Site Identification Specialist

Experteer Italy; Zona Omogenea Milano Nord; Ibrido; EUR 30.000 - 60.000; Tempo pieno

Descrizione del lavoro

Ein innovatives Unternehmen im Bereich der klinischen Forschung sucht einen engagierten Kandidaten mit einem Abschluss in Lebenswissenschaften. In dieser spannenden Rolle sind Sie verantwortlich für die Identifikation und Platzierung neuer klinischer Studien, die Zusammenarbeit mit medizinischen Fachleuten und die Entwicklung von Strategien zur Beschleunigung der Standortidentifikation. Wenn Sie leidenschaftlich an klinischer Forschung interessiert sind und in einem dynamischen Umfeld arbeiten möchten, ist dies die perfekte Gelegenheit für Sie. Werden Sie Teil eines wachsenden Unternehmens, das seine Mitarbeiter schätzt und an der Spitze der Medikamentenentwicklung steht.

Competenze

• Erfahrung in klinischen Studien ist von Vorteil.
• Fähigkeit, unter Druck mehrere Projekte zu managen.

Mansioni

• Identifikation und Platzierung neuer klinischer Studien.
• Erstellung und Pflege einer standortspezifischen Datenbank.

Conoscenze

Kommunikationsfähigkeiten

Zeitmanagement

Multitasking

Engagement mit medizinischen Fachleuten

Formazione

Abschluss in Lebenswissenschaften

Descrizione del lavoro

Company Description

PSI is a leading Contract Research Organization with more than 22 years of experience, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

Hybrid remote/office working arrangement in Milan area

Job Description

The scope of responsibilities will include:

1. Start-up Responsibilities:

• Involvement in in-house and on-site activities related to site identification and new clinical trial placement.
• Engagement in establishing clinical trial collaborations with medical professionals.
• Ensuring comprehensive internal handovers from Feasibility to Operations.
• Defining the optimal site profile for a study and recommending high-quality sites after evaluating their capabilities.
• Reviewing therapeutic indication and study-specific materials prior to contacting sites.
• Creating and maintaining a site identification tracker.
• Regular communication with Project Teams regarding site identification progress, risks, or issues.

Ongoing Project Responsibilities (all phases):

• Creating and maintaining a therapeutic area-specific site database.
• Assisting Project Teams during enrollment by identifying additional sites.
• Developing strategies to accelerate site identification using external databases and networks.
• Training CTAs and CRAs on site engagement and acting as a mentor.
• Participating in business development and regulatory activities as needed.

Qualifications

• Degree in Life Sciences (proven CRA experience is a plus).
• Experience in healthcare settings (hospital, outpatient clinic) is a strong plus.
• Prior experience in Site Identification/Study Start-Up activities is a strong plus.
• Practical experience in clinical trials activities (study coordinator, sub-investigator) is a strong plus.
• Excellent communication and time management skills.
• Ability to multitask under tight deadlines across multiple projects.
• Fluent in English and native Italian.

Additional Information

We seek a clinical trials savvy candidate who excels in building relationships with medical institutions to advance clinical research. If you want to showcase your skills within a growing company that values its people, PSI is the right place. Join us on the forefront of medication development and collaborate with cross-functional experts to drive your startup projects forward.