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Clinical Safety Manager

Remote:

Full Remote

Contract:

Full time

Experience:

Mid-level (2-5 years)

Work from:

Netherlands

Offer summary

Qualifications:

Experience in clinical safety management, Knowledge of pharmacovigilance services, Familiarity with safety reporting regulations.

Key responsabilities:

Oversee the Clinical Safety Management process
Act as main contact for sponsors and teams
Collaborate with finance on project setup.
Ensure compliance with safety reporting requirements
Lead safety team meetings and communication.

QPS Holdings, LLC Pharmaceuticals Large https://www.qps.com/

1001 - 5000 Employees

See more QPS Holdings, LLC offers

Job description

QPS Netherlands B.V. in Groningen is part of an international organization and conducts drug research on behalf of international pharmaceutical and biotechnological companies. We are seeking an experienced Clinical Safety Manager to lead and oversee the Safety Management process within clinical trials. In this role, you will be responsible for establishing safety reporting procedures, managing pharmacovigilance services, and serving as the main point of contact for sponsors, clinical teams, and subcontractors.

This remote role may be filled in the US, in Austria or in the Netherlands.

What will you do?

Oversee the entire Clinical Safety Management process for clinical trials
Act as the primary contact for sponsors, clinical project managers, and the QPS Safety Unit team
Collaborate with the finance team to manage project setup, budgeting, and invoicing
Ensure compliance with safety reporting requirements, including Eudravigilance registration
Develop and maintain Clinical Safety Management Plans, safety databases, and related documents
Lead clinical safety team meetings and ensure effective communication with all involved parties

Work Location