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Patient Recruitment, rather than being a single activity is a host of responsibilities that range from protocol development and study feasibility to site selection and various activities from first-patient-in to last-patient-in. Patient recruitment and enrollment is a variable that can jeopardize drug development timeline. Delays could be caused by: Patients and investigators who are unaware of study opportunities, Difficulty accessing patients in non-traditional regions, competing protocols limiting the number of patients available to participate in studies. For successful completion of clinical studies and clinical trials goal should be to find the right patients, at the right time, to support delivery of effective study results. Informatics tools and media-based recruitment methods to identify and reach appropriate patients and investigators. The system should be able to select broad pools of quality, prescreened patients, a proven, highly efficient enrollment process, and a proper call center. Streamlining recruiting, screening and enrolling processes to Clinical Investigator. Issues with patient recruitment and enrollment are the primary causes for missing clinical trial timelines. The costs associated with patient recruitment delays are not only high, but difficult to anticipate and control. Consistently updated regulations, newly developed media by which to attract patients and investigators, and selecting appropriate service providers for recruitment all play a role in patient recruitment dynamics. There are two primary ways clinical trial managers can find patients to fill their trials: A patient can be pulled into clinical trials by way of their physician who happens to be a principal investigator for a clinical study. This method relies on the patient population of the physician/ site and the efforts of the investigator and their staff in identifying potential patients and enrolling them in the study. These types of recruitment efforts may be aided by in-practice recruiting tools (e.g. table tents, posters) and by paper or EMR chart reviews or be pushed towards clinical trials. Using this method, patients are encouraged to find a particular investigator or site, typically one they may have little or no previous contact with. Pushing patients towards clinical trials may be done through media outlets such as television, social media, billboards, radio advertisements, email targeting, etc. In addition, outside services like patient networks and patient recruitment companies identify patients and attempt to push them towards clinical trials. Primary and secondary research is conducted to uncover some of the fundamental trends in patient recruitment within the clinical trial space. Additionally, through primary research efforts, data is gathered that provide a high-level understanding of the patient recruitment outsourcing market – including both the current state of that market and future projections. Overall, the use of standalone patient recruitment service companies and patient networks is relatively low, but their penetration is expected to increase. One thing that long-time watchers of the pharmaceutical industry will know is that sponsor companies often have a hard time changing. The industry is highly regulated and processes have been built around these regulations. Taking different approaches takes time to implement. Achieving last-patient-in milestones requires extensive planning and hard data, supported by utilizing a big data engine combined with the voice of the patient, the voice of investigator intelligent and real-life scenario planning and real-life study simulations to identify, quantify and visualize the best possible development strategy. Because there are always obstacles and detours on the road to trial fulfillment, a proactive, contingency-based escalation process is to be built with pre-defined trigger points. One should possess comprehensive abilities to forecast, monitor, and manage patient recruitment, along with providing complete range of patient outreach and site-support services such as information, training, and other forms of assistance designed to minimize delays that can add millions of dollars to the cost of clinical trials. Clinical trial recruitment has to be more precise, predictable, and efficient which can be achieved by using real-world data and analytics to develop more precise study plans and select sites based on target patient population density. These new data-driven tools maximize site recruitment and activate alternative recruitment channels resulting in trial recruitment to be more efficient and predictable. Predicting enrollment more accurately, using a next generation of clinical development approach to develop site-level recruitment plans based on target population density. Increase the number of patients per site and improve patient retention rates with protocol-specific strategies for patient engagement and specialized recruitment resources, such as Clinical Trial Educators. Where needed, leverage precise online targeting to locate interested patients with cost-effective outreach strategies. Avoid delays through fully integrated data-driven recruitment tools and proactive site support. Clinical trial management service provider to the pharmaceutical, biotechnology and medical device industries and to Academia/Government constantly requires clinical trial investigators who enjoy remaining close to medical science and to the development of new medicines. Clinical trial investigators play a crucial role in the development of new medicines and with the ever expanding number of clinical trials and non-interventional research studies being conducted. Clinical studies or clinical trial patient recruitment should involve Patient-Centered Sciences, emphasising patient engagement enrolling participants for your study with a large Active Recruiting Database.

PATIENT RECRUITMENT
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Celerion

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ERT

Elligo Health Research

Evidera

Factory CRO

KAI Research

Mapi Group

Nutrasource

PAREXEL International Corporation

Quorum Review, Inc.

Quotient Sciences

Reliance Clinical Testing Services, Inc

Spaulding Clinical, LLC

SubjectWell

Synexus Limited

TFS International AB

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Virtual BoothTransforming Drug Development with Science & Innovation.

