Team
Timothy Ekwebelem PhD. Location: Califonia, USA. Phone: +1(209)9731016.
C.E.O, Program Director TimKings International Associates Limited.
Timothy Ekwebelem is the owner, founder and the CEO of Timkings International Associates Limited, a global Contract Research Organization, Pharma industry, Clinical Research Consultancy and Clinical trial training Institute. As the CEO, Timothy holds the degree of PhD in Clinical Drug Development of Queen Mary University of London, Master of Science Degree Clinical Drug Development Queen Mary University London, Advanced Postgraduate Diploma Clinical Research and Medical Writing James Lind Institute India, Master of Science Pharmaceutical Analysis Kingston University London, Bachelor of Science Degree Hons Pharmaceutical Sciences University of Greenwich London. As the CEO he is the chairman and the head of board of directors of Timkings Associates Company's Ltd with headquarters is in Alameda California, United States and branches in London, United Kingdom, Owerri, Nigeria, Kigali, Rwanda, Germany, Amsterdam, Netherlands and Ontario, Canada. Our Organization is an expert Contract Research Organization with years of experience in clinical trial research, combining our expertism in regulatory application/submission, start-up , maintenance and closeout, we help sponsors ease their clinical trials seamlessly, helping to solve the problem of regulatory hurdles to the actual completion of clinical trials, strictly adhering to regulatory compliance, GCP principles, bearing in mind importance of patients safety and maintaining ethics in clinical research. We are expert in contract and budget, Clinical Data Management and EDC Build Services, Quality Management Systems (QMS) and Audit, Regulatory Affairs, Ethics and Compliance Specialist, Clinical Data Technology Enablement, Quality Management and GxP Compliance (SOP, Audit, Capa), Study Start-Up and Site Activation, Oncology, Cardiovascular, Hypertension, Diabetes, Hematology, Microvascular, Dermatology, Ulcerative, HIV, Respiratory, Rare Diseases, Sickle cell etc. Our staff are all expert trained professionals with more than 5 years of experience and all GCP certified. Timothy Ekwebelem has worked with top British Professors in Clinical Pharmacology, Hematology and Microvascular and with a sound Solid Distinctive Education and strong family connections in the industry. Timothy Ekwebelem with excellent background and experience in the field of Clinical Research was able to co-author and published many research studies 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 Institute London, British Medical Journal, American Journal of Molecular Biology etc. Timothy Ekwebelem is the overseer of the Timkings umbrella of companies while His God the Almighty Jehovah is the Owner of original owner of Timkings International Associates Limited. Welcome to Timkings International Associates Limited where dreams are coming alive and trainees turning into Professional CRAs, CTMs etc.
Miss Goodness Udochukwu Anwuchughum. Location: London UK.
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.
Dr. Veronique Pryce Carney. Location: Atlanta, USA. Phone: +1(407)6687975
Medical Science Liaison, Assistant Director Medical Affairs.
Dr. Veronique Pryce Carney serves as a Medical Science Liaison at TimKings International Associates. In this role she supports clinical trials, scientific engagement, medical strategy and building KOL relationships. Demonstrates clinical expertise across Oncology, Immunology, Dermatology and Rare disease therapeutic areas. She is committed to translating complex scientific data into clear, actionable insights that support evidence based patient care.
We encourage potential sponsors and stake holders who will want an expert conduct of their potential clinical trial studies with anticipated successful outcomes to outsource or delegate their studies to Timkings InternationalAssociates Limited and we will apply our expert knowledge to your potential studies as we are bent on achieving excelent Regulatory , Protocol Ethical Compliance Outcomes with deep ICH GCP Adherence to our sponsors . We promise to seemlesly run your trials with a team of Expert & Experienced Cinical Trial Staff with Current GCP Certifications and Excellent Regulatory Knowledge , from Start-Up Regulatory , Maintainance and Close Out, under strict Regulatory and Ethical Adherence , Master Plan of Budget Building, , Clinical Trial Protocol, Quality management Systems (QMS) & Audit & Academics, Regulatory Affairs, Ethics, & Compliance Support, Cinical Trial Protocol Design, Cinical Data and Biostatistics & Communications , Cinical Data Management ,Clinical Data Technology Enablement, Quality Management, SOP Development & Compliance Advising, Operational Consulting, Medical Writing & Scientific Communication ,EDC Build Services and Quality Management & GxP Compliance (SOP, Audit,CAPA) etc
To speak to one of our staff or to book appiontment , contact the company's email , timkingsinternationalassociates@timkintelclconsult.com or telephone +1(209)9731016.
