatory requirements.
- Conducts and supports site visits (selection, initiation, monitoring, close-out) and addresses site issues.
- Oversees site performance to ensure protocol compliance, patient safety, and study timelines.
- Reviews monitoring reports, supports TMF review, and ensures documentation completeness.
- Trains monitors and assists in resolving issues identified during site monitoring.
- Supports regulatory document review and site activation readiness.
- Coordinates with Clinical Supply Chain and resolve queries and supports IP and safety processes.
- Carries out in-house clinical monitoring activities.
- Performs/co-monitors site visits and documents outcomes per SOPs and guidelines.
- Supports site selection through feasibility assessments and pre-study visits.
- Manages clinical supplies and drug accountability at sites.
- Ensures data integrity through review of study documents and query resolution.
- Identifies site issues, initiates corrective actions, and follows up.
- Supports site payments and overall site engagement.
Who you are
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions).
- You have a Bachelor’s Degree in Health Sciences or related field.
- Minimum of 2 years of experience in clinical research, preferably in trial coordination, monitoring, or CRO/vendor management.
- Strong organizational and communication skills, with the ability to translate complex clinical data into clear and actionable insights.
- Proactive, solution-oriented mindset with the ability to work independently and collaboratively in cross-functional teams.
- Advanced level of English
What we offer
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.com. If 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.
Flexibility for U Program: Hybrid Model
Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).
Benefits package
Contract of Employment: Temporary position
Location: Sant Cugat del Vallès.
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Ubicación: SPAIN : España : Sant Cugat del Valles:[[cust_building]]