Alternatives to Inato

Talview is an AI-powered, end-to-end hiring & proctoring system that unifies the way organizations screen, interview and assess top candidates and learners. It also ensures a simple, engaging experience. Talview makes it easy for customers to manage their resume/chatbot screening, interview schedules, pre-hire assessments online, on-demand & live interviews, behavioral insights, remote proctoring and remote proctoring from anywhere. Our vision is that every person should have the opportunity to reach their full potential academically and professionally. These are the key benefits: * One solution that unifies all your processes * AI-powered intelligence & insights * Flexible solution that can be tailored to your assessment, hiring, and proctoring needs * Talent of all abilities can be candidate-centric * Data security and privacy commitment *Designed for mobile-first users Talview's customers are able to tap into a vast network of talent.

Our mission is to empower leaders to engage the best talent and turn their business dreams into reality. We want them to make a positive impact on the world. Fetcher will help you achieve your vision, whether you want to hire quickly, increase diversity, expand your talent pool, or save time.

The Medidata Clinical Cloud represents our innovative platform designed to revolutionize the clinical trial journey for patients, sponsors, CROs, and research institutions. As the sole comprehensive technology solution focused exclusively on clinical research, the Medidata Clinical Cloud addresses the entire research spectrum from inception to completion. Our platform enables organizations in the life sciences and medical device sectors to reduce development expenses, manage risks effectively, and expedite the introduction of treatments and devices to the marketplace. Whatever selection you make for your clinical trial initiatives, you will benefit from the capabilities of the Medidata Clinical Cloud. At Medidata, we are at the forefront of the digital evolution in clinical research. With the power of artificial intelligence, machine learning, and sophisticated analytics, our platform connects researchers, study coordinators, investigators, and patients, thereby hastening the research process. Additionally, it provides a regulatory-compliant, patient-friendly electronic informed consent solution for clinical trials, ensuring a smoother experience for all parties involved. This integration of advanced technology not only streamlines operations but also enhances the overall quality of clinical research.

Numerous organizations globally rely on IQVIA to accelerate the drug development process, guarantee the safety and quality of products, enhance commercial efficacy, deliver appropriate treatments to patients, and ultimately promote improved health outcomes by facilitating access to and delivery of healthcare. Transform your approach to clinical development by seamlessly integrating data, technology, and analytics to streamline your trials. The outcome? Quicker decision-making and minimized risks, enabling you to provide transformative therapies at a faster pace. With its expertise rooted in data, sophisticated analytics, and deep industry knowledge, IQVIA offers tailored capabilities to clients throughout the healthcare landscape. Stay informed by exploring the latest insights and updates from IQVIA's data scientists, healthcare professionals, researchers, and other industry experts on crucial topics that resonate with your interests. From emerging industry developments to practical applications of our capabilities, a wealth of information awaits you here. Engaging with this content also empowers you to stay ahead in a rapidly evolving healthcare environment.

Leapcure stands at the forefront of patient recruitment and engagement, bridging the gap between clinical trial sponsors and suitable participants. By leveraging cutting-edge technology and innovative methodologies, we aim to boost both trial enrollment and patient results. Our platform simplifies the recruitment process, allowing for the rapid and efficient identification of qualified candidates for clinical trials. Committed to enhancing medical research, Leapcure strives to make clinical trials more inclusive and impactful. We collaborate intimately with both sponsors and participants to ensure seamless and fruitful trial experiences, which play a crucial role in the advancement of new therapies and treatments. Through our efforts, we are not only improving access to clinical trials but also fostering a more efficient pathway for medical breakthroughs.

Longboat is a cloud-based solution designed to support clinical trials, offering an integrated Guided Compliance toolset that assists users consistently throughout the process. By supplying clinical trial site personnel with essential resources, Longboat enables them to concentrate on patient care. Additionally, it allows participants to access vital study details and receive reminders for upcoming visits. The platform facilitates the streamlined management of any amendments to the clinical trial protocol, ensuring a smooth and controlled rollout. Furthermore, it centralizes the secure sharing of regulated documents among sponsors, CROs, and sites, which significantly enhances the startup process and simplifies traditionally labor-intensive tasks for all research stakeholders. Through a unified support platform, all key participants—including clinical operations teams, monitors, site personnel, and trial participants—can access customized content that addresses their individual requirements. This comprehensive approach ensures that site staff are equipped with the necessary tools and resources to remain engaged and compliant while prioritizing the needs of participants. In doing so, Longboat not only improves operational efficiency but also elevates the overall experience for everyone involved in the clinical trial.

