Clinical Trial Site Relations Coordinator – Milan

Medpace

Milano

In loco

EUR 55.000 - 75.000

Tempo pieno

6 giorni fa
Candidati tra i primi
Generatore di candidature

Una candidatura apposita per questo posto — un curriculum e una lettera di presentazione personalizzati, perfettamente in linea con l'annuncio.

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Descrizione del lavoro

Medpace in Milan, Italy is seeking a Clinical Trial Site Relationship Coordinator to join our Clinical Operations team. This full-time role focuses on pre-award and post-award study feasibilities, building and maintaining relationships with our network of sites, and developing strategies to conduct feasibilities across Europe.

A background in clinical research or CRA experience is preferred, with English fluency and strong organizational skills.

Competenze

  • Bachelor degree in a health-related field.
  • 1+ year site and clinical trials experience.
  • English fluency required; CRA experience is a plus.
  • Knowledge of GCP, drug development and trial operations preferred.
  • Strong communication and organizational skills.
  • Proficient in Microsoft Office applications.

Mansioni

  • Provide ongoing support of sites, identify new business opportunities and feasibility assessments.
  • Develop site contact plans and follow-up strategies.
  • Support feasibility, site selection and study start-up activities.
  • Serve as site relations expert and maintain relationships with networks.
  • Research site landscape and country intelligence related to patient populations.
  • Coordinate site audits and qualification visits as assigned.

Conoscenze

Clinical trials experience
CRA experience
Fluency in English
Organizational skills
Communication skills
Microsoft Office proficiency

Formazione

Bachelor of Science in health-related field

Strumenti

Microsoft Office

Descrizione del lavoro

Medpace in Milan, Italy is seeking a Clinical Trial Site Relationship Coordinator to join our Clinical Operations team. This full-time role focuses on pre-award and post-award study feasibilities, building and maintaining relationships with our network of sites, and developing strategies to conduct feasibilities across Europe.

A background in clinical research or CRA experience is preferred, with English fluency and strong organizational skills.

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