Our Head Quater Address: Timkings International Associates Limited, 1311 Park ST , Unit 11427, Alameda , CA 94501 , USA.
DEDICATION/ PHARMA & CRO SERVICES
I Dedicate God Almighty "Jehovah", His Only Begotten Son Jesus Christ and The Holy Ghost as the owner of me, my family, this website, and Timkings International Associates Limited. Timothy Ekwebelem the CEO of Timkings International Associates Limited, a company built on Faith, Trust, Fear and Believe in God Almighty Jehovah and His Only Begotten Son Jesus Christ & Holy Ghost declares that JEHOVAH The Almighty God is the Only True Origin, Maker & The Creator of Medicine and Clinical Research
Guaranteed Industry Placement/Employment
Receive one-year paid placements/full time permanent position with our Timkings International Associates and other pharmaceutical companies or CROs upon course completion. The course/training only takes six weeks intensive /comprehensive professional clinical research training exposing you to teachings, course works, simulated practical reports, tutorials/ interactive sessions, presentations, quizzes etc. You are immediately placed on a fully paid one year placement that transition you to an automatic permanent position in our organization and many leading Pharma/Clinical Research Organizations. The completion of the training program leads to award of powerful Professional Certificate as a CRA. There are token fees to pay for the training and are classified into two categories, 1. Intensive/ comprehensive professional clinical research training (group) with work placement (Price) $3500 2. Intensive / comprehensive professional clinical research training private/one to one with work placement. (Price) $6000 This payment can be paid to this account. Account Holders Name: Timothy Chinyereugo Ekwebelem. Account Number: 211830029961. Wire Routing: 101019644. ACH Routing: 101019644. Account Type: Checking. Bank Name: Lead Bank. Bank Address: 1801 Main St., Kansas City, MO 64108 ;
Tailored Learning Opportunities
Choose between individual or group training modules to best suit your schedule and career aspirations. This training is tailored to suit your needs as we understand you go to work and will need the training after coming back from work and therefore, we tailor it to suit you and your needs and there are two types , intensive/comprehensive advance level training by group with automatic work placement and the intensive/comprehensive advance level training (private /one to one).The two routes of training are equally good, all depends on your choice of preference and availability for the training. We encourage those who are passionate about the career in clinical research, those who are devoted, self-motivated, focus and very decisive about their chosen career. Paying tuition fees does not guarantee employment in our organization rather, your interest, hard work, motivation and the ability to learn within a short period of time. We are practically oriented and practicals consitute 70% of what you are going tobe learning in our training institute. Our style of teaching is unique and different from what you see in other training organization. We give you the best ever world class training in clinical research, replacing experience in lue of your training. From the first day you start, you are pracytically trained as apprentice rather than academic as we are more practically oriented, giving you challenging practical and theoretical case studies, building you to learn by examples.
Comprehensive Clinical Research Training. Group- Price: $3500. Private -(one to one) Price: $6000.