Hired works with over 10,000 companies worldwide to efficiently fill open tech roles. Hired offers the Hired Marketplace, Hired Events, Hired Assessments, and more. Our suite of tools, paired with dedicated Customer Success Managers, helps employers save an average of 45 sourcing hours per hire. Hired is ideal for hiring Software Engineers, DevOps, Product Managers, Designers, and other technical roles.

Connect with skilled engineers from across the globe and hire them seamlessly without any added burdens. Instead of spending countless hours on interviews, focus on your projects by reaching out to engineers who have already been thoroughly evaluated. Our extensive talent network covers various regions and nations, as the top engineers may not be located near you. Discover the most suitable engineers from our pool using our unique, data-driven matching algorithm. Our dedicated success team is committed to assisting you from onboarding through to sharing valuable insights and best practices. Start enhancing your engineering team with exceptional global talent today. Just let us know your requirements, and we’ll manage the rest for you. While brilliance exists everywhere, opportunities are not equally accessible. Talented individuals can be found in every corner of the world, but their potential is often constrained by arbitrary factors such as race, gender, and nationality, as well as the complexities of global collaboration. We are here to elevate human potential on a large scale and create a more equitable pathway for talent everywhere.

TriNetX operates as a worldwide health research network that links healthcare institutions with life sciences firms to enhance real-world research and expedite the creation of innovative therapies. Utilizing a self-service platform that adheres to HIPAA, GDPR, and LGPD regulations, TriNetX allows users to tap into federated electronic health records, various datasets, and consulting collaborations. This capability empowers the global research community to enhance protocol design, optimize trial operations, improve safety signal assessments, and amplify the generation of real-world evidence. The network boasts a comprehensive dataset representing over 275 million patients from 150 healthcare organizations across 25 nations, thereby offering a rich resource for research endeavors. Researchers have taken advantage of the TriNetX network to examine upwards of 26,000 protocols and present more than 7,000 clinical trial opportunities to the healthcare members, thereby cutting site identification time for clinical trials by an impressive 50%. In doing so, TriNetX not only fosters collaboration among entities but also catalyzes advancements in medical research and patient care worldwide.

Historically, clinical trials and medical research operated separately from the routine care provided in local healthcare facilities and by individual doctors. Many physicians remained unaware of ongoing research initiatives, leaving patients largely uninformed about studies that could enhance their treatment outcomes or health. Elligo has transformed this landscape by facilitating unprecedented participation in clinical research through access to a vast network of over 150 million patients and their comprehensive data, enabling doctors to present research opportunities to patients who might not otherwise encounter them. Traditional methods of recruiting participants often face challenges, such as the need for patients to travel to specific research sites, which can limit involvement. Moreover, studies indicate that patients are more inclined to participate in research when it is associated with their trusted healthcare provider, underscoring the importance of integrating clinical research into familiar medical environments. This approach not only bridges the gap between research and patient care but also empowers individuals to take part in potentially life-changing medical advancements.

Experience the forefront of eSource, CTMS, and eRegulatory software designed specifically for clinical trial sites. With CRIO’s top-tier electronic source, you can effortlessly capture source data in real-time, drastically cutting down on paper usage by up to 90% while enhancing data quality by 80%. Gain command over your operations through CRIO’s user-friendly Clinical Trial Management System, allowing you to efficiently schedule patients, monitor financials, and optimize recruiting processes. We proudly present cutting-edge electronic regulatory binders, including the innovative first-ever electronic delegation log, all compliant with 21 CFR Part 11 standards. For clinical trial sponsors, you can perform 100% remote monitoring of your sites’ source data and regulatory documents through a secure online portal. Become a part of our extensive network of over 500 clinical research sites worldwide. Our commitment is to facilitate the growth of your business by streamlining your site’s operations, ensuring that your studies can continue smoothly, regardless of whether you're on-site or not. This way, you can focus on what truly matters: advancing your clinical research initiatives.

Mediktor stands out as the most precise AI medical assistant designed for triage and prediagnosis purposes. We conduct real-world clinical trials involving actual patients, ensuring that our AI solution is validated through clinical evidence. Our understanding of your business allows us to tailor our solution to deliver optimal value, aligning seamlessly with your objectives. Over the past decade, we have collaborated with leading health organizations globally. Our award-winning clinical trials yield significant and convincing clinical evidence that sets a new benchmark in the industry. These trials are carried out in real-world settings and are directed by independent researchers who formulate the protocols, collect data, and synthesize the results. Furthermore, our findings are regularly published in top-tier scientific journals, contributing to the broader medical community. Our AI-driven system emulates the questioning style of a physician, ensuring a comprehensive assessment of patient needs. This unique approach not only enhances accuracy but also fosters trust and reliability in digital health solutions.

