Clinical Trial Site Management

At Celero, we specialise in site management crafted for biotech needs. Combining thorough site selection with streamlined data processes, our experts ensure your clinical studies run seamlessly.

Celero Clinical Trial Site Management

Site Management Services for Biotech Innovators.

At the heart of our services lies an unwavering dedication to excellence in clinical trial site management. By bridging you with esteemed Sites, KOLs, and regulatory bodies, we not only save you valuable time and effort but also enhance the success trajectory of your trials.

Site Identification and Selection

Thanks to our established relationships with prominent Sites and Key Opinion Leaders (KOLs) in our therapeutic area, we efficiently pinpoint the optimal sites for your trial, saving you time and minimizing guesswork.

Site Management and Organisation

With our deep-rooted connections and organisational prowess, we expertly coordinate the multifaceted components of a clinical trial site. Lean on us for a seamless and efficient trial operation.

Patient Recruitment and Retention

Our tried-and-true strategies, bolstered by our network in the therapeutic domain, ensure a steady influx of suitable participants and lower dropout rates for your trial.

Data Management and Quality Assurance

Our robust data management practices safeguard the precision and security of your trial data. With our rigorous quality assurance, rest assured each data point stands up to the highest standards.

Regulatory and EC Compliance

With our established connections to relevant regulatory bodies, we adeptly steer your trial through compliance mazes, ensuring validity and reliability.

Training and Support

Beyond just training, we provide enriched learning experiences leveraging insights from KOLs, ensuring site personnel are equipped with the latest knowledge and best practices.

Inspection and Audit Readiness

Our meticulous preparation ensures your site stands up to scrutiny, enhancing your trial's reputation and reliability.

IP Handling and Accountability

We bring clarity to the intricate process of IP handling, ensuring impeccable management throughout, letting you focus on the trial's core objectives.

Biospecimen Handling, Accountability, and Transport

With stringent protocols, we ensure each biospecimen is treated with the utmost respect, stored aptly, and transported securely.

Global Coverage

Celero Executive team have experience in 80 trials across multiple clinical development phases (P1-P4) in more than 25 countries (APAC, LATAM, MEA, Eurasia, EU, Central & Eastern Europe).

Celero global industry experts

Clinical Trials

Countries

+

Pharmaceutical Experience

years

Clinical Trials

Countries

+

Pharmaceutical Experience

years

Introducing the Celero Way

A pathway to high-quality, cost-controlled, accelerated trials tailored to your needs.

Learn more about The Celero Way or speak to our Clinical Trial Site Management expert.

Celero’s accelerated controlled pathway and timelines

Celero Clinical Trial Site Management Expert

Speak to an Expert

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