Gain intricate knowledge and expertise in clinical and non-clinical drug development through our specialized online program. This program allows you to work while you are being trained. It is tailored to suit you while you are working. It is broken down into block of three days every week for six weeks. This means you must choose and complete three days in week for six weeks with intensive, rigorous comprehensive training with class teachings, course works, tutorials /interactive section, simulated practical and practical reports, presentations, quizzes etc. We are practical oriented, and the simulation practical prepares you for the real job of a CRA, hence teaching from scratch to finish everything about pre-clinical and clinical research believing you are a novice in the field even when you have a work experience. This training is designed with the focus of training clinical research professional with high level of industrialized curriculum with the concept of bringing practicality into reality basing all training to equip trainees to become independent and confidence in their clinical research profession. It doesn't matter if you want to start a fresh career in clinical research or you are a fresh graduate looking for experience or professional clinical research personnel trying to return back to work, the curtain is opened for all and sundry. We give you a standard industrial training in clinical research that no one else is willing to give you. We understand your pains, misery and agonies that's why we tailored this training not to involve interview to wipe away your tears. We don't believe in interviews therefore on the completion of the six weeks training you are automatically placed in either Timkings International Associates Limited or some of our partnering clinical research organizations and pharmaceutical companies. We have sixteen Pharma companies and eight CROs globally that are waiting to place you on automatic fully paid one year placement that will transition you into a permanent position after your placement. We need focused minded, decisive, hardworking, intelligent, serious-minded people in our organizations meaning we need you more than you need us. Token fees are paid depending on the type of program you want. We have two types of programs, the comprehensive /extensive professional clinical research group training with a token price of $3500. This is a one term payment which you can pay directly on this website. We also have the comprehensive/extensive clinical research training one to one (private) which cost $6000. We tailored it to suit your needs, and you are to choose between this two. Our training is 100% online and you can study and work from every part of the world. We also offer working visa sponsorship for our workers with medical insurance for you and your dependents with travel allowance. Let us throw away the old-fashioned interviews that restrict people and adopt training by learning and placement by permanent role. If you believe in this thought, then enroll now while it last. Contact the CEO on email timothyekwebelem@timkintelclconsult.com and phone number +1(209)9731016.
Tailored Work Placement According to Choice
Timkings International Associates Limited places successful trainees automatically to their chosen clinical research positions like CRA, CRC, CTA, CDM, Clinical Research Operations, Start-up Regulatory specialist, Regulatory Specialist, CTM, Project Manager, Line Manager, Dispense Pharmacist, PI, MD etc. All positions are automatic without interviews after the successful completion of the Professional Clinical Research Training Program. We also need professionals in different scientific field; we are going to train for our Research and Development Department as we explore and research on different studies that breakthrough in different scientific discoveries and scientific Innovation findings. We make use of artificial intelligence in all scientific and biological studies with leading experts leading in our current and future research in cardiovascular, hematology, sickle cell, neurology, neuropharmacology, oncology, Diabetes, hypertension, sickle cell, and using our expertise techniques with sophisticated computerized and advanced ultra-modern advanced technology that will give us breakthroughs in our clinical, pharmaceutical and medical research. We are leading experts in clinical research facilitating and giving the best techniques in our clinical research outcomes as expert contract research organization and pharmaceutical company. You made the best decision by joining our company Timkings International Associates Limited
PARTNERING
Timkings International Associates has open arms for international partnerships within its own organization in granting work placement and permanent remote employment to our trainee's staff students in Clinical Research endeavors. Timkings International Associates Limited placed trainees who have completed their six to eight weeks training, a permanent employment role in its organization offering employment to members on the condition that they successfully finish and complete their training program while still working for the company enabling them to gain work experience while undergoing the compulsory training. We are a company legally registered and incorporated on the company's allied matters ACT 2020 with a registration number 8461910, a private company limited by shares. Timkings International Associates Limited is working on different project ranging from wound care, HIV, microvascular, and hypertension. In HIV studies the company is working with important solvent and acetic acid to denature the integration of HIV RNA into the Host DNA. The protocol and study design of the project focused on using mice's and rat in learning how Acetic acid and important solvents can denature the HIV integration ability that stops HIV from being able to send coded RNA messages to the cell membrane of the host which directly paralyses HIV from its ability of sending their RNA massages to the cell membrane. If the coded messages of HIV RNA is stopped from transmitting its RNA coded instruction to the cell membrane , cell membrane will not be deceived to believe that this messages are coming from the host DNA, therefore will not be able to send RNA coded messages to Helper T Cells, B cells , C cells and the entire immunity of the host and other organs will not be infected with HIV virus, a possible cure for HIV endemic. If you or your team love what we do and want to be a part of the program/ studies/ project, please contact the company directly through the CEO'S email timothyekwebelem@timkintelclconsult.com or +1(209)973 1016 .We need sponsors that can partner with us in the Pre-clinical / Toxicological /Pharmacological stage even to the clinical trial stage .The project / Research Design / Protocols has been designed and written already though we cannot demonstrate the mechanism of reaction of our new therapy, here on website but we are seriously looking for sponsors ( pharmaceutical companies , government and private agencies) who might want to be our sponsors in partnership to contact the CEO of Timkings International Associates Limited Timothy Chinyereugo Ekwebelem a British trained Clinical Research Professionals that have worked with top British Professors in different therapeutics and publications in British recognized Medical Journals on his personal number +12099731016 or email him on timothyekwebelem@timkintelclconsult.com
HIV / DIABETIC / SICKLE CELL AND VENOUS ULCER STUDIES
Timkings International Associates limited is currently working on HIV therapeutics, Wound Care/ Diabetic Ulcers/ Venous chronic ulcers. Our studies in HIV/AIDs are focused on finding a permanent cure on HIV/AIDS and currently we are at the stage of pre-clinical animal toxicological studies to demonstrate how HIV can be denatured using some powerful solvent and acetic acid to attack HIV and denature it from integrating its RNA into Host DNA. The study is quite promising, and we are looking for sponsors and stake holders to partner and collaborate with us in developing these studies. Please contact us if by any chance you want to collaborate and partner with us.