AcceleTrial™ eliminates uncertainties in identifying and activating clinical trial sites. Our Study Start-up Management System (SSMS) relies on objective data rather than self-reported information. With AcceleTrial™, you gain access to a comprehensive database of thousands of globally ranked and indexed sites, evaluated based on their specific therapeutic expertise, clinical trial experience, and patient data. This system allows for an objective pairing of the most suitable sites worldwide with the relevant data on expertise, experience, and patient demographics for your clinical trials. You can swiftly engage the right sites to commence patient enrollment through AcceleTrial™'s automated “push and pull” functionality, available in multiple languages. The platform simplifies the process of gathering necessary documents with pre-filled templates and enables real-time tracking of activities. You can begin utilizing the system immediately, as it is a cloud-based solution that requires minimal IT infrastructure or training. Moreover, AcceleTrial™ can be seamlessly integrated with CTMS or other existing clinical trial management systems for enhanced efficiency. This ensures a streamlined approach to clinical trial management, allowing researchers to focus on their core objectives.

Letsremotify simplifies and enhances the remote hiring experience for both businesses and exceptional tech professionals. As an innovative talent-sourcing firm powered by AI, letsremotify specializes in providing HR staffing solutions entirely through a remote framework. By leveraging cutting-edge technologies, they connect companies with over 2 million developers globally, covering a wide array of more than 500 technical skills. Their platform is designed to streamline hiring processes, elevate productivity, and secure a competitive advantage in the remote job market, allowing businesses to invest in premier tech talent to meet and exceed their objectives with tailored dedicated teams. Clients enjoy the flexibility to easily recruit a diverse selection of software engineers, with the ability to assemble a global team in just 24 hours, all while benefiting from a two-week free trial. The mission of letsremotify is to transform clients' visions into reality through committed tech teams, driving international success with effective remote hiring strategies. By fostering strong connections between companies and skilled professionals, letsremotify aims not only to fill positions but to build lasting partnerships that fuel innovation and growth.

Choose Curebase for your upcoming study and enjoy enhanced diversity, accelerated enrollment, and improved patient retention. Our innovative methodology enables patients to participate from the comfort of their homes while being supported by community physicians, resulting in quicker, more cost-effective, and inclusive research studies. Curebase's distinct combination of in-house virtual Clinical Research Coordinators (CRCs) and a worldwide network of virtual Principal Investigators (PIs) collaborates seamlessly with local doctors to deliver studies directly to patients, no matter their location. Since many patients reside far from conventional research facilities, our trials effectively bring research into their homes and everyday medical environments, including local physician offices. Curebase's infectious disease trials successfully engage patients through a pioneering model that aligns with their needs, utilizing community healthcare and virtual environments, enabling broader participation in important clinical research. By leveraging technology and local connections, Curebase not only improves accessibility but also enhances the overall research experience for patients and providers alike.

Cloudbyz CTMS is a cloud-based trial management platform natively built on Salesforce Cloud. It is aimed at sponsors, clinical research organizations (CRO), and clinical sites for managing end-to-end clinical trial operations. Designed for clinical research, it expedites implementation and drives user adoption. Cloudbyz CTMS comes with an intuitive, straightforward design that allows for quick deployment. Boasting a rich set of features, Cloudbyz CTMS makes it easy for users to manage all aspects of clinical trials, including sites, enrolment, documents, events, milestones, site visit reports, finances, inventory, etc. The solution benefits are listed below- 1. Secure, reliable & scalable 2. Faster time to value 3. Monitor study progress & risks from planning to close-out 4. Seamless collaboration among sponsors, CROs & sites 5. Improved clinical team efficiency

Enhance human experiences for all individuals in the talent pool, while simultaneously tapping into the skills and potential of your worldwide workforce. Gain access to the insights and analytics you need to address DEI, pipeline issues, hiring predictions, and team dynamics. Foster more meaningful experiences for candidates, employees, and alumni alike. Improve performance and eliminate biases by integrating countless data points related to talent, skills, and potential. Consolidate your global talent data from various sources, including your company, career sites, ATS, and HR systems into one comprehensive source of truth. The competition for talent has reached unprecedented levels, and the hurdles recruiting teams encounter are increasingly intricate. This marks a pivotal moment where we are genuinely merging data, intelligence, and experience to enhance every aspect of the talent lifecycle, enabling you to achieve your business goals—no matter what they are. By embracing this data-driven approach, you can navigate the complexities of talent management with greater ease and effectiveness.

