Site Care Partner - Fsp - Spain

buscojobs España; Valladolid; A distancia; EUR 35.000 - 50.000; Jornada completa

Descripción de la vacante

Une entreprise leader dans la recherche clinique recherche un Site Care Partner pour soutenir les études cliniques en Espagne. Ce rôle implique la gestion des relations avec les sites d'investigation, la supervision des activités de qualité et la collaboration avec les parties prenantes pour assurer le succès des études. Les candidats doivent avoir un diplôme scientifique et une expérience significative en recherche clinique, ainsi que des compétences en gestion de projet et en leadership.

Formación

• Diplôme scientifique ou technique en santé requis.
• 5 ans d'expérience en recherche clinique ou gestion de la qualité.
• Compétences en anglais requises.

Responsabilidades

• Assurer le soutien et la qualité des sites d'investigation.
• Gérer les activités de démarrage et d'activation des sites.
• Maintenir des relations avec les sites d'investigation.

Conocimientos

Gestion de la qualité

Compétences en leadership

Compétences en réseautage

Compétences en résolution de problèmes

Connaissance des processus de développement clinique

Compétences linguistiques

Educación

Diplôme scientifique ou technique en santé

Descripción del empleo

If you want to be part of a leading CRO and transform scientific discoveries into new treatments, then Parexel FSP challenges you to live up to your potential by joining us at Site Care Partner (SCP), home-based and sponsor dedicated, in Spain. In this role, you will be the main client point of contact for investigative sites and accountable for safeguarding the quality and patient safety at the investigator site.

We are looking for hard-working, talented, high-caliber people. We know that employee satisfaction leads to customer satisfaction, which is the ultimate driver of long-term success.

As the company that conducts vital clinical studies for sponsors, including the world's leading biotech firms and top 50 pharmaceutical companies, we offer you security and long-term prospects.

Our Site Care Partners work from their home office, supporting studies within their country or region. Our mantra is ‘Manageable sites, manageable protocols’. Expect exciting professional challenges in inspiring studies, with time for your outside life.

The most significant aspects of this position are:

1. The SCP I is the “face of the client” and is responsible for ensuring sites receive necessary support, engagement, issue resolution, and maintaining the client’s reputation throughout the study lifecycle.
2. The SCP I is the main client contact for investigative sites.
3. Responsible for site startup activities through activation.
4. Responsible for building and maintaining investigator site relationships and providing support from site recommendation through the study lifecycle.
5. Accountable for site-level recruitment, operational success, and safeguarding quality and patient safety.
6. The SCP I contributes to country and site selection activities by collaborating with stakeholders and providing local intelligence for outreach surveys, investigator strategies, and client pipeline opportunities under supervision.

From you, we expect:

• A scientific or technical degree in healthcare is preferred, with extensive knowledge of clinical trial methodology.
• Candidates typically hold a BS/BSc/MS/MSc or equivalent plus 5 years of clinical research or quality management experience.
• Skills in more than one language are advantageous.
• English language proficiency is required.
• Solid knowledge of clinical development processes with an emphasis on monitoring.
• Ability to oversee third-party activities and/or experience in Quality Assurance (preferred).
• Experience in site management/monitoring (CRA).
• Project management experience in clinical development is preferred.
• Leadership, troubleshooting, and influencing skills for delivery.
• Experience implementing centrally designed initiatives locally.
• Knowledge of quality and regulatory requirements for applicable countries.
• Understanding of site intelligence at country/cluster level.
• Knowledge of clinical trial methodology, GCP, FDA, or country-specific regulations.
• Experience in site activation and startup.
• Networking and relationship-building skills.
• Ability to manage projects and cross-functional processes.
• Availability to travel regularly within the country and region (3–5 visits per month).

For an immediate interview, please contact us.