Site Care Partner - FSP - Spain

Parexel; La Coruña; A distancia; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

A leading clinical research organization is seeking a Site Care Partner to be the main client point of contact for investigative sites in Spain. The role involves ensuring quality and patient safety at investigator sites, providing necessary engagement, and managing relationships throughout the study lifecycle. The ideal candidate will have a scientific degree, significant clinical research experience, and strong monitoring skills.

Formación

• A scientific or technical degree in healthcare is preferred.
• Typically 5 years of clinical research and/or quality management experience.
• Strong knowledge of clinical development processes.
• Skills in multiple languages are advantageous; English is required.

Responsabilidades

• Ensure sites receive necessary support and engagement.
• Act as the main client contact for investigative sites.
• Contribute to country and site selection activities.

Conocimientos

Clinical trial methodology

Project management

Networking and relationship-building

Site management/monitoring

Quality assurance

Educación

BS/BSc/MS/MSc or equivalent

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 as well as 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 companies 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. ‘Manageable sites, manageable protocols’ is our mantra. Expect professional challenges in inspiring studies, with time for your outside life.

The most significant aspects of this position are:

1. The Site Care Partner I (SCP I) is the “face of the client,” accountable for ensuring sites receive necessary support, engagement, issue resolution, and uphold the client’s reputation throughout the study lifecycle.
2. The SCP I acts as the main client contact for investigative sites, responsible for site startup activities, building and maintaining investigator relationships, supporting site recruitment, operational success, and safeguarding quality and patient safety.
3. The SCP I contributes to country and site selection activities by collaborating with stakeholders and providing local intelligence for outreach surveys, investigator strategies, and pipeline opportunities under supervision.

From you, we expect:

• A scientific or technical degree in healthcare is preferred, with extensive knowledge of clinical trial methodology.
• Typically, candidates hold a BS/BSc/MS/MSc or equivalent plus 5 years of clinical research and/or quality management experience.
• Skills in multiple languages are advantageous; English is required.
• Strong knowledge of clinical development processes with an emphasis on monitoring.
• Ability to oversee third-party activities and demonstrate quality assurance experience (preferred).
• Site management/monitoring (CRA) experience is needed.
• Project management experience in clinical development is preferred.
• Ability to lead, troubleshoot, influence, and deliver results.
• Experience implementing centrally designed initiatives locally.
• Knowledge of quality and regulatory requirements for relevant countries.
• Understanding of site intelligence at country/cluster level to support site recommendations.
• Knowledge of clinical trial methodology, drug development, GCP, FDA, or country-specific regulations.
• Experience in site activation and startup.
• Networking and relationship-building skills.
• Project and process management abilities.
• Availability to travel regularly within the country and region (3–5 visits per month).

For an immediate interview, please contact.

J-18808-Ljbffr