RESEARCH AND DEVELOPMENT
Timkings International Associates Limited is a company well known for its Expert Research and Development Team from all parts of scientific field as a global team actively researching for new areas of medicine and clinical research using state of the art analytics or patient first solution to make research and clinical trials more accessible. We are currently developing new theories on different therapeutics in medicine, actively researching for possible cures in certain cancers and are potentially seeking cures for all forms of cancers, HIV new theories being developed in our Toxicological/pharmacological studies in pre-clinical trial stages. We have staffs professional clinical trial expert that are working expertly in cutting edge technology using artificial intelligence to predict outcome of clinical trial result by using efficient and quality standard in working and designing clinical research with well meaningful research design. We operate as a Pharmaceutical Company, a CRO and a Clinical trial consultancy with contracts focused on different phases of clinical research, hence we help Sponsor Organization plan their research design & protocol of their studies with excellent predictable quality outcome, adhering to all regulatory and ethical standards, with less cut business budgets and choosing the right expert clinical trial sites for your organization.
MASTER PLAN OF BUDGET / CLINICAL TRIAL RESEARCH PROTOCOLS
At Timkings International Associates Limited we overcome the complexity of intricate protocols, large enrollment requirements, global site networks and delivers demands. We build better study budgets while reducing costs and improving Start-Up times accurately and compliantly. We design your study, make excellent budget with anticipated risks, solve anticipated risks with solution to any challenging outcome risks that might occur in the future of your trial study. We budget to suit your expertly demand and with optimum standard and expert knowledge of regulatory application/submission in different therapeutics like Cardiovascular, Cell and Gene Therapy, Central Nervous System, GI & Hepatology, Infectious Diseases and Vaccine, Oncology and Hematology Pediatrics, and rare diseases including Sickle Cell SS.
Regulatory, Ethics & Document Readiness Support
Support services to help sponsors, investigators, and research teams prepare essential regulatory and ethics documentation with accuracy and efficiency. We assist with the creation and review of core study files, submission checklists, version control, and audit-ready documentation practices-helping you maintain quality and compliance from study start through close-out.
Quality Management, SOP Development & Compliance Advisory
Build or strengthen your Quality Management System with practical, implementation-focused guidance. We develop and improve SOPs, work instructions, templates, and training records, and provide compliance gap assessments to align operations with ICH-GCP and applicable local regulations. Ideal for organizations scaling into clinical research or seeking stronger internal governance.
Operational Consulting: Study Feasibility, Site Setup & Trial Execution Support
End-to-end operational consulting to help studies run smoothly and predictably. Our team supports feasibility planning, site selection criteria, activation timelines, communication plans, risk-based monitoring approaches, and issue management workflows-ensuring clear coordination between sponsors, sites, vendors, and internal stakeholders throughout trial execution.
Regulatory & Ethics Submission Support
We support sponsors and investigators with end-to-end documentation for ethics and regulatory submissions. Services include preparation and review of study start-up packages, informed consent documentation support, essential document QC, and readiness checks to align with ICH-GCP expectations and local requirements.
Clinical Data & Biostatistics Services
From database set-up to clean, analysis-ready datasets, we provide practical data services that strengthen study outcomes. Our team supports CRF review, data cleaning workflows, query management guidance, basic statistical planning support, and clear summary reporting designed for stakeholders and decision-making.
Medical Writing & Scientific Communication
We develop high-quality, audience-appropriate scientific content for research and healthcare organizations. This includes SOPs, study templates, training manuals, slide decks, manuscripts, and publication-ready materials-written with clarity, consistency, and compliance in mind.
