NCRCA’s 1‑Day Group Training for Clinical Research Professionals
🏫 Group & Onsite Training
Empower your staff with interactive, sponsor-aligned training delivered in-person or on-site. NCRCA’s Group and Onsite Training is specifically designed to streamline certification for employer-partnered organizations—giving teams the tools to succeed in regulated clinical trials.
🚀 Why Group Training Works
- Excel with Hands-On Learning
Sessions include both the written assessment and practical proficiency, especially critical for technical roles like phlebotomy and patient care. - Consistent Standard, One Session
Staff learn standardized exam content and clinical research protocols together—ensuring team-wide understanding and compliance. - Employer-Managed Implementation
Accredited organizations plan the sessions and schedule staff, while NCRCA provides testing materials and proctors. - Cost-Efficient & Time-Saving
Group pricing, fewer scheduling conflicts, and efficient exam delivery maximize productivity and minimize downtime.
👩‍⚕️ Credential Training Offered for Employers:
| Credential Code | Credential Title | Training Focus |
|---|---|---|
| NCCRPT | Clinical Research Phlebotomy Technician | Adult phlebotomy, specimen accuracy, FDA/GCP compliance |
| NCCR‑PPT | Clinical Research Pediatric Phlebotomy Technician | Pediatric phlebotomy, consent of minors, comfort techniques |
| NCCRMA | Clinical Research Medical Assistant | Intake assessments, vital signs, protocol adherence |
| NCCRPCT | Clinical Research Patient Care Technician | Patient monitoring, transport, safety procedures |
| NCCRAA | Clinical Research Administrative Assistant | Documentation procedures, data entry, scheduling support |
| NCCRT | Clinical Research Technician | Lab prep, device operation, EKG & imaging support |
| NCCRAS | Clinical Research Assistant Supervisor | Staff supervision, QA checks, clinical task coordination |
| NCCRD | Clinical Research Director | Operational leadership, protocol oversight, sponsor liaison |
| NCCRTM | Clinical Research Trials Manager | Study logistics, data workflow, cross-site management |
| NCCRP | Clinical Research Professional | Advanced protocol support including ethics, data, and compliance |
| NCCRA | Clinical Research Assistant | Entry-level research support, consent documentation, intake logs |
🧾 Session Details & Structure
Who Participates: Employers bring staff who require certification—whether front-line, admin, or leadership roles.
Session Format:
- Written examination covering role-specific content and regulatory compliance
- Practical testing for direct patient-care credentials (e.g., phlebotomy)
Learning Tools Provided:
- Official NCRCA training manuals
- Role-based study guides (e.g. pediatric-specific protocols)
- Exam proctors trained in NCRCA standards
Certification Completion Path:
- Staff must pass the written exam and practical skills assessment
- Certifications and CEU eligibility are confirmed within 48–72 hours
âś… Benefits of Working with NCRCA
- Standardizes knowledge and performance across all staff
- Supports sponsor and regulatory audit readiness
- Minimizes credentialing delays with centralized setup and execution
- Supports repeat sessions for new cohorts or roles
đź“ž How to Schedule Your Group Training
- Eligible employers begin by submitting a Letter of Intent to join NCRCA’s employer partnership program.
- Once approved, coordinate your training needs with our team to plan dates and credential tracks.
- NCRCA provides proctors, venue documentation, and exam materials.
- Exams are administered, scored, and certifications issued within days.
- Maintain compliance with ongoing CEU credits and employment-hours reporting.
🧩 Use Cases
- Hospital training days for front office and clinical support staff
- Multi-site pharma partner rollouts to standardize credentialing across facilities
- Academic or vocational school integration for hands-on student credentialing