Our Team
Our Incredible Team
OrciTrials’ board of directors consists of veteran clinical research professionals with over 70 years of cumulative leadership experience in CROs and Pharmaceutical companies across UK, Pakistan, APAC, ANZ, and Europe.
Our team is also highly skilled and experienced in every aspect of clinical development across all therapeutic areas.
Team
The unwavering strength and unity of our team
Kafait Ahmad (VP, Clinical Operations)
Mr Ahmad brings over 15 years of clinical research experience having held a wide variety of leadership roles within Pharma Companies & CROs and has detailed experience of directing global clinical trials across phases I-IV.
He is Skilled in Team management, Project Management, Oncology, Clinical Data Management, and Clinical Monitoring with a Master’s in Clinical Research from University of South Wales.
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Hassan Iqbal (Chief Operating Officer)
Mr Iqbal is an Actuary who has worked with various Insurance firms in the UK over the last 12 years. He has extensive experience of statistical analysis, risk management and has a special interest in Clinical Research.
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Mr. Steven Bukvic (Global Head of Business Development)
Mr. Steven Bukvic graduated from Coventry University in 1982 with a degree in Applied Biology. After serving in the commercial sector of the UK motor industry for 8 years, Steven joined the Pharmaceutical Industry in 1990. For the next 33 years Steven’s career in the Pharmaceutical / CRO sectors has covered a broad range of disciplines within the field of clinical research, including clinical site monitoring, project management, pharmacovigilance, training, QA and business operations. Steven has worked in Covance, GSK, MSD and Pfizer to name just a few of the multi-national companies in his career. Steven was instrumental in establishing a CRO in Asia as well as successfully building the ACROSS Global CRO Alliance. He has also had extensive geographical exposure having worked in the UK, US, Germany, China and the Russian Federation. Steven is an active consulting partner for OrciTrials and has travelled on multiple business trips to Pakistan.
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Naeem Noordin (Non-executive Director)
Naeem Noordin, driven by an insatiable curiosity and commitment to excellence, embarked on a remarkable journey in clinical research over his 25-year career. His passion for science led him to specialize in pharmacokinetics and early Phase I clinical trials, forming a solid foundation for his future contributions. Rising swiftly to senior positions such as Head of Clinical Operations and Head of Learning and Development, Naeem demonstrated exceptional leadership and talent nurturing skills. He has collaborated with health ministries worldwide to develop and refine clinical trial regulations, enhancing global standards. Committed to continuous learning, he offers cutting-edge ICH GCP and clinical development related training and consultancy, fostering industry excellence. In 2013, he founded Siara Limited in London and later expanded to the UAE with Siara Consultancy FZ LLC, showcasing his visionary leadership and global reach. Naeem’s diverse experiences from living and working in the US, Asia, and the UK have enriched his innovative approach and understanding of global clinical research environments. His legacy is marked by his dedication to excellence, innovation, and global collaboration, inspiring researchers and professionals worldwide.
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Brian K Norton (Business Development Director)
Brian has more than 17 years of clinical trial experience. Brian founded ClinTrial Networks (CTN) in 2007 and has leveraged both his business and extensive clinical trial experience and created a network of dedicated research sites worldwide. Brian has the ability to support Phase I to Phase IV research programs covering a wide range of medical and psychiatric indications.
Brian currently serves as the Business Development Director for OrciTrials. The advantages of Brian’s trial sites are they have large clinical practices with sufficient patients to meet enrollment goals. This is a very key component for patient recruitment and retention. In addition to Brian’s role as BD Director, sponsors and CROs seek Brian out to locate quality sites saving less time and money for the sponsor. Brian’s sites are located throughout the U.S., Canada, Mexico, Puerto Rico, U.K., Spain, Russia, New Zealand and Australia.
