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Clinical trial manager

Livorno
ICON
Pubblicato il 6 agosto
Descrizione

We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this role, you will oversee the planning, execution, and successful completion of clinical trials, ensuring adherence to timelines, budgets, and regulatory guidelines. As a leader, you will collaborate with cross-functional teams, manage site relationships, and provide strategic guidance to drive clinical trial outcomes.

What you will be doing

* Manage all aspects of clinical trials, ensuring compliance with timelines, budgets, and quality standards.
* Collaborate with teams to establish and implement trial protocols and procedures.
* Build and maintain relationships with investigators and stakeholders.
* Ensure compliance with regulations and ethical guidelines.
* Make decisions on trial design, vendor selection, and risk management.
* Serve as the primary contact for clinical aspects of projects and develop relationships with stakeholders.
* Plan, schedule, and implement clinical project activities, including protocol management, IP management, and investigator payments.
* Drive enrollment to meet contracted timelines.
* Monitor key clinical metrics and ensure they are met.
* Review and approve visit reports, escalate site issues as needed.
* Ensure timely and accurate clinical data entry.
* Contribute to project plans and documentation.
* Work on multinational studies and potentially serve as a Global CTM.
* Document risks and develop mitigation strategies.
* Maintain operational plans for clinical deliverables.
* Ensure TMF is up-to-date and maintained per SOPs.
* Complete close-out activities at trial end.
* Participate in clinical team meetings and communicate study progress.
* Implement quality control activities and monitor quality metrics.
* Maintain confidentiality of information.
* Participate in business development activities.
* Perform additional project management tasks as needed.

Qualifications

* University degree in medicine, science, or equivalent.
* Experience in monitoring and as a CTM.
* Subject matter expertise in the therapeutic area.
* Ability to travel up to 20%.
* Proactive, detail-oriented, and able to manage multiple tasks.
* Proficiency with Veeva Vault and Microsoft Office.
* Good interpersonal skills and ability to work independently.

What ICON can offer you

We prioritize building a diverse culture that rewards high performance and nurtures talent. Our benefits include various leave entitlements, health insurance, retirement plans, and wellness programs. We are committed to inclusion and providing an accessible environment for all candidates.

Visit our careers website to learn more about working at ICON. We are an equal opportunity employer and welcome applications from all qualified candidates, including those requiring accommodations during the application process.

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