We are seeking a skilled professional to join our team as a Clinical Trials Coordinator. This role plays a critical part in the setup and management of clinical studies, focusing on financial and contractual aspects.
Key Responsibilities:
* Initiate and oversee site start-up activities, including budget development and contract negotiation with investigator sites, vendors, and internal teams.
* Secure fully executed contracts in alignment with project timelines and organizational priorities.
* Support timely site activation and ensure compliance with regional regulations, data privacy standards, and company quality requirements.
To be successful in this role, you will need strong communication, negotiation, and problem-solving skills. You should also have a strong understanding of the clinical development process and site activation requirements.
Required Skills and Qualifications:
* Bachelor's degree in a relevant discipline such as life sciences, healthcare, business, economics, engineering, or project management.
* Minimum of two years' experience in clinical research (CRO, sponsor, or healthcare setting) or in budget and contract negotiation.
* Strong understanding of the clinical development process and site activation requirements.
* Experience working in a compliance-focused or regulated environment.
* Ability to learn and adhere to financial, legal, and organizational policies.
Benefits:
As a Clinical Trials Coordinator, you will have the opportunity to work with a dynamic team and contribute to the success of our organization.
Others:
Fluency in English and Italian is required for this role.