CLINICAL RESEARCH PROFESSIONAL PROGRAM
Start your career as a Clinical Research Coordinator (CRC), Clinical Research Associate (CRA) or in many other integral roles in this exciting field
ABOUT US
The Accredited Clinical Research Postgraduate Certification program CRP 3.0 covers Canadian, US, and International GCP regulations for clinical trial conduct. It is designed to support professionals in career change until they are hired, by preparing them with theory, practice and personalized 1:1 support including interview preparation, CV advice and more. Our ONLINE program is individual, self-paced, with unlimited 7/7 LIVE support adapted to the goals of every student. Individual, self-paced, ONLINE program with unlimited 7/7 LIVE support, adapted to the goals of every student.
WHY US?
+1000 PAGES GCP TRAINING
DRUG & DEVICES EDC INTERNSHIP
CV & INTERVIEW PREPARATION
NETWORKING & CAREER EVENTS
JOB LEADS AND REFERRALS
OUR PROGRAMS
The course is entirely online and self-paced. Many of our students complete the course in 6-9 months, working on it part-time. Beyond the theoretical foundations of clinical research, we provide a self-paced program adapted to the goals of every student.
- LIVE support directly by tutors, 7 days a week till late evening
- Monitoring internship in 2 old real-life phase II/III studies to provide the "hands-on" experience in Canadian/US regulatory environment, required by the law.
- 28 chapters of material, to be completed at your own pace
- Personalized CV adaptation for each position that you will apply for
- Placement Assistance Till Hired (PATH) to provide personalized coaching on job-search techniques and networking, plus 1-on-1 preparation for every interview
- Interview preparation and unlimited mock interview practice using Pitch-on-Air video software
- Internship tasks including Electronic Data Capture (EDC) and practice on a Clinical Trial Management System (CTMS)
- Networking coaching and guidance with Professional Branding support
- Regular networking and career events
- Advanced notification of jobs when available (unlisted jobs and through recruiters)
COURSE OUTLINE
Our Accredited Post-Graduate Clinical Research Onboarding Program provides an international certification on the clinical trials regulatory affairs and the foundation of the GCP fundamentals and clinical trials regulations worldwide including the following non-exhaustive list of topics:
- History of clinical research regulations
- Clinical trial phases
- Clinical research roles
- The foundation of GCP guidance
- FDA and US regulations
- Canadian and international regulations
- Ethics board/IRB/IEC/REB
- Informed consent process
- Adverse event reporting and safety
- Study design general considerations
- Protocol development
- Case report forms design
- Subjects recruitment and retention
- Site evaluation and selection
- Site initiation study start-Up
- Monitoring visits
- Study close-out
- Fraud and misconduct
- Data management
- Private Information Protection
- Data safety monitoring boards
- Electronic Data Capture
- Audits and inspections
- Essential documents and archive
- Medical devices
WHO IS ELIGIBLE?
Candidates worldwide with nursing or any university degree
Research assistants, interested to join this rewarding industry
Professionals in career change (MD, DDS, DVM, BPharm, PharmD, RN)