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Azam Jafri (Regulatory Manager)
Mr. Azam Jafri is a highly seasoned professional with an extensive career spanning approximately 20 years in the healthcare industry. He has amassed a wealth of experience through his work in multiple countries across Southeast Asia, with a particular emphasis on regions such as Pakistan, Central Asia, the Far East, Africa, and Europe. His expertise encompasses critical domains, including Sales, where he has demonstrated a remarkable ability to cultivate and manage relationships with clients and stakeholders. In Marketing, his proficiency in devising and executing strategies that enhance brand visibility and market presence. Furthermore, in Business Development, consistently identifying growth opportunities & establishing strategic partnerships. His competence extends to Regulatory Affairs, where he has displayed a deep understanding of the intricate regulatory landscape, ensuring compliance and the efficient operation of healthcare initiatives.
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Olga Peycheva (Regulatory Manager UK)
Olga Peycheva is an accomplished regulatory advisor, based in UK with over 18 years of extensive experience across the UK, Ireland, Germany, and Bulgaria. Holding diplomas in Quality Management and degrees in Biophysical Chemistry and Biotechnology, she is certified in GCP, Pharmacovigilance, European Medical Devices Regulation, and Medical Writing. Olga’s expertise encompasses study start-up, monitoring, regulatory affairs, and project management, covering a diverse range of therapeutic areas including oncology, hematology, infectious diseases, respiratory diseases, cardiology, and autoimmune diseases. She has managed both medical device and drug trials, demonstrating proficiency in various systems such as eTMF, EDC, IVRS, and regulatory submission platforms. Additionally, Olga is actively engaged in volunteer work, serves on the Research Ethics Committee, and is affiliated with Regulatory Affairs Professionals Society (RAPS) and Research Ethics Association
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Ahmad Kamal (Head of Project Management)
Dr. Ahmad Kamal is a seasoned clinical research professional with a Ph.D. in Pharmaceutics, specializing in drug development and translational research. Currently serving as a Clinical Project Manager at OrciTrials, he adeptly oversees team development, coaching, and the successful execution of projects. With over 14 years of industry experience, Dr. Kamal has demonstrated prowess in establishing clinical research infrastructure and effectively managing global and local trials across Pharmaceutical and Contract Research Organization (CRO) platforms.
His journey in clinical research began as a Jr. Clinical Research Associate, steadily advancing to roles such as Senior Clinical Research Associate, Local Trainer, Back-up Regulatory Contact, and Risk Coordinator during his tenure at GlaxoSmithKline Pakistan Limited. Noteworthy achievements include spearheading Biological Studies in Pakistan, pioneering the Cold Chain Management infrastructure for vaccine trials, and achieving record recruitment rates at GSK. His leadership steered 09 projects as Project Lead and contributed to numerous clinical trials spanning Oncology, Infectious Diseases, Metabolic, and Pediatric and Adult vaccine research, encompassing both interventional and non-interventional studies, as well as RWE studies of various complexities.
Dr. Kamal’s expertise extends to quality assurance, having conducted over 10 audits globally within the CRO landscape. Additionally, he had been involved in quality management initiatives, conducting internal assessments for studies and system tools in the MENA region, vendor audits and quality checks for organization standards. Proficient in developing operational processes and quality systems, he also dedicated three years to public health programs in collaboration with government agencies. This diverse array of experiences equips him with a wealth of knowledge and expertise poised for driving project success in Pakistan at OrciTrials.
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Yvonne Li (Quality Assurance Auditor)
Ms. Li, a Quality Assurance Professional, holds extensive experience of 18 years in Clinical Research and Auditing services compliant to GCP. Her specialty lies in Risk Management, Vendor Management and Performance Management. She has worked with multiple CROs across the globe to deliver quality compliant services in Singapore, China, Indonesia, Philippines, Malaysia, and Australia.
OrciTrials together with its partner provides its clients with GCP compliant services ensuring cost effectiveness and high-quality outcomes. We provide services tailored to the needs of our clients to help them excel in the market with top-notch results. OrciTrials together with its partner is delighted to serve you.
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