Foundational
ICH-GCP E6(R3) Certification
The updated Good Clinical Practice standard — principles, investigator responsibilities, essential documents and audit-readiness.
24 hrsBeginner → Intermediate
New cohort starting March 2026 — limited seats
Your gateway toglobal clinical research.
Industry-designed training in GCP, monitoring, data management, safety and regulatory affairs — taught by working CRAs, medical monitors and QA leads from top CROs.
- 12,400+
- Learners trained
- 38
- Countries reached
- 94%
- Placement in 6 months
- 4.9/5
- Learner rating
Accredited by TransCelerate BioPharma
Certificates recognized across 38 countries
Our graduates work at
IQVIAParexelSyneosICON plcNovartisFortrea
Curriculum
Courses that build a real clinical research career.
Six career-mapped programs, each combining live instruction, SOP walkthroughs and hands-on simulations in production-grade tools.
Career track
Clinical Research Associate (CRA)
End-to-end monitoring workflow: site selection, initiation, routine monitoring visits, close-out and remote source data verification.
60 hrsIntermediate
Career track
Clinical Research Coordinator (CRC)
Site-side execution: consent, protocol adherence, IRB submissions, subject recruitment and query management.
48 hrsBeginner → Intermediate
Specialization
Pharmacovigilance & Drug Safety
ICSR processing, MedDRA coding, PSUR/PBRER authoring and signal detection in a modern safety database.
40 hrsIntermediate
Specialization
Clinical Data Management
CDISC SDTM, EDC build in Medidata Rave & Veeva, query lifecycle, database lock and CDASH standards.
36 hrsIntermediate → Advanced
Advanced
Regulatory Affairs — Global
FDA, EMA, CDSCO and PMDA submissions. IND / CTA / NDA lifecycle, eCTD structure and agency correspondence.
50 hrsAdvanced
Learning pathway
From enrollment to your first CRA role.
- 01
Enroll & onboard
Diagnostic call, learning plan mapped to your background and target role.
- 02
Live cohort + labs
Weekly instructor-led sessions with EDC, eTMF and safety database simulations.
- 03
Capstone project
Run a mock study — from protocol synopsis to database lock, reviewed by senior CRAs.
- 04
Certify & place
Sit the certification, get a verified digital credential and interview with our hiring partners.
Faculty
Taught by practitioners, not lecturers.
Every instructor is currently working in a CRO, sponsor or regulatory body. You learn the SOPs and tools being used on trials this quarter — not textbooks from 2015.
42 industry instructors · avg. 14 years experience
Dr. Aditi Rao
Senior Medical Monitor · Ex-Novartis
Oncology & rare disease
Marco Alves
Lead CRA · Ex-IQVIA
Risk-based monitoring
Priya Menon
Head of PV · Global sponsor
Signal detection, PSUR
James Okafor
Regulatory Affairs Director
FDA & EMA submissions
Outcomes
Certification that opens doors — globally.
Our credential is verifiable on-chain and recognized by leading CROs and sponsors. 94% of full-track learners secure a clinical research role within six months of certification.
- Verified digital badge & printable certificate
- Interview prep + 1:1 CV review with hiring partners
- Access to a private alumni network of 12,000+
- Lifetime access to course updates as regulations evolve
SCG Verified Certificate
ID · SCG-2026-04-{cohort}
“The GCP + CRA track got me hired at Parexel three weeks after certification. The mock monitoring visits were the closest thing to the real job I'd seen anywhere.”
— Sara Ibrahim, CRA I · Parexel
Apply
Start your clinical research career.
Tell us where you are and where you want to be — we'll map a program and reply within one working day.
📞 +1 (415) 555-0148
✉ admissions@sciphera.global
🌐 Live cohorts in EN · ES · HI · AR