Deep 6 AI revolutionizes the patient enrollment process for clinical trials by changing how researchers pinpoint suitable candidates. By leveraging artificial intelligence and natural language processing, DEEP 6 AI efficiently sifts through both structured and unstructured patient information, enabling the identification of a larger pool of well-matched trial participants in mere minutes instead of the months typically required. The platform collaborates with leading health systems, pharmaceutical companies, and contract research organizations, positioning itself as an essential component of the clinical research ecosystem and significantly hastening the process for patients to access trials. In addition to expediting enrollment, Deep 6 AI’s innovative software evaluates structured data, like ICD-10 codes, alongside unstructured clinical information such as physician notes, pathology reports, and surgical documents that are often difficult to search through. This comprehensive analysis ensures that researchers can quickly find candidates who meet specific criteria, ultimately leading to faster delivery of groundbreaking treatments to those in need.

We create innovative solutions that enhance and strengthen the clinical trial ecosystem. Our platform for Enrollment Performance Management is favored by research sites and relied upon by sponsors. It is utilized by 2,000 research sites in 26 countries and is endorsed by half of the world's top-20 biopharma companies. This enables sites to reduce time spent on repetitive and manual activities, facilitating a smoother patient progression. By minimizing redundant efforts, there are fewer logs, phone calls, and emails required from both sites and sponsors. Sponsors can proactively improve enrollment with immediate access to advanced pre-screening and enrollment metrics. Our remarkably straightforward patient recruitment and enrollment solution is trusted by over 1,800 sites worldwide. Gain access to impactful recruitment and enrollment insights, ensuring clinical trials are conducted faster and with greater predictability. By eliminating unnecessary tasks, sites can refocus their efforts on what truly matters: providing assistance to patients. Effortlessly manage recruitment across all trials, sponsors, or CROs with the ability to input information once and have it directed where it is needed most. This innovative approach not only streamlines the process but also enhances collaboration among all stakeholders involved in clinical trials.

At Genospace, we recognize that the evolution of precision medicine is being propelled by advancements in genomics, yet the challenge of effectively scaling its implementation remains unresolved. Our mission is to bridge this gap. Our innovative platform aims to transform biomedical data into valuable insights that are easily accessible for all, particularly for those actively involved in delivering care. Equip your clinicians and researchers with essential information that empowers them to make well-informed choices while participating in our goal of utilizing intricate molecular data to enhance patient outcomes and speed up the processes of drug development and research. In this context, the significance of large-scale population data for drug discovery and research cannot be overstated. Utilize cohort-driven analyses through the Genospace platform to support your research initiatives. We have a strong focus on clinical trial research, enabling the Genospace platform to seamlessly align fragmented patient information with intricate trial requirements, thus facilitating quicker patient recruitment. Furthermore, our platform is designed to integrate genomic medicine into standard clinical care practices, making it easier than ever to harness the power of genomics in everyday healthcare. Together, we can push the boundaries of what’s possible in patient care and research.

We aim to simplify the hiring process significantly. Let’s take a moment to explore how we can assist you. Gain a comprehensive understanding of each candidate through data-enhanced profiles that reveal insights beyond what a resume offers, including soft skills and personal interests. It’s a familiar notion: Your workforce represents your most valuable resource. Therefore, it’s essential to nurture their potential by providing the necessary tools for their growth and success as they integrate into your organization. Our intuitive talent management platform features a user-friendly dashboard that enables you to discover and connect with outstanding candidates from various sources such as job postings, job boards, social media, and career websites. You can design the necessary forms for job listings, applications, and compliance, and easily share candidate details within your organization. Additionally, establish learning opportunities that align your employees' development aspirations with your broader business objectives. You can also import external content and courses to engage your current staff, monitor their required certifications and training, and ensure your organization remains compliant. This holistic approach not only boosts employee satisfaction but also enhances overall productivity within your team.

Science 37 is a pioneering clinical research organization that focuses on decentralized clinical trials through its innovative Metasite model, which eliminates the need for physical proximity, allowing patients to engage in studies from virtually anywhere. This method significantly broadens accessibility, reaching over 90% of individuals who might be excluded from conventional site-based research, and harnesses the recruiting capabilities equivalent to 20 sites in one location, thereby offering patients the flexibility they desire. The Metasite operates on a proprietary platform that not only streamlines study orchestration but also facilitates the workflow for both patients and research staff, all while efficiently capturing study data without manual reentry. By centralizing personnel, processes, and technologies, this approach guarantees built-in protocol compliance, which leads to enhanced compliance rates and the collection of high-quality data. Science 37's dedicated in-house medical teams, telemedicine investigators, and mobile nursing professionals are well-versed in the conduct of remote trials spanning various therapeutic areas, thus ensuring comprehensive outreach. This commitment to innovative trial methodologies positions Science 37 at the forefront of transforming the landscape of clinical research.

