Ip Manager (Qualified European Patent Attorney)

Parexel; Jerez de la Frontera; A distancia; EUR 35.000 - 55.000; Jornada completa

Descripción de la vacante

Join a leading CRO as a Site Care Partner I, managing critical relationships between clients and investigative sites. Work from home in Spain while ensuring quality and compliance in clinical studies. Your expertise in clinical trial methodology and project management will facilitate success in this dynamic role while offering opportunities for professional growth.

Formación

• 5+ years of clinical research or quality management experience.
• Extensive knowledge of clinical development processes.
• Ability to lead and influence for delivery.

Responsabilidades

• Main point of contact for investigative sites, responsible for quality and patient safety.
• Build and retain relationships with sites and oversee study lifecycle.
• Contribute to country and site selection activities.

Conocimientos

Clinical trial methodology

Site Management

Project management

Quality Assurance

Networking

Relationship building

Bilingual skills (English required)

Knowledge of regulatory requirements

Monitoring clinical trials

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’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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