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HomeServicesSite Management

SiteManagement

Efficient site management is essential for clinical trial success. We establish and maintain productive relationships with clinical sites, ensuring operational efficiency, protocol compliance, and high-quality data generation. Being geographically close to our sites allows us to respond quickly, maintain strong engagement, and build the trust necessary for seamless study execution.

Our service includes

Site Initiation and Training

Comprehensive initiation visits, thorough investigator training to ensure readiness for recruitment, protocol execution, and GCP compliance, and continuous support to guarantee sites are fully prepared for patient recruitment and trial execution.

Retraining Programs

Providing refresher training sessions during the study when necessary to maintain protocol adherence and study quality.

Compliance, ongoing Communication and support

Regular communication to support site teams, reinforce protocol and regulatory requirements, and proactively manage queries and documentation throughout the study.

Site Performance

Ongoing tracking of site performance metrics, early identification of deviations, and implementation of targeted actions to maintain enrollment and quality milestones.

At GALSER, we view site management as a core pillar of study success. By working closely and responsively with site teams, we create the optimal environment for operational efficiency, patient engagement, and regulatory excellence.

Faq

Business professional

Feedback from our clients

GALSER team has shown a great mix of professionalism, flexibility/adaptability and profound knowledge of the human research landscape in Switzerland
Big Pharma​
Medical Affairs Associate

01

/05

The GALSER team guided us through the Swiss regulatory process with clear advice and great responsiveness. Their support made the entire submission much easier than we anticipated.
Mid-Size Company​
Director Clinical Operations Europe

02

/05

We were impressed by GALSER’s strong relationships with the study sites and their ability to keep things moving despite the usual challenges. It really helped us stay on track
Big Pharma​
Head of Global Clinical Development

03

/05

Your level of detail and expertise really stand out. It’s been a real pleasure working together!
Start-Up​
CMO

04

/05

A remarkable project leader who managed to deliver a high-quality protocol in a very short time
Swiss University Hospital
Principal Investigator - Initiated Investigator Trial

05

/05

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