Making recruitment technology human. Through a smart online chat, Sapia’s Smart Interviewer Phai finds your perfect matches and progresses them directly to a video interview for your hiring team to review. Just two stages, and you’ve found the right talent for the job. Some of the biggest and most trusted global brands use Sapia to automate their volume hiring

Clin'form is an adaptable and powerful electronic Clinical Outcome Assessment (eCOA) platform that aims to simplify clinical trials for both patients and research sites, improve data integrity, and speed up processes for research teams. Its versatility allows it to be used across various protocols and demographics, making it suitable for any type of questionnaire—including Patient-Reported Outcomes (PRO), Observer-Reported Outcomes (ObsRO), Clinician-Reported Outcomes (ClinRO), and diaries—while catering to individuals of all ages, from children to the elderly. The platform is designed to handle diverse population sizes, effectively managing studies that involve anywhere from a small group to over 10,000 participants spread across multiple regions worldwide. Clin'form integrates smoothly with other clinical systems to provide an efficient workflow, supporting various data collection methods such as dedicated tablets or smartphones, the patient's personal device, web access on any browser, and in-person interviews. Noteworthy features include an integrated tele-visit option to accommodate unexpected changes and patient engagement tools that promote high levels of compliance. Additionally, Clin'form's user-friendly interface ensures that both researchers and participants can easily navigate the platform, making the clinical trial experience more streamlined and effective.

Protocol First not only connects disparate locations and dismantles barriers in Clinical Research during the pandemic, but its offerings remain valuable during regular times as well. What was once viewed as optional technology has now become essential. Our solutions facilitate ongoing communication, enabling research not just to persist but to thrive and progress at an accelerated pace. Featuring a fully integrated remote monitoring tool equipped with automatic tagging, our system operates seamlessly with any EDC, anytime, and from any location. Protocol First prioritizes the integration of Sites, Sponsors, CROs, and various functional areas to create a cohesive research environment. We provide holistic solutions that tackle the numerous challenges faced in Clinical Research. The foundation of Protocol First is ensuring accuracy and proper placement of your data, which increasingly incorporates AI, NLP, and ML technologies. A critical component of utilizing AI effectively is establishing a robust structure for your data. The suite of software offered by Protocol First guarantees that data flows efficiently from patients to the FDA, maximizing the potential of data science and enhancing the overall research process. As we move forward, our commitment to innovation will continue to evolve, further amplifying our impact in the field.

Leverage early talent as your strategic edge with Headstart, a dedicated recruiting platform designed specifically for campus, graduate, and entry-level hiring teams. Focus on evaluating a candidate's potential rather than their background, ensuring you bring on board individuals who possess the essential skills your organization needs. Implement a fair and contextual assessment process that incorporates psychographic insights alongside conventional screening criteria. Streamline your hiring processes by automating workflows that cover application screening, skill matching, and candidate selection, thereby minimizing the time required to fill positions. Highlight enticing job opportunities and promote your employer brand through a tailored early talent microsite that resonates with potential applicants. Gather pertinent application details seamlessly through a mobile-friendly and user-friendly candidate experience. Advanced machine learning algorithms prioritize candidates based on their suitability for the role, independent of their history. Additionally, facilitate the assessment process by allowing candidates to participate in both online and in-person evaluations without the hassle of cumbersome scheduling logistics. This innovative approach not only enhances candidate engagement but also drives better hiring outcomes for your organization.

Flask Data equips life science research and development teams with timely clinical data and solutions for patient safety. The Flaskdata.io cloud API platform streamlines data collection applications for patients, researchers, site coordinators, connected devices, and pharmaceuticals. Our offerings in data management and safety oversight are designed to mitigate risks related to clinical data integrity, patient well-being, and adherence to protocols. The Flaskdata.io platform is not only automated but also scalable and responsive to the specific requirements of your clinical trials. Flask Data is a tech firm that focuses on clinical data oversight and management. We excel in delivering optimal solutions that ensure the highest quality of clinical data while prioritizing patient safety. Recognizing that there is no universal solution applicable to all clinical trials, we dedicate ourselves to thoroughly understanding your distinctive challenges. Collaborating closely with your team, we strive to create tailored solutions that meet your needs for high-quality clinical data and enhanced patient safety, ultimately driving the success of your research initiatives.

