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.
Benefit From Our Extensive Expertise in Clinical 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.
TAILORED Clinical Site Support
Site recommendations are based on a thorough evaluation of feasibility results, 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 interest and capabilities of potential sites, ensuring their effectiveness in conducting your trial. 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 trial’s success by evaluating the feasibility results and providing recommendations on the number of 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 sites.
Streamlined Site Selection: We collaborate with you to formally select the best 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 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 site operations, ensuring adherence to protocols, on-time enrollment, and delivery of high-quality data.
EXPLORE MORE OF ALTASCIENCES' CLINICAL SERVICES
Advancing your drug candidate smoothly to proof of concept is what we do best.