Sponsor Dedicated Clinical Project Coordinator Based in Switzerland

Vor 6 Tagen

Zürich, Schweiz Fortrea Vollzeit

Imagine your expertise making waves in groundbreaking clinical trials
- where every day brings the chance to change lives. We are searching for an exceptional Clinical Project Coordinator, ready to work alongside some of the brightest minds in the field.
- This role is for upcoming future opportunities that may arise at Fortrea. _

**Responsibilities**:

- **Support Global Study Operations**: Assist the global study team with delegated tasks, ensuring compliance with GCP, regulatory standards, and sponsor's internal procedures.
- ** Coordinate Study Logistics & Communication**: Manage study documentation, internal and external communications, training materials, and vendor system access across various platforms.
- ** Maintain Study Tracking Systems**: Oversee and update operational tools (e.g., CTMS, eTMF...), track study progress, and generate reports for study leadership.
- ** Organize Meetings & Events**: Lead logístical coordination for internal and external meetings, including investigator meetings, vendor kick-offs, and training sessions.
- ** Ensure Documentation Quality**: Maintain and audit the Trial Master File (eTMF) for completeness and compliance, supporting regulatory submissions.
- ** Support Outsourced Studies**: Act as a liaison between Medical Affairs, CROs, and internal teams.
- ** Drive Process Improvement**: Contribute to departmental initiatives and special projects aimed at enhancing operational efficiency and quality.

**Requirements**:

- University or college degree, preferably in a healthcare or scientific field; relevant clinical research experience may substitute for formal education.
- Fluent in German and English, both written and verbal (French and/or Italian may be a plus)
- 2-3 years of experience in clinical research, with at least 1-2 years in a project management setting.
- Familiarity with clinical trial processes, protocol designs, study procedures, and project timelines.
- Knowledge of GCP/ICH Guidelines and applicable regulatory authority requirements.

**What we Offer**
- ** Career Growth & Development**: Gain hands-on experience in clinical research with opportunities for professional training and career advancement.
- ** Supportive Work Environment**: Be part of a collaborative and dynamic team, working alongside experienced professionals in a sponsor-dedicated role.
- ** Competitive Benefits Package** that also involve flexible working arrangements, access to wellness programs and feel included by joining Employees Resource Groups to build relationships and expand your network.

Join us in shaping the future of clinical research while building a fulfilling career

LI-GQ1

Learn more about our EEO & Accommodations request here.

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