About Us
Our Story
Founded in 2025, SciecneLiv was established with the vision of bridging the gap between academic knowledge and real-world expertise across healthcare, clinical research, and life sciences sectors. Our founders, seasoned professionals in these industries, recognized a growing need for accessible, high-quality training programs that equip individuals with the specialized skills essential for success in today’s competitive job market. Since our inception, we have been dedicated to delivering industry-driven courses designed by experts with real-world experience.
We collaborate with renowned educators, industry specialists, and thought leaders to offer comprehensive, career-oriented learning. Our online platform provides professionals from around the globe with flexible, practical training in clinical data management, medical devices, life sciences innovations, and other key areas within these rapidly evolving sectors.
At ScienceLiv, we specialize in providing high-quality, industry-relevant training in clinical research, regulatory compliance, and data management. With a team of expert instructors holding advanced degrees and years of professional experience, our mission is to empower professionals with the skills and knowledge needed to excel in their careers.
What sets us apart is our focus on real-world applications and regulatory standards, ensuring that our courses are not only educational but also aligned with the latest industry trends and regulations. We are committed to providing accessible, career-oriented learning that helps individuals advance in the ever-evolving healthcare and life sciences innovation.
Mission & Vision
Mission
At SciecneLiv, our mission is to empower professionals in the healthcare, clinical research, life sciences, and other related industries by providing accessible, high-quality, and career-oriented education. We aim to deliver industry-relevant courses led by experts, ensuring learners gain the knowledge and skills to excel in their careers and contribute to the advancement of global standards in clinical research, regulatory compliance, and life sciences innovation.
Vission
Our vision is to become a global leader in providing transformative education that bridges the gap between academic learning and industry expertise. We aim to equip individuals with the skills needed to meet evolving regulatory standards, drive innovation, and advance careers in healthcare, clinical research, and life sciences. In addition to our comprehensive courses, we offer workshops, webinars, consultancy services, and Quality Management System (QMS) support to further enhance learning and practical application. Through continuous learning and professional development, we strive to foster a more skilled, compliant, and forward-thinking workforce that shapes the future of healthcare and life sciences education.
5+
3 K
WHY CHOOSE SCIENCELIV
The Best Beneficial Side
of ScienceLiv
Industry-Relevant Curriculum
Gain practical knowledge and skills aligned with current clinical research and pharmaceutical industry standards.
Unlimited Lifetime Access
Access course materials anytime, anywhere — revisit content and resources as often as needed, with no expiration.
Learn from Experienced Professionals
Be guided by seasoned clinical data managers and research experts with real-world industry insights.
TESTIMONIALS
What Our Learners
Say About the Course
Hear from professionals and aspiring clinical data experts who have transformed their careers through our comprehensive Clinical Data Management course. From mastering EDC systems and query handling to understanding regulatory standards and audit readiness, our students gain industry-ready skills that open doors to opportunities in clinical trials, CROs, and pharmaceutical R&D.
Great Support Team
Very Powerful
Excellent Service
Course Instructors
Dr. Emily Carter
Clinical Data Management Lead with a decade of expertise in EDC systems, and GCP-compliant data practices.
Mr. Lucas Bennett
Regulatory Affairs Consultant specializing in international standards, FDA/EMA submissions, and risk assessment.
Dr. Jonathan Miller
Senior Clinical Research Scientist with 15+ years of experience in global clinical trial management and protocol design.