Clinical Trial Services

Navigate the journey from pre-clinical discovery to Phase I-IV therapeutic trials effortlessly. Our full-service CRO provides clinical trial services, including optimizing trial site selection, recruitment, protocol design, and regulatory strategy. We can help you expedite your therapeutic innovations from conception to meaningful patient outcomes and quality data.

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Our Range of Clinical Trial Services:

Clinical Trial Preparation Support

Elevate your trials with our expert preparation.

Optimize protocols, understand regulatory requirements, select ideal sites, and plan logistics seamlessly for successful clinical trials.

Clinical Trial Close Out Support

Conclude trials effectively with our close out expertise.

Rigorous site visits, thorough data analysis, regulatory compliance, and detailed final study reports for successful trial closure and reporting.

Clinical Trial Management Services

Enhance your trials with active assistance.

Systematic monitoring, streamlined data management, proactive safety reporting, vendor management and oversight, and adaptable protocol strategies for seamless ongoing clinical trial support.

Are you struggling to execute your clinical trial?

Reduce timeline and trial costs by letting our clinical trial services team assist with full program support or specialty services designed to meet your specific needs.

Frequently Asked Questions

Considering which CRO to use is a pivotal decision for any trial? Here are some answers to commonly asked questions about our clinical trial services.

What is the role of a CRO in clinical trials?

The role of a CRO in clinical trials is multifaceted. They play a pivotal role in selecting appropriate trial sites tailored to the therapeutic indication, ensuring a robust patient pool. Strong project management ensures timely execution. Proficiency in regulatory processes and paperwork streamlines compliance. CROs employ clinical experts for protocol design, data monitoring, and analysis, enhancing trial quality and integrity. Overall, CROs facilitate efficient and successful clinical trial outcomes, combining expertise in site selection, project management, regulatory adherence, and clinical science to advance medical research.

What are the key factors to consider when choosing a CRO?

When selecting the right CRO for your trial, key considerations include the ability to customize the scope to project needs for cost-effectiveness and efficiency. Site-centric leaders who possess a deep understanding of local landscapes are crucial for connecting trials with the right sites and patients. Additionally, a concierge service that guides sponsors through the intricate process ensures transparency, reduces risks, and ultimately contributes to a successful clinical trial journey.

What makes Ichor Clinical different from other CROs?

Ichor Clinical stands out through its personalized approach and unwavering commitment to meeting the unique needs of every project, regardless of its size or complexity. Led by highly experienced clinical trialists, we bring a deep understanding of on-site trial operations. Our extensive connections to US clinical trial sites facilitate efficient and targeted patient recruitment. At Ichor Clinical, we offer a premium experience, combining specialized expertise with a personal touch that larger CROs may struggle to match.

Can I run my clinical trial without a CRO?

Certainly, you can run a clinical trial without a CRO, but it comes with significant challenges. CROs provide clinical trial services including expertise in protocol design, regulatory compliance, site selection, data management, and more. They streamline complex processes, enhance efficiency, and reduce risks. Running a trial independently requires a dedicated team with extensive knowledge and resources, which can be costly and time-consuming. Many sponsors opt for CROs to enable successful trial execution while focusing on their core research objectives.