Clinical Trials Hub Coordinator Specialist

hace 1 mes


Madrid, Madrid, España Chubb - Disabled A tiempo completo

Overview

Chubb is seeking an experienced Clinical Trials Hub Coordinator to join our team. As a key member of our global operations, you will play a crucial role in coordinating the downstream processing of clinical trials.

About the Role

The ideal candidate will have excellent communication and organizational skills, with the ability to manage multiple tasks and priorities effectively. You will work closely with underwriters, affiliates, and other stakeholders to ensure seamless coordination of clinical trial programs.

Key Responsibilities

  • Coordinate the downstream processing of clinical trials business, including data completion and hand-off sheets.
  • Manage inquiries from brokers or clients on their clinical trials programs.
  • Aid underwriters in completing the Clinical Trials underwriting process and maintaining accurate policy records.
  • Provide expert knowledge on clinical trials for underwriters and facilitate communication with regional leaders.
  • Support underwriters by providing underwriting, regulatory, and compliance information, and advice on program structure.
  • Ensure CHUBB's Service Standards are met and exceeded in the implementation of multinational clinical trial programs.
  • Liaise with Affiliates and the Shared Service Centre to ensure timely and high-quality administrative activities.
  • Drive development of more efficient processes and support underwriters in solving IT issues.

What We Offer

We offer a competitive salary range of $80,000 - $110,000 per annum, depending on experience, plus benefits including:

  • 30+ days of vacation per year
  • 2 days working from home option + additional flexible days
  • Working from home allowance
  • Entry time flexibility
  • Life and accident insurance
  • Pension plan
  • Gympass
  • Comprehensive Learning & Development offer

Requirements

To be successful in this role, you will need:

  • Excellent communication and organizational skills
  • Ability to manage multiple tasks and priorities effectively
  • Experience in clinical trials or a related field
  • Knowledge of underwriting, regulatory, and compliance procedures
  • Strong analytical and problem-solving skills

Location

This role is based at Chubb's global headquarters, where you will work collaboratively with a diverse team of professionals.



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