Forget about outreach, job advertisements, and the tedious process of screening resumes. With HireAI, you can effortlessly connect with your top matches from an extensive network of over 250,000 developers worldwide. This innovative approach eliminates hours of searching, allowing you to quickly identify and hire your perfect candidates. HireAI represents a more intelligent method to recruit the best remote developers from around the globe. You can say goodbye to sifting through countless resumes and instead concentrate on the highest-quality applicants. The platform adapts to your preferences, providing increasingly personalized results with each evaluation. Start engaging with vetted, ready-to-interview candidates immediately, as their verified skills and availability can help you bypass initial interviews. Rather than manually sorting through resumes, you can swiftly discover the best candidates tailored to your needs. The system automatically highlights the most relevant profiles, ensuring you don't overlook any qualified individuals. By using consistent criteria for evaluation, you promote fairness and minimize bias in your hiring process. Additionally, streamlining the candidate experience allows you to swiftly find and contact the most qualified prospects. The efficiency of HireAI not only saves time but also enhances the overall hiring experience for both employers and candidates.

Talentis stands out as an innovative recruitment software designed to enhance user experience and minimize tedious data entry tasks. With its self-cleaning data features, you will not only save valuable time but also increase your productivity and streamline your executive search processes by creating broader and more diverse candidate shortlists. Instead of wasting your time reading this blog, take action by booking a demo before you begin your free trial! Unlike most recruitment platforms that focus on candidates already known to the user, Talentis employs a research-driven approach that supports strategic hiring. Every aspect of our executive search software is meticulously crafted to assist search consultants in identifying, engaging, and recruiting top passive talent. Schedule a demo and then explore your trial options! It’s essential to note that executive search operates on a distinct model compared to other recruitment methods, emphasizing a client-driven and project-oriented approach dedicated to finding the ideal candidate for a specific role rather than merely managing applicants or advertising job openings. This proactive strategy is what sets Talentis apart in the competitive recruitment landscape.

Management of clinical data. Comprehensive solution for managing clinical trial information. Easy data entry and creation of CRFs. Support for multi-center complex studies. Data validation and processing is accelerated Multilingual capabilities. Global deployment, cloud-based and on-premise. Clinical researchers understand the importance of reducing time and costs when conducting clinical trials. This is especially true when it comes to the collection, processing, and management of study-specific data. To ensure that the necessary patient data was recorded and sent to the sponsor for analysis and processing, study coordinators used paper Case Report Forms (CRFs). The days of paper CRFs are long gone. The industry now understands that electronic data capture (EDC), systems increase efficiency and improve data quality.

VIPER streamlines the process of screening by automating remote patient identification right at the diagnosis stage and ensuring qualified enrollment. By leveraging artificial intelligence, VIPER efficiently matches patients to precision trials during a critical enrollment period by utilizing lab-agnostic genomic data, electronic medical records (EMR), and pathology information tailored to both the patient and the research requirements. The system employs a specialized matching engine that searches for the most suitable clinical trials corresponding to a patient's specific diagnosis at the moment they receive it. Additionally, through seamless workflow integration, VIPER provides real-time alerts regarding a patient’s eligibility for available trials, ensuring the entire care team is informed during this narrow enrollment timeframe. Furthermore, VIPER features interactive dashboards that offer extensive data mining capabilities, allowing for the aggregation of site and study-level patient data to effectively meet study key performance indicators (KPIs). This comprehensive approach not only enhances trial recruitment efficiency but also supports researchers in achieving their goals more effectively.

AiCure Patient Connect™ is a comprehensive set of tools compliant with HIPAA and GDPR, designed within a mobile platform to enhance patient engagement, strengthen the bond between sites and patients, and facilitate a more profound understanding of both individual and population-level disease symptoms, ultimately leading to improved health outcomes and trial results. Additionally, AiCure Data Intelligence serves as a versatile platform for data ingestion and visualization, granting sponsors immediate and predictive insights that enhance visibility into the performance of trials and sites, thereby enabling informed, data-driven decisions to address potential challenges before they can affect study outcomes. The data gathered through AiCure’s secure application can effectively support both safety and efficacy endpoints while offering an all-encompassing perspective on the effects of therapy on patients. Furthermore, AiCure caters to the full range of clinical trials, spanning from conventional site-based studies to decentralized or virtual trials, ensuring flexibility and adaptability in various research contexts. This all-encompassing approach positions AiCure as a leader in the evolution of clinical trial management.

Accelerate your development process with carefully selected remote developers who have been approved by leaders from Facebook, Google, and Stanford, ensuring a standard that meets Silicon Valley expectations. Experience a no-risk trial period of two weeks, during which top-tier developers undertake challenging assessments lasting over eight hours, evaluating their expertise across key technological frameworks, algorithmic coding, systems design, and interpersonal skills suited for remote collaboration. With an acceptance rate of less than 1%, we cater to the unique requirements of ambitious companies by swiftly pairing them with the ideal developer in mere days rather than weeks. Our confidence in the quality of our matches is reflected in our payment structure, where companies only incur costs if they are satisfied after the initial two weeks. Developers receive consistent compensation through Turing, eliminating risk for both parties involved. Begin your journey with no upfront commitments, allowing you to pay as you go while effortlessly scaling your team as needed. This flexible approach empowers companies to adapt quickly to changing project demands.

