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  • ENGLISH
  • FRANCAIS
  • Services
    • Services Overview
    • Clinical Trial Operations
      • Protocol Development and Study Design
      • Feasibility and Study Start Up
      • Patient Recruitment
      • Project Management
      • Clinical Operations
      • Centralized Monitoring
      • Decentralized Clinical Trials (DCT)
      • Centralized eTMF
      • Medical Services
    • Regulatory and Drug Development Consulting
      • Clinical Strategy
      • Nonclinical
      • Chemistry, Manufacturing, and Controls (CMC)
      • Regulatory Affairs
      • GxP Strategy Consulting
      • Publishing and Submissions
      • Medical Writing
    • Government and Public Health Services
    • Biometrics
      • Biostatistics and Statistical Programming
      • Data Management
    • Clinical Pharmacology Modeling Simulation
      • Clinical Pharmacology Integrated Drug Development
      • Model Informed Dose & Drug Development (MIDD)
      • Pharmacometrics (PMx), Pharmacokinetics, Pharmacodynamics (PK/PD)
      • DMPK and Translational Discovery and Development
  • Therapeutic Expertise
    • Therapeutic Expertise Overview
    • By Subject
      • Oncology and Hematology
      • Rare Diseases and Orphan Drugs
      • Infectious Disease and Vaccine
      • Cell and Gene Therapy
      • Central Nervous System
      • Autoimmune and Inflammation
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  1. Home
  2. Services
  3. Clinical Trial Operations
  4. Patient Recruitment
    • Protocol Development and Study Design
    • Feasibility and Study Start Up
    • Patient Recruitment
    • Project Management
    • Clinical Operations
    • Centralized Monitoring
    • Decentralized Clinical Trials (DCT)
    • Centralized eTMF
    • Medical Services

Patient Recruitment

  • Clinical Trial Operations
  • Protocol Development and Study Design
  • Feasibility and Study Start Up
  • Patient Recruitment
  • Project Management
  • Clinical Operations
  • Centralized Monitoring
  • Decentralized Clinical Trials (DCT)
  • Centralized eTMF
  • Medical Services
    • Medical Monitoring
    • Pharmacovigilance and Patient Safety
    • Therapeutic Oversight

Understanding the patient journey is paramount for recruiting and engaging study participants. At Allucent, we have specialized expertise in this area, gained over many years working across a range of therapeutic areas and clinical study types, including on-site, decentralized, and hybrid trials. Throughout the duration of your trial, you will work directly with a patient recruitment specialist on our team, who will serve as your single point of contact and liaison with other experts at Allucent.

Our approach involves developing a comprehensive recruitment plan tailored for your study that is patient centric, data driven, and site specific. This plan encompasses enrollment projections, description of the strategies and timing of implementation, and actions to mitigate risks. Our intent is to ensure enrollment certainty and achieve on-time delivery. Key to planning your trial is developing a patient profile that identifies the characteristics of the target population while anticipating the potential burdens in order to make participation as attractive and obstacle-free as possible. This is especially critical in rare disease, where trials often involve children and families who might not live within easy travel range of the site. In these cases, Allucent offers concierge services to support patients and families as needed.

Allucent offers tailored strategies to support recruitment, engagement, and compliance, depending on the specific parameters of your initiative. For example, regarding recruitment, we are able to devise an outreach strategy that might entail use of registries, partnerships with patient advocacy groups and key opinion leaders, and on-site communications. We aim to meet your objectives while choosing tactics most appropriate for your study, timeline, and budget. We empower sites through training and education to enroll patients in your study as quickly as possible.

Your program is customized according to country regulations and sites capabilities. Using in-house resources, Allucent manages production of patient-facing materials, including translation and IRB/EC approval as necessary.

Contact Us

Let us partner with your team on bringing new therapies to light. Get in touch to get started.

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North American Headquarters
2000 Centregreen Way
Suite 300
Cary, North Carolina 27513
+1 919-361-2286

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1st Floor, One Station Square,
Bracknell, Berkshire
RG12 1QB United Kingdom
T: +44 (0) 1344 891121
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Stationsplein Noord-Oost 438
1117 CL Schiphol
The Netherlands
+31 20-4350-580