Site Care Partner - FSP - Spain

Parexel; Salamanca; A distancia; EUR 40.000 - 80.000; Jornada completa

Descripción de la vacante

An established industry player is seeking a Site Care Partner to ensure quality and patient safety at investigative sites. This role involves being the primary contact for clients, overseeing site start-up activities, and maintaining strong relationships with investigators. With a focus on clinical trial methodology and project management, you will contribute to the success of vital clinical studies. The position offers exciting challenges while allowing for a balanced work-life dynamic, making it an ideal opportunity for dedicated professionals in the healthcare sector.

Formación

• 5+ years of clinical research or quality management experience.
• Strong knowledge of clinical development processes and monitoring.

Responsabilidades

• Act as the main client point of contact for investigative sites.
• Ensure site quality and patient safety throughout the study lifecycle.

Conocimientos

Clinical Trial Methodology

Site Management

Project Management

Quality Assurance

Networking and Relationship Building

Multilingual Skills

Educación

BS/BSc/MS/MSc in Healthcare

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’s and top 50 pharmaceutical companies, we offer you enormous security and long-term prospects.

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

The most significant aspect of this position is that

• The Site Care Partner I (SCP I) is the “face of the client” and therefore accountable for ensuring that sites receive necessary support and engagement, issues are resolved, and client’s reputation is upheld throughout study lifecycle.
• The SCP I is the main client point of contact for investigative sites; accountable for site start-up activities through activation; accountable for building and retaining investigator site relationships and providing support from site recommendation through the lifecycle of studies; accountable for site level recruitment and operational success, and accountable for safeguarding the quality and patient safety at the investigator site.
• The SCP I contributes to country and site selection activities by proactively collaborating with key stakeholders and providing local intelligence to country outreach surveys, investigator strategies, and client pipeline opportunities under supervision.

From you we expect

• A scientific or technical degree in the healthcare area is preferred along with extensive knowledge of clinical trial methodology.
• In general, candidates for this job would hold the following levels of education / experience : BS / BSc / MS / MSc or equivalent + 5 years of clinical research experience and / or quality management experience.
• Skills in more than one language are an advantage in this role; English is required.
• Solid knowledge of clinical development processes with strong emphasis on monitoring.
• Demonstrated ability to oversee a 3rd party and / or demonstrated ability in Quality Assurance (preferred).
• Site Management / Monitoring (CRA) experience needed.
• Project management experience preferred in the clinical development area.
• Ability to lead, troubleshoot, and influence for delivery.
• Experience implementing centrally designed and developed initiatives on a local basis.
• Demonstrated knowledge of quality and regulatory requirements for applicable countries.
• Demonstrated knowledge of site intelligence at country / cluster level in support of site recommendation.
• Demonstrated knowledge of clinical trial methodology and the drug development process, related to monitoring clinical trials, GCP, Food and Drug Administration (FDA), or country-specific regulatory environment.
• Demonstrated experience in site activation and startup.
• Demonstrated networking and relationship building skills.
• Demonstrated ability to manage projects and cross-functional processes.
• Availability to travel regularly within country and region is required (3–5 visits per month).

For an immediate interview, please contact.

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