Studypages serves as an all-in-one clinical trial management software aimed at creating a cohesive experience for participants while optimizing clinical operations. It includes a variety of tools that support participant involvement, site administration, sponsor supervision, effective communication, teamwork, and automation of workflows. By merging these features within a singular platform, Studypages significantly boosts the productivity and effectiveness of clinical research, thereby expediting the advancement of medical breakthroughs. Additionally, this integration helps to ensure that all stakeholders are aligned and informed throughout the research process.

Altis Labs has unveiled Nota, a groundbreaking clinical information platform designed to expedite therapeutic research and development. By harnessing the power of AI, Nota can forecast patient outcomes based on imaging data, allowing sponsors to efficiently prioritize their most promising therapies. This innovative platform empowers researchers to effectively utilize clinical trial imaging data, gain access to predictive imaging biomarkers, and enhance R&D efforts on a larger scale. With Altis’ cloud-based software, which employs advanced deep learning techniques, biopharma companies can integrate detailed outcome predictions at the image, patient, and cohort levels, ultimately refining clinical trial design and boosting confidence in anticipating clinical endpoints. The insights generated by Nota have the potential to drastically shorten development timelines, reduce drug development expenses, and increase the chances of success across various therapeutic areas, paving the way for a new era in clinical research. As the demand for efficient drug development continues to rise, Nota stands out as a vital tool for the biopharmaceutical industry.

Connect with carefully screened engineers, engineering managers, sales professionals, marketers, and various other candidates seeking full-time employment. Our platform pairs you with qualified individuals actively looking for job opportunities. By employing assessments, data analytics, and a human-driven screening approach, we ensure you find the ideal candidates for your needs. We tap into leading job platforms, collaborate with a vast network of recruiters, and engage in targeted outreach to source top talent. While we excel in remote hiring, we are also equipped to assist with filling on-site and flexible positions. Laskie offers comprehensive support in crafting your talent acquisition strategy, managing your recruitment processes, and implementing effective hiring practices to enhance your workforce. Moreover, our commitment to understanding your unique hiring needs allows us to deliver tailored solutions for your organization.

In the realm of clinical research, effective organization is a fundamental component of achieving success. Ensuring that the appropriate resources are utilized at the optimal moment presents its own set of challenges, especially concerning document management within a clinical trial. GRAVITY stands out as a long-standing solution for managing site files and trial master files. We have transformed both types of documents into a user-friendly, coordinated electronic format. This comprehensive package enhances document management by providing a logical and convenient framework. As an integrated eTMF and eISF system, GRAVITY serves as a complete cloud-based electronic Document Management System (DMS), acting as a hub for sponsors, CROs, and sites alike. Furthermore, GRAVITY can also function independently for each individual entity as needed. Once a site is chosen to conduct a clinical trial, the influx of documents begins, and the initial set of critical documents necessitates careful management. GRAVITY features a distinctive capability that allows it to monitor essential document management while also notifying users about any documentation that is nearing expiration, ensuring compliance and efficiency throughout the trial process. This proactive approach not only streamlines operations but also enhances the overall quality of clinical research.

Historically, managing clinical trials at investigator sites involved either the cumbersome task of maintaining numerous shared spreadsheets or investing in costly software that often did not fit the Australian context. MAISi represents a revolutionary shift in this landscape. Originating in 2001 as a data repository for clinical trials at a prominent hospital, MAISi has transformed into an advanced workflow application designed to streamline various functions within research units. Serving as a centralized database, MAISi efficiently organizes information related to studies and the corresponding business units that manage them. This structured approach enhances management decision-making capabilities. Individual staff members within each business unit can access specific data pertaining to their studies, patients, investigators, and study team members, while those with broader access rights, typically Financial Officers and System Administrators, can view comprehensive data across all units. Additionally, this streamlined access promotes collaboration and improves overall operational efficiency.

At micro1, we simplify the process for companies to easily recruit top-notch remote software engineers. When you partner with us, you can relax knowing that you won’t have to deal with the challenges of sourcing elite talent, navigating international employment regulations, or managing benefits. We even offer a one-week free trial for each developer you consider. After bringing on a top-tier engineer, our platform allows you to efficiently oversee your new hire—facilitating tasks such as sending bonuses, tracking their hours, implementing raises, and much more. In today’s remote-first work environment, companies that restrict their engineering teams to local commuting areas risk falling behind in the competitive landscape. Your new engineer will be in direct communication with both you and your organization, and you can seamlessly integrate them into all your company’s channels and tools. It's important to note that while you won't be employing the developer directly, you will be engaging micro1's services. By choosing micro1, you gain a layer of protection and support in dealing with legal, compliance, global compensation, and benefits issues. Ultimately, our approach enables you to focus on your core business while we handle the complexities of remote hiring.

