Systems and methods for collecting location agnostic clinical and non clinical data

A method implemented by a system for smart data collection of a decentralized clinical trial (DCT), wherein the method comprises:

• collecting, by a processor, clinical trial data and non-clinical trial data, from a device associated with a first set of users at a first location, and wherein the device is a wired device, a wireless device, or a Bluetooth device, and wherein the first location is a hospital, a home, or an alternate care facility, and wherein the first set of users comprises a healthcare professional or a patient, and wherein the clinical trial data is data collected for a decentralized clinical trial for a clinical research, a patient care, and wherein the clinical trial data comprises at least a bio-specimen data, an imaging data, a lab analysis data, and wherein the non-clinical trial data comprises a historical data, a contact information, and a patient-doctor interaction data;
• displaying, by the processor, a user selectable graphic element representing a level of pain on a user interface on the device, wherein the level of pain is denoted on a graphical scale comprising a range of the level of pain on the user selectable graphic element, and wherein the range starts with a minimum level of pain and ends with a maximum level of pain;
• receiving, by the processor, at least one of the clinical trial data through a user selection of the level of pain on the graphical scale within the range displayed on the user graphic element, wherein the level of pain is received by the user selection using a slider to select the level of pain on the user graphical element on the user interface;
• transmitting, by the processor, the clinical trial data and the non-clinical trial data collected at the first location to a central hub;
• automatically converting, by the processor, the clinical trial data and the non-clinical trial data to a compliant dataset, wherein the compliant dataset complies with a regulatory standard for the clinical trial data;
• configuring, by the processor, a role-based access to the compliant dataset to a second set of users, wherein the second set of users comprises a sponsor, a data manager, a care provider, the patient, and the healthcare professional;
• providing, by the processor, the compliant dataset with the role-based access in real time to the second set of users;
• facilitating, by the processor, a real time decision making by the second set of users, wherein the sponsor is given real time access to the compliant dataset for decision making and analytics in real time;
• detecting, by the processor, a high-risk data, wherein the high-risk data necessitates a prompt action;
• and
• automatically notifying, by the processor, at least one user of the second set of users upon detecting the high-risk data, thereby enabling further data collection for a decentralized clinical trial.