Clinical Data & Technology Enablement
Strengthen data integrity and operational visibility through fit-for-purpose clinical trial technology support. We advise on EDC and eSource readiness, database setup considerations, CRF review support, and data workflow optimization, including query management standards and reconciliation planning. This service helps teams improve data quality, reduce avoidable rework, and enhance real-time oversight across clinical programs.
Regulatory Affairs, Ethics & Compliance Support
We help sponsors, sites, and emerging clinical teams navigate regulatory expectations with confidence. Our consultants provide guidance on ethics submissions, informed consent documentation, essential document readiness, inspection preparedness, and ongoing compliance processes-ensuring studies are conducted in alignment with ICH-GCP and local regulatory requirements. This service is designed to reduce avoidable delays, strengthen documentation quality, and standardize compliance across your research operations.
Regulatory & Ethics Submission Support
We help sponsors, investigators, and research teams prepare and submit high‑quality regulatory and ethics documentation across the clinical trial lifecycle. Our support covers informed consent documentation, essential documents, investigator files, GCP-aligned templates, and submission readiness reviews-designed to reduce avoidable queries and ensure clean, compliant packages for IRBs/IECs and national regulators.
Clinical Data Management & EDC Build Services
Timkings International Associates provides end‑to‑end clinical data management services-from CRF design and edit checks to EDC configuration, user training, data cleaning, and database lock. We apply robust data standards and clear data review workflows to improve data quality, speed up timelines, and strengthen inspection readiness for both early and late phase studies.
Quality Management Systems (QMS) & Audit Readiness
We support organizations in building and strengthening their GxP quality systems, including SOP development, CAPA management, risk-based quality planning, vendor qualification, and internal quality reviews. Our focus is practical: creating a QMS that teams can follow confidently while remaining aligned with regulatory expectations and inspection requirements.
Regulatory & Ethics Submission Support
We support sponsors and research teams through the end-to-end documentation required to initiate studies responsibly. Our specialists help assemble submission-ready packages for IRB/IEC review, competent authority filings, and essential document sets-ensuring consistency, completeness, and alignment with applicable guidelines and local requirements.
Clinical Data Services & Biostatistical Support
From database planning to clean, analysis-ready datasets, we help teams manage trial data with accuracy and traceability. Services include EDC build guidance, CRF design input, data validation strategy, query management workflows, data reconciliation, statistical analysis plans support, and results reporting assistance for scientific and regulatory use.
Quality Management & GxP Compliance (SOPs, Audits, CAPA)
Build a resilient quality system that scales with your research operations. We provide QMS design, SOP authoring and review, inspection readiness coaching, internal audits, vendor qualification support, deviation management, and CAPA planning-helping organizations strengthen compliance and operational control across GCP/GDP/GMP-related activities.
Regulatory & Quality Compliance Support
We help sponsors, startups, and research teams strengthen compliance across the clinical research lifecycle. Our specialists provide practical guidance on ICH-GCP alignment, essential document readiness, audit and inspection preparation, deviation/CAPA workflows, and quality management system (QMS) implementation-so your studies remain inspection-ready and operationally consistent.
Clinical Data, Pharmacovigilance & Medical Writing
Build high-quality evidence with integrated data and safety services. We support clinical data workflow design, query management practices, database documentation readiness, safety reporting processes, and professional medical writing for key study documents (e.g., protocol support content, reports, and structured narratives). Our goal is clear: accurate data, compliant safety handling, and documentation stakeholders can trust.
Study Start-Up & Site Activation Services
Accelerate study initiation with structured start-up support designed to reduce delays. We assist with feasibility planning, site selection workflows, document collection, CTA/contract coordination, ethics/IRB submission readiness, and activation checklists-ensuring teams move from concept to first-site-ready with clear timelines and accountability.
Oncology Clinical Trials
We are experts in conducting oncology clinical trials , with trained and experienced staffs who are focused on achieving the best results having the safety, interest and welfare of trial participants in heart , observing regulatory compliance and ethical adherence, we bring the best result outcome. From Start-up, Maintainance and Close out visit , we are there to make sure we deliver the best clinical outcomes and even help in publishing clinical trial results outcomes.