Rapid Subject Recruitment

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Quotient has the experience & expertise to seamlessly deliver your studies with the highest quality service & speed to clinical data. If you need a complete service including data analysis, subject recruitment, medical writing, Quotient is your answer.

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Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

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Boost Patient Enrollment

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Traditional methods of increasing enrollment are expensive and inefficient. SubjectWell’s recruitment marketplace helps you find the right candidates faster so you can stay on schedule, avoid risky spending on recruitment, and get to market faster.

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Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

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Find Patients & Fill Trials

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Our team focuses on narrowing the gap between patients and clinical research by reaching out to physicians and their patients and helping them participate in clinical trials.

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Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

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Enrolling Participants for Your Study

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When you place a study with Spaulding Clinical Research you have access to a team of recruitment experts, who are dedicated to enrolling participants for your study. Our recruitment metrics show that our team delivers and they do it on budget.

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Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

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Best in Class Patient Retention

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We develop study-specific retention plans when needed but our main retention strategy for all studies is to maintain close interaction with both patients and the primary care provider. We ensure patients feel valued, are kept informed.

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Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

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Patient-Centered Sciences

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Patient-Centered Sciences combined services establish Mapi as the clear industry leader in supporting patients or their caregivers, and offer proven results for accelerated drug development, improved recruitment, increased patient engagement, excellence in patient-reported data, and minimized

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Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

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Safety-in-Use (SIU) Studies

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To determine the safety of topical products, RCTS provides a range of clinical testing procedures, including a broad range of in-use and patch studies. Determining product safety under normal or exaggerated use conditions.

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Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

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Patient Engagement Plans

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The Patient Engagement Plan places the patient at the centre of the clinical trial’s preparation and management. Each plan is different, tailored to the specific circumstances of the patient community within the chosen country.

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Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

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Surpass Your Enrollment Targets

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SubjectWell continuously engages the 96% of Americans who have never participated in a clinical trial. We are already talking to patients near your site who are looking for studies and have relevant health conditions.

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Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

ERT

  • FDA

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Patient Engagement

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Optimize study power and achieve maximum enrollment, retention and compliance with our patient-centric design, tailored patient outreach and automated BYOD technology.

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Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

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Patient Recruitment & Clinical Site Partnersh...

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We understand potential obstacles to recruitment and recognize the importance of a well-outlined recruitment and retention plan developed in conjunction with the study protocol.

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Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

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Recruitment that’s Different

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Traditional trial recruitment methods look for patients with a particular health condition who happen to live close to a specific clinical site. This is targeting a needle in a haystack. At SubjectWell, we engage the entire haystack – the 96% of people who have never participated in clinical

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Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

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Active Recruiting Database

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On average, Celerion screens more than 2,300 subjects per month. This success rate is attributed to our experienced staff, our extensive recruiting efforts and our ability to understand both the study requirements and the local subject pool for each of our clinical facilities.

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Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

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Informed Consent for the 21st Century

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Imagine an eConsent solution that improves compliance and consent accuracy and provides an IRB-integrated process that activates studies in days instead of weeks. Q Consent is the future of electronic informed consent and it’s available now for your research studies.

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Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

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Patient-Centered Research

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Evidera’s patient-centered researchers represent a unique combination of scientific disciplines, including psychometrics, economics, decision analysis, epidemiology, biostatistics, psychology and public health.

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Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

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Clinical Trial Patient Recruitment

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PAREXEL leverages over 30 years of clinical trials experience with a data-driven approach that integrates all drivers of effective clinical trial patient recruitment.

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Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

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Patient Inclusion & 24 Hours Randomization

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We are counted on for swift and reliable clinical medicalndevice/IVD services by companies and clients from everyncorner of the globe.

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Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

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Clinical Sourcing & Staffing

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With a large global network of talented clinical research professionals and vast industry expertise, DZS provides recruiting services across a range of clinical development positions and locations.

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Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

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Investigator Recruitment & Site Management

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At TFS we strive to ensure costs are kept within the budget using our in-depth knowledge of international and local regulatory requirements and our network of global investigators to ensure that the trial objectives will be met on time.

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Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

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Participant Enrollment

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Participant enrollment is often the single largest cause of delays in clinical research and often accounts for one quarter of the clinical program timeline. Our team expedites this process by taking a strategic approach to clinical trial recruitment.

- Directory Listing

Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

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Patient Recruitment Services

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TFS offers a proven process for rapid patient recruitment without compromising results. With access to a worldwide network of KOLs and investigational sites in a broad range of therapeutic areas TFS’ dedicated Recruitment Services Team handles every aspect of patient recruitment from placing

- Directory Listing

Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

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Support & Training of Investigators & Monitor...

