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TIME gives you access to a network of providers and patients to accelerate enrollment in your clinical trials.
Contact UsOpen trial sites consistently and reliably within an average of 10 business days, compared to the industry average of 8 months.
Read case studyIdentify eligible patients with the highest likelihood of enrolling in your trial with our enhanced trial matching services — a unique combination of software, machine learning, and clinical experts.
Leverage our pre-qualification process and team of experienced physicians, nurses, and research coordinators to get the most out of your participation in TIME.
The TIME program complements your traditional trial sites by bringing your study to patients faster, in locations where they already receive care. We do this through enhanced patient matching, rapid site activation, and site engagement initiatives.
A pre-qualified site is activated just-in-time when a subject is ready to join your study. Through a series of streamlined activities and agreements, TIME can help you activate new sites for your trial within an average of 10 business days. Our vast TIME network of academic medical centers and community-based sites continues to grow, and enables trial access for all patients — regardless of location.
200+
provider networks and research institutions signed up for the program
2,800+
oncologists are fully enrolled
160+
biopharma partnerships
200+
clinical trials have been signed up for the program
20K+
patients identified for potential enrollment in clinical trials
10
business days on average to activate a new site
TIME uses a comprehensive approach to identify patients who are eligible for your trial.
Clearly defined inclusion/exclusion criteria and curated patient data allow Tempus Nurse Navigators to precisely assess patient eligibility within a single tool.
Our checklist user interface provides transparency into the trial matching logic and guides Nurse Navigators through a secondary review.
Data shown is not real patient data.
Our patient tracker makes it easy for TIME trial sites to monitor patients and collaborate with Tempus throughout the screening and pre-enrollment process.
Data shown is not real patient data.
TIME sites are consistently activated within an average of 10 business days. Research standardization and on-site support enables operational efficiency to make this possible.
TIME increases awareness of your study through ongoing clinical outreach with clinical trial sites.