C.E.O Timkings International Associates Limited. Location: Nigeria West Africa. Phone: +2348160404563. Email: timothyekwebelem@timkintelclconsult.com
The CEO Timothy Ekwebelem, the owner of Timkings International Associates Limited has contributed immensely in the Development of Pharmaceutical and Clinical Research with a strong focus and vision of placing fresh and in-experienced graduates globally into industry of Pharmaceutical and Clinical Research without necessarily having the required experience in the industry and also those from other careers who might like to convert from their present careers into clinical research were given the opportunity to be trained and automatically be given a permanent employment at the Timkings International Associates Limited. TImothy Ekwebelem, a graduate of Queen Mary University of London, University of Greenwich London, Kingston University London and James Lind Institute has worked with top British Professors in Clinical Pharmacology , Hematology and Microvascular and with a sound Distinctive Education and very solid family background , Timothy grew up to learn the importance of team work and with his excellent background and experience in the field of Clinical Research he Co-Authored and Published many Research Findings with Top British and American Professors like Professor Athol Johnston of William Harvey Research Institute London, Professor Arthur Tucker of Saint Bartholomew's Hospital London, Professor M. Heat and Professor Telfer of the Royal London Hospital in different Academic Peer Review Journals like E-online Journal of British Pharmacology Society, Willaim Harvey Research London etc. Timothy Ekwebelem also independently Published the Outcome results of his novel studies in different medical Peer Review Journals and has worked in different Therapeutic areas. Having acquired enormous experience and knowledge in different studies, Timothy Ekwebelem built a vision which championed so many trainees into training from being student trainees on his online clinical research training program to successfully becoming full time staff of the Timkings International Associates Limited immediately after completing their compulsory intensive training. Trainees from clinical and non- clinical background are giving an automatic employment/ work placement at the Timkings International Associates Limited after the successful completion of their program where he heads as the CEO and the founder of the company. He also partners with other Organizations in placing trainees on immediate employment. Timothy Ekwebelem with expert Knowledge and years of experience in the industry of Clinical Research, knows exactly what to do to carve trainees students into top-class clinical research professionals. Timothy Ekwebelem is a world class CEO and a consultant Clinical Research Professional, and he is all about delivering the best services to the world of Clinical Research/ global work Force, a task he is bent on achieving , blended with his vision of planting offices in Major Cities of the world , striving to reducing global Un-Employment by making a global impact in the delivery clinical /medical research. Timothy believes people should be given the opportunity to work which he is doing presently with good intent, dedication and commitment to fulfilling his visions. TImothy Ekwebelem grew up in Willesden Green, the Northwest of London United Kingdom and loves Research and Development with great passion to discovery science and he has very strong belief, trust, faith and fear in the Lord God Almighty. Welcome to Timkings International Associates Limited where dreams come alive.
Medical Science Liaison / Clinical Trial Manager. Location: Atlanta Georgia USA.Phone: +1 (407) 668-7975.Email Address: veroniqueintel@timkintelclconsult.com
Dr. Veronique Pryce Carney is a Medical Science Liaison with Timkings International Associates Limited, where she supports scientific engagement and medical strategy across Immunology, Dermatology, and Rare Disease therapeutic areas. Dr. Veronique is a product of the Timkings International Associates Limited Professional Clinical Research Training Program, an excellent Medical Personnel , and once a trainee of the Timkings International Associates Professional Clinical Research Associates Training Institute and currently she has successfully transitioned automatically as the Timkings International Associates Limited Medical Science Laison/ Clinical Trail Manager that covers Atlanta Georgia and other nearby Region. Dr. Veronique is dedicated to translating complex scientific concepts into clear, practical insights that enhance evidence-based care. In her role, Dr. Pryce works closely with healthcare providers, key opinion leaders, and clinical researchers to share new scientific data and support real-world medical needs. She builds strong partnerships, supports investigator-initiated studies, and helps communicate important developments in the field. Guided by curiosity and a passion for patient-focused science, Veronique aims to connect new scientific advances with everyday clinical practice through open and meaningful collaboration
Senior Start-Up Regulatory Specialist. Location: OHIO USA . Phone: +1 (210) 244-3593. Email Address: timekwebs101@timkintelclconsult.com
Maisha Dramiga is a Senior Start-Up Regulatory Specialist Staff ofTimkings International Associates Limited based in OHIO United State of America. Maisha first completed our Professional Clinical Research Training Program successfully with top distinctive classification and automatically became employed at the Timkings International Associates Limited as a Senior Start-Up Regulatory Specialist. Being an American and expert in the field of clinical research and having followed the company's training curriculum successfully, she became in charge of all Regulatory applications and submissions and the overall supervision of her assigned Regulatory Start-Up Specialist in our organization. Maisha is originally from San Antonio, Texas, and a proud American graduate from Baylor University and an alumnus of the same University. She’s worked across clinical operations, study start-up, and regulatory workflows, keeping research projects organized, and strictly adhering to the guidelines of regulatory standards required by the regulatory body, and moving things forward in company's assigned project studies. Maisha loves collaborating with teams, simplifying complex processes, and making sure every detail lands exactly where it should be. With experience ranging from IRB submissions to quality oversight, she brings reliability, curiosity, and a little bit of sparkle to every project she touches. When she’s not deep in study documents, you’ll find her exploring new cities, enjoying nature, or discovering her next favorite hobby.