The foundation of effective hiring lies in your career website. Our corporate career platforms are designed to attract and engage top-tier candidates, enabling you to secure the right talent for your organization. A well-crafted career site communicates your identity and the unique offerings of your company. Even established brands must provide compelling reasons for candidates to apply, as the most talented individuals have numerous options to consider. Regardless of whether your employment brand is well-defined or in need of an update, we're eager to assist you in sharing your narrative with potential hires. Candidates are genuinely interested in hearing what you have to offer. Furthermore, implementing enterprise solutions doesn’t have to be a time-consuming endeavor; we utilize our extensive experience from creating numerous career sites to establish a streamlined, efficient process that prioritizes success. By focusing on your unique strengths, we can help you make a lasting impression on prospective employees.

The World's Online Agency Recruitment Marketplace This is not a recruitment agency. It is not a job board. Our B2B exchange allows you to connect with the best specialist agencies around the globe. Ubidy is the first global marketplace that connects the largest employers and the top recruitment agencies around the globe to find the best talent. Ubidy makes it easy to manage agency recruitment with its centralized and real time engagements. Ubidy is a platform that helps service providers and employers build more meaningful business relationships while focusing on delivery.

Shortly, Vera will curate a collection of resumes from job websites based on the specifications of the open position. Utilizing advanced technology, Vera is capable of posing questions, assessing responses, and even addressing inquiries from candidates herself. During video interviews, she is adept at detecting the emotions of candidates and provides you with recorded sessions. Vera seamlessly integrates with various employment platforms; just input a brief query to find out how many active candidates are available on a specific site. For those candidates who express interest in the position, Vera facilitates an online interview process that can be conducted directly through the browser. You can rest assured that there will be no repeated calls or messages to the same candidate. When searching across multiple job platforms or when uploading her own database, Vera efficiently eliminates any duplicate resumes. She is equipped to handle a diverse range of job openings, including those for cashiers, programmers, drivers, and marketers, all at the same time, maintaining both quality and speed throughout the process. This allows for a more streamlined and effective hiring experience.

Candidates can submit their applications directly through your website via an iframe integration or be redirected from external platforms such as job boards, educational institutions, or partner sites. Gestmax features a multicast advertising module known as Robopost, which connects to numerous job boards globally. Additionally, Gestmax can be integrated with your intranet, enabling internal candidates, including employees and agents, to request mobility opportunities. This system allows managers to articulate their recruitment requirements effectively. Once these requirements are established, they can undergo various customizable validation processes tailored to your organization's needs. The entire workflow is managed from the job definition stage through to the advertisement creation and its subsequent publication, which can be automatically disseminated across your website and key employment partners. Moreover, this functionality empowers you to develop personalized data directories enhanced with visually appealing graphics. The comprehensive nature of this system ensures that your recruitment processes are streamlined and efficient.

Nexxt offers a comprehensive solution for connecting businesses with the ideal candidates at the optimal time and location. By leveraging cutting-edge technology, a vibrant talent ecosystem, and innovative multi-channel recruitment marketing strategies, Nexxt enables organizations to identify their perfect hires effectively. The platform utilizes intricate data provided by job seekers during profile creation, along with behavioral insights, to accurately match users with the most relevant job opportunities. Its proprietary software employs programmatic job advertising, ensuring that job postings reach the most suitable candidates across various platforms. Additionally, it features hiring software that seamlessly incorporates job posting tools, applicant management functionalities, and reporting capabilities to facilitate successful recruitment. You can effortlessly distribute your job postings to leading job boards, allowing our platform to handle the heavy lifting for you. With Nexxt, you can focus on your core business while we streamline your hiring process.

We assist organizations in optimizing their recruitment process for entry-level positions by linking them with candidates and recent graduates who are well-suited to their specific job requirements and corporate culture. Our extensive candidate engagement initiative runs throughout the year, successfully drawing in numerous aspiring professionals annually, while also offering essential coaching, mentorship, and training to ensure they are prepared for their careers from day one. Each week, our dedicated teams meticulously screen, evaluate, and interview a large pool of candidates vying for entry-level jobs, employing a unique methodology grounded in behavioral science research from the University of Minnesota to identify candidates' transferable skills effectively. Thanks to our exceptional matching system, the retention rates of our placements are twice as high as the national average for similar employees, demonstrating the effectiveness of our approach. Ultimately, our goal is to create a seamless transition for candidates into their new roles, ensuring both employers and employees thrive in the workplace.