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  • Current: Clinical Trial Site Identification & Selection

Clinical Trial Site Identification & Selection

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Experience Altasciences' comprehensive clinical trial Site Solutions, including enhanced study design, site identification, and patient search and trial site selection. With a global network of over 150 active clinical trial sites, we are uniquely positioned to support enrollment. We leverage extensive data and experience, to place your study where it most makes sense either at one of our clinical sites in North America or at a partner site. When selecting clinical trial sites, we consider regulatory barriers, indication prevalence, and participant availability to ensure the path forward meets your timeline and budget.

Our global network of specialized sites gives you access to a large pool of patient populations, so you can tackle even the most challenging research projects.  

Learn more about our different areas of expertise.

Benefit From Our Extensive Expertise in Clinical tRIAL Site Selection

We have established relationships with a vast network of investigational sites renowned for their high recruitment potential so you can benefit from:

  • a hybrid approach option, where we work with one or more of our clinical sites as well as with a partner site to support specialty arms;
  • access to histories and data for quicker recruitment;
  • close collaboration throughout your project, including during the crucial feasibility assessment stage;
  • identification of prospective participants prior to site selection; and
  • a project manager dedicated to your studies for efficient trial management.
Altasciences has leading expertise in ophthalmic clinical research.
 

TAILORED Clinical TRIAL Site Support

Trial site recommendations are based on a thorough evaluation of feasibility results, study design, protocol design, analysis by key opinion leaders (KOLs), and patient diversity and geographic breadth. 

Site Identification: Our dedicated team identifies potential partner sites that align with your therapeutic area, geographic preference, and specialty population requirements.

Feasibility Assessment: We thoroughly assess the interests and capabilities of potential clinical sites, ensuring their effectiveness in conducting your clinical trials. Moreover, during the proposal stage, physicians who are already enrolling patients in your targeted therapeutic area offer valuable protocol design feedback providing early input and crucial insight that enables us to proactively address potential challenges and streamline the process.

Comprehensive Analysis: Our experts optimize your clinical trial’s success by evaluating the feasibility results and providing recommendations on the number of clinical sites and their locations.

Qualification and Vendor Assessment: Through our rigorous internal standards and quality evaluations, we assess the experience, capabilities, therapeutic breadth, patient diversity, and risk factors of potential clinical sites.

Streamlined Site Selection: We collaborate with you to formally select the best clinical sites for your trial and initiate start-up activities, for a seamless transition.

Budget and Contract Negotiation: We will prepare for you a site budget comparison, and ensure smooth clinical trial agreement negotiations— pre-established Master Clinical Trial Agreements with our top-tier strategic clinical trial site partners, guaranteeing expedited contracting.

Efficient Investigator Grant Payments: For financial peace of mind, we accurately manage your investigator grant payments in a timely fashion.

Effective Site Management: Our experienced project managers oversee clinical trial site operations, ensuring adherence to protocols, on-time enrollment, and delivery of high-quality data.

 

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