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The Clinical Data Management unit efficiently manages all aspects of data handling in accordance with the protocol, the data management plan, efficient data capture, accurate data and timely completion of the clinical database.

- Directory Listing

Pharma Service: Clinical Trials

Category: Patient / Investigator Recruitment

Sub Category: Patient Recruitment

Patient Recruitment, rather than being a single activity is a host of responsibilities that range from protocol development and study feasibility to site selection and various activities from first-patient-in to last-patient-in. Patient recruitment and enrollment is a variable that can jeopardize drug development timeline. Delays could be caused by: Patients and investigators who are unaware of study opportunities, Difficulty accessing patients in non-traditional regions, competing protocols limiting the number of patients available to participate in studies. For successful completion of clinical studies and clinical trials goal should be to find the right patients, at the right time, to support delivery of effective study results. Informatics tools and media-based recruitment methods to identify and reach appropriate patients and investigators. The system should be able to select broad pools of quality, prescreened patients, a proven, highly efficient enrollment process, and a proper call center. Streamlining recruiting, screening and enrolling processes to Clinical Investigator. Issues with patient recruitment and enrollment are the primary causes for missing clinical trial timelines. The costs associated with patient recruitment delays are not only high, but difficult to anticipate and control. Consistently updated regulations, newly developed media by which to attract patients and investigators, and selecting appropriate service providers for recruitment all play a role in patient recruitment dynamics. There are two primary ways clinical trial managers can find patients to fill their trials: A patient can be pulled into clinical trials by way of their physician who happens to be a principal investigator for a clinical study. This method relies on the patient population of the physician/ site and the efforts of the investigator and their staff in identifying potential patients and enrolling them in the study. These types of recruitment efforts may be aided by in-practice recruiting tools (e.g. table tents, posters) and by paper or EMR chart reviews or be pushed towards clinical trials. Using this method, patients are encouraged to find a particular investigator or site, typically one they may have little or no previous contact with. Pushing patients towards clinical trials may be done through media outlets such as television, social media, billboards, radio advertisements, email targeting, etc. In addition, outside services like patient networks and patient recruitment companies identify patients and attempt to push them towards clinical trials. Primary and secondary research is conducted to uncover some of the fundamental trends in patient recruitment within the clinical trial space. Additionally, through primary research efforts, data is gathered that provide a high-level understanding of the patient recruitment outsourcing market – including both the current state of that market and future projections. Overall, the use of standalone patient recruitment service companies and patient networks is relatively low, but their penetration is expected to increase. One thing that long-time watchers of the pharmaceutical industry will know is that sponsor companies often have a hard time changing. The industry is highly regulated and processes have been built around these regulations. Taking different approaches takes time to implement. Achieving last-patient-in milestones requires extensive planning and hard data, supported by utilizing a big data engine combined with the voice of the patient, the voice of investigator intelligent and real-life scenario planning and real-life study simulations to identify, quantify and visualize the best possible development strategy. Because there are always obstacles and detours on the road to trial fulfillment, a proactive, contingency-based escalation process is to be built with pre-defined trigger points. One should possess comprehensive abilities to forecast, monitor, and manage patient recruitment, along with providing complete range of patient outreach and site-support services such as information, training, and other forms of assistance designed to minimize delays that can add millions of dollars to the cost of clinical trials. Clinical trial recruitment has to be more precise, predictable, and efficient which can be achieved by using real-world data and analytics to develop more precise study plans and select sites based on target patient population density. These new data-driven tools maximize site recruitment and activate alternative recruitment channels resulting in trial recruitment to be more efficient and predictable. Predicting enrollment more accurately, using a next generation of clinical development approach to develop site-level recruitment plans based on target population density. Increase the number of patients per site and improve patient retention rates with protocol-specific strategies for patient engagement and specialized recruitment resources, such as Clinical Trial Educators. Where needed, leverage precise online targeting to locate interested patients with cost-effective outreach strategies. Avoid delays through fully integrated data-driven recruitment tools and proactive site support. Clinical trial management service provider to the pharmaceutical, biotechnology and medical device industries and to Academia/Government constantly requires clinical trial investigators who enjoy remaining close to medical science and to the development of new medicines. Clinical trial investigators play a crucial role in the development of new medicines and with the ever expanding number of clinical trials and non-interventional research studies being conducted. Clinical studies or clinical trial patient recruitment should involve Patient-Centered Sciences, emphasising patient engagement enrolling participants for your study with a large Active Recruiting Database.

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