WHY A CAREER IN CLINICAL RESEARCH? Medical advancement ultimately depends on medical experimentation (Declaration or Helsinki) Medical research is extremely important to improve, innovate and discover new treatments and possible cures for once incurable diseases. The players, the pharmaceutical industry and academia work very hard to meet that challenge. Ultimately, clinical research can provide to the qualified researcher real application of scientific knowledge EDUPHARMA 2012 COPYRIGHT REWARDING CAREER A career in clinical research is highly rewarding, although most of the potential therapeutic candidates never make it to the market (>85%), the knowledge acquired is extremely important to further improve human lives. Here you see science in action, and where we make the transition from BENCH to BEDSIDE EDUPHARMA 2012 COPYRIGHT A CAREER IN CLINICAL RESEARCH THE MEDICAL OR DENTAL PROFESSIONALS SCIENCE AND OTHER H E A LT H P RO F E S S I O N A L S Actively participate in the discovery on new therapies/treatments Provide valuable feedback to improve therapies Follow up on new therapies to allow keep patients safe Participate in the decision on what works and what does not Clinical research is a highly regulated activity Science professionals from different backgrounds are involved in all aspects of the research process Know how you also can, if properly qualified, be a clinical science professional EDUPHARMA 2012 COPYRIGHT A CAREER IN CLINICAL RESEARCH Science and other health professionals What makes you a qualifying candidate? You should have minimum a Bachelors degree in science or health related discipline or equivalent 4 year post secondary education Who applies for these jobs? biologist, biochemist, professional nurse, chemist, molecular biologist, statisticians, data managers, Information Technology specialist, pharmacists, pharmacologists, to name a few. EDUPHARMA 2012 COPYRIGHT HOW DO I BECAME A CLINICAL RESEARCH PROFESSIONAL Basically you have to besides qualifications, demonstrate training and knowledge in: The drug development process Regulatory requirements, local and global Good clinical practices, good laboratory practices Ethical aspects of clinical research Data management Electronic systems in data collection Project management Business management EXPERIENCE EDUPHARMA 2012 COPYRIGHT KEY ASPECTS Select the right training program Acquire relevant experience Marketing skills Good dominion of the language EDUPHARMA 2012 COPYRIGHT HOW CAN WE HELP YOU ACHIEVE YOUR GOALS OTHER PROGRAMS • There are numerous courses, seminars, web based training for clinical research out there. • Most of them are limited to theoretical knowledge based on published regulations and guidelines • They target a limited audience • Those programs are very expensive and sometimes taught only in some countries, making it inaccessible to potential students from South America, Eastern Europe, India and China due to either visa restrictions or web connectivity limitations. EDUPHARMA 2012 COPYRIGHT HOW CAN WE HELP YOU ACHIEVE YOUR GOALS EDUPHARMA • We are completely different, our approach is face to face training where you can talk and meet the instructors and further enhance the training with personal experience in the industry • Our programs are based on actual CASE studies and application of the requirements and regulations with extensive practice • We have extensive knowledge of the industry and are aware of what it needs • We provide basic, and advanced training according to your experience • Our programs are financially accessible to most potential candidates • Upon completion of the necessary modules at your own peace you can achieve Certification by our institution and maintain it in a very simple way • At EduPharma you do not need to have clinical research experience to start training for clinical research • We are located globally EDUPHARMA 2012 COPYRIGHT WHICH ARE OUR TRAINING PROGRAMS 1. Introduction to clinical research (2 full days) 7. Consenting the subject volunteer, a process (2 full days) 2. Good Clinical Practices ( 2 full days) 8. 3. Clinical Research for the Principal investigator (2 full days) Risk based approach to monitoring clinical trials (2 full days) 9. 4. Clinical Research for the Coordinator (2 full days) Master Certificate in Pharmaceutical R&D and Business Management (6 full days) 5. Clinical Trials Data management and resolution (2 full days) 10. Good Clinical/Laboratory Practices in Clinical Research (2 full days) 6. Introduction to Electronic systems in clinical research (1 full day) 11. Cost Estimates and Resource Allocation in Clinical Trials (2 full days) 7. Biotechnology in clinical research (2 full days) 12. 8. Pharmacogenomics in drug development (1 full day) Training Program for Institutional/Ethics Review Board Members (1.5 days) More programs will be added as they are developed to meet professional needs All courses are presented in ENGLISH EDUPHARMA 2012 COPYRIGHT THE ADVANTAGE OF TRAINING WITH EDUPHARMA EXCELLENCE: We offer excellent programs designed to meet industry needs. ACCESSIBILITY: Our tuition fees are accessible for the individual trainee and the industry. ACADEMIC QUALITY: Our instructors are highly qualified clinical research professionals All materials are provided Locations are accessible to participants all over the world All programs and materials are in English Dual certificate issued by The Clinical Research Institute of America and EduPharma EDUPHARMA 2012 COPYRIGHT OUR GOAL To provide each and every trainee to the tools necessary to ENTER, ADVANCE and EXCEL in pharmaceutical clinical research and development Contact Us now, and we will tailor the programs that are best for you EDUPHARMA 2012 COPYRIGHT