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Explore the most in-demand roles and their earning potential in 2025
Manage day-to-day trial operations at research sites. Coordinate patient visits, maintain records, and ensure protocol compliance.
Monitor clinical trials across multiple sites. Ensure data quality, regulatory compliance, and patient safety through site visits.
Monitor drug safety post-market. Analyze adverse events, compile safety reports, and ensure regulatory compliance.
Our calculator uses 2025 industry salary data from sources including PayScale, industry workforce reports, and feedback from our 30,000+ alumni network. While individual results vary based on location, company size, and negotiation, our projections reflect realistic earning potential for certified professionals.
Most students complete their certification in 4-12 weeks, depending on the program and their schedule. All courses are 100% online and self-paced, so you can study around your current job. Fast-track students often finish in as little as 2-4 weeks.
Yes. CCRPS programs are triple-accredited (CPD, ACCRE, NHA partnership) and ACE credit-recommended. Our alumni work at 1,600+ organizations including Pfizer, Moderna, FDA, IQVIA, Merck, and leading academic medical centers. Employers consistently hire CCRPS-certified candidates.
Many of our students start with zero clinical research experience. The CRC and Research Assistant certifications are designed for career changers and new graduates. We recommend starting with GCP (Good Clinical Practice) as a foundation, then adding a role-specific certification.
Yes. We offer a 14-day money-back guarantee on all programs. If you're not satisfied for any reason, contact us within 14 days for a full refund. We also offer flexible payment plans and can help you request employer tuition reimbursement.
Join 30,000+ professionals who've accelerated their careers with CCRPS certifications. Flexible payment plans available.
Explore All Programs14-day money-back guarantee · Employer reimbursement available
