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Patient Recruitment & Retention Services
👥 Maximize Enrollment and Keep Patients Engaged
CR-Link supports research sites by actively working through existing patient database, contacting eligible subjects, and managing responses from both local ad referrals and central recruitment campaigns. We ensure timely and consistent follow-up to prevent loss of interest and missed opportunities.
✅ Database review & outreach to pre-screen potential participants
✅ Call support to engage and schedule eligible subjects
✅ Management of referral flow from ads and central campaigns
✅ Retention support & strategy planning (reminders, transportation coordination, patient education)
✅ IRB-compliant materials for ethical recruitment
📩 Let CR-Link help you fill your study—fast, efficiently, and with high retention.on your budget and timeline!
Virtual Clinical Research Coordinator (CRC) Support
💻 On-Demand Study Coordination for Your Trials
Many sites struggle with staffing, leading to delays in study operations. Our Virtual CRC services offer cost-effective, remote support to help you manage essential trial tasks.
✅ Regulatory document preparation & maintenance
✅ Data entry & query resolution in EDC systems
✅ Patient follow-ups & scheduling to ensure protocol compliance
✅ Protocol training & coordination support for study teams
📩 Need extra hands for your trial? We offer short-term or long-term support with no hidden fees!
Regulatory & Document Management Services
📑 Stay Compliant & Audit-Ready
Maintaining compliance is critical in clinical research, but managing documents can be overwhelming. We help research sites organize and maintain essential regulatory documents to ensure GCP compliance and audit readiness.
✅ IRB & FDA submission assistance (protocols, amendments, informed consent)
✅ Trial Master File (TMF) & Investigator Site File (ISF) management
✅ Regulatory compliance checks to prevent audit findings
✅ Ongoing document maintenance to keep your study running smoothly
📩 We make compliance easy—work with us on your terms, no unnecessary contracts!
Remote Site Monitoring & Quality Assurance Support
🔍 Ensure Data Integrity & Compliance from Anywhere
Sponsors and CROs need reliable site monitoring to ensure protocol adherence and patient safety. Our remote monitoring services provide cost-effective oversight, reducing risks and improving data quality.
✅ Source document verification to ensure data accuracy
✅ Protocol compliance reviews to minimize deviations
✅ Audit preparation & regulatory compliance support
✅ Risk-based monitoring strategies for efficient site management
📩 Reliable monitoring support, customized to fit your budget and study needs!
Career Development Planning
🎯 Launch or Grow Your Career in Clinical Research
Whether you're just starting out or looking to advance, we help you navigate your career in clinical research with a clear, actionable plan.
✅ Personalized career roadmap based on your background and goals
✅ Resume & LinkedIn optimization for clinical roles (CRC, CTA, CRA)
✅ Interview prep and mock sessions to boost your confidence
✅ Training & certification guidance to meet industry standards
✅ Job search & networking support to connect with the right opportunities
📩 Start your career in clinical research on your terms, with expert guidance.