Clinical Trial Manager
Dissirama Reine Betimbena is the Clinical Trial Manager at Timkings International Associates Limited covering major sites at the city of Cincinnati and all parts of OHIO in the United States. Reporting directly to the CEO, Miss Dissirama enrolled and went through our Professional Clinical Research Training on a six weeks intensive , rigorous and comprehensive training and was automatically employed as a Clinical Trial Manager for Timkings International Associates Limited on the successful completion of the compulsory training. Miss Reine holds a bachelor's degree in health sciences from Trident University International United States, and at the same time also currently pursuing a Master of Science Degree in Clinical Research at Boston University also in United State of America. Miss Dissirama Reine is a hardworking , focused and dedicated individual who has put so much effort in making sure all studies were conducted according to Good Clinical Practice and that patients safety , interest and welfare were protected and that studies were strictly conducted according to the protocol of the study and that the CRAs working under her were working according to regulatory and ethical standard guiding clinical research and that all studies are verified, entered and reported correctly according to GCP (Good Clinical Practice). Dissirama Reine is one of the living testifiers that our professional training program can genuinely benefit our trainees after training, and she occupies a managerial position at Timkings International Associates Limited and also hopes to climb into a more senior position in the future. Miss Reine services at our company can be termed as excellent garnished with Brillant innovative and detailed approach to work.
Clinical Research Operations Manager
Miss Goodness Udochukwu Anwuchughum is the Clinical Research Operations Manager at the Timkings International Associates Limited. Miss Goodness first enrolled as a student trainee on the Timkings International Associates Limited Professional Clinical Research Program. She successfully completed the Clinical Research Professional Training Program with a Distinction Classification and was automatically employed at the Timkings International Associates Limited as the company's Clinical Research Operations Manager covering Africa, Europe, Asia and America. Miss Goodness Anwuchughum is a product of the Professional Clinical Research Program of the Timkings International Associates Limited program and now holds an important position in our organization. She is a graduate of University of Greenwich London and holds the Degree of Bachelor of Science Business Information Technology with Second Class Honours First Division. She also holds an International Advanced Diploma in Computing at the Informatics Academy Singapore, and International Diploma in Computing at the Informatics Academy Singapore. Miss Goodness Anwuchughum is a hardworking, dedicated, focused staff that helped in the Optimum successful level outcome of the company's vision, culture and success. Having finished with High Class Distinction in our company's Professional Clinical Research Training program , she did not find it difficult in settling down with the new position she occupies at the Timkings International Associates Limited. A role model for the junior workers , her modest and detailed approach to work and her combination of business acumen and excellent computing technology skills makes her an outstanding worker in our organization.
Clincal Trial Manager
Adela Lum Asanga is currently a Clinical Trial Manager at the Timkings International Asociates Limited after successfully completing the Timkings International Associates Limited Professional Clinical Research Training a graduate of distinctive class , she has successfully completed different assigned studies of the company. She covers the whole of Kigali and has proven that she can deliver projects on assigned tight deadlines and the future holds for her a career growth in thr organization of Timkings International Associates Limited. She is a focused minded individual with the zeal to succeed all the times and has the ability to take any challenging role in the company.
Clinical Trial Manager
Ande Praveen Kumar is a Clinical Trial Manager at Timkings International Associates Limited, where he supports and oversees clinical studies across the United Kingdom and the United States. Praveen joined Timkings International Associates as a Trainee under the Timkings Professional Clinical Research Programme. He successfully completed the Clinical Research Professional Training Program with a Distinction classification, following which he was automatically employed as a Clinical Trial Manager at the organisation. The programme was well structured and delivered a detailed curriculum that provided strong theoretical foundations alongside extensive hands-on practical simulation experience, preparing him effectively for real-world challenges within clinical research organisations. He holds a Master’s degree in Pharmacy from Annamalai University, India, and has approximately 15 years of professional experience in Pharmacovigilance (Drug Safety). His extensive background in drug safety has enabled him to bring a strong patient-focused and compliance-driven approach to clinical trial management. In his current role, Praveen builds strong partnerships with investigators, supports investigator-initiated studies, and contributes to the effective communication of important scientific and operational developments. His work directly supports the development of new products and interventions, with a consistent emphasis on patient safety and regulatory compliance. All clinical studies under his management are conducted in strict accordance with Good Clinical Practice (GCP) guidelines and adhere closely to approved study protocols. Praveen has consistently demonstrated the ability to manage and complete sponsor-assigned studies within agreed timelines, contributing positively to both study delivery and the overall growth and reputation of the organisation. His strong organisational skills, regulatory knowledge, and commitment to high-quality clinical research continue to support the advancement of safe and effective medicines for patients.
