We hear you! That's why we've founded Clinical Trial PM – a game-changing Project Management Company ready to support your Clinical Research Studies.
Gone are the days of grappling with delays, inefficient startups, and poor communication. With Clinical Trial PM as your dedicated partner, you'll unlock a seamless approach to managing studies. From collaborating with other Clinical Research Vendors to win new study awards, to assisting CROs and Sponsors to ensure timely project delivery, our team of seasoned experts will work closely to support clinical trial documentation, resourcing, audits, protocol changes, enrollment or other quality or project management tasks needed for your clinical studies.
Our mission at Clinical Trial PM is to champion high-quality, patient-centric clinical trials. We are dedicated to safeguarding patient safety, fostering transparency, and nurturing collaboration among all stakeholders. Our commitment is to train a diverse workforce in the art of managing clinical trials with a resolute patient-first approach.
Our vision is to be a preferred Clinical Project Management partner for Pharmaceutical, Biotech and Clinical Research Organizations making significant contributions to the advancement of Research. We aspire to set the gold standard for quality Clinical Project Management Services in the industry. By empowering a diverse and highly skilled workforce, we aim to enhance patient experiences, advance medical research, and build a future where innovation and compassion intersect seamlessly. We believe in a world where every clinical trial embodies the values of patient first, transparency, and collaboration.
We have developed a unique and effective business formula that ensures the seamless management of Clinical Research Studies, delivering excellence and value to our clients. Our formula encompasses the following key components:
Thorough Project Planning: Our experienced team starts by creating comprehensive project plans tailored to each clinical research study. This plan outlines clear milestones, deliverables, and timelines, serving as a roadmap for the entire project.
Meticulous Budget Management: We prioritize financial efficiency by overseeing and optimizing the budget throughout the study. Our financial analyst closely monitors expenses, ensuring resources are allocated wisely and cost-effectively.
Efficient Resource Allocation: We understand the importance of allocating resources effectively. Our support team, including the project manager, project assistant, and medical liaison, collaborates to ensure that the right expertise is assigned to each aspect of the study, maximizing productivity.
Proactive Timeline Oversight: Meeting deadlines is crucial in clinical research. Our team diligently tracks project timelines, identifying potential delays early on and taking corrective action to keep the study on schedule.
Rigorous Quality Management: Quality is at the core of everything we do. Our dedicated quality specialist implements strict quality control measures to uphold data integrity, accuracy, and compliance with regulations.
Dr. Tamiera S. Harris is the founder & CEO of Clinical Trial PM. She is a Clinical Research Executive with over 23 years of experience in Research and Clinical Trial Management. Dr. Harris is a Project Delivery expert with experience directing the overall planning, implementation, and completion of regional/global cross-functional projects adhering to SOPs, GCP, ICH, study timelines, contracts, and large Multimillion dollar budgets.
Dr. Harris has overseen Clinical Trials for five of the nation's leading ten Clinical Research Organizations throughout her career, including IQVIA, Parexel, PRA Health Sciences, PPD, and ICON. She has experience leading accounts for Pfizer, Novo Nordisk, Novartis, Roche, AstraZeneca, Amgen, GSK, Merck & Co, Incyte & Jazz Pharmaceuticals. Dr. Harris is driven by her belief in the transformative power of clinical research in saving lives. She has made it her mission to provide a comprehensive suite of Project Management services and trains a diverse global workforce to do the same. She is passionate about Clinical Research and enjoys speaking at conferences, planning Investigator meetings, training and supporting her team and clients.
The project manager is the key orchestrator, overseeing the entire study and ensuring seamless coordination between team members and stakeholders.
The project assistant provides valuable administrative support, ensuring documentation is organized, communication is streamlined, and logistics are efficiently handled.
Our medical liaison bridges the gap between medical expertise and project management, offering valuable insights and ensuring clinical integrity throughout the study.
The quality specialist is responsible for maintaining the highest standards of quality in data collection, analysis, and reporting, safeguarding the integrity of the research.
Our financial analyst meticulously monitors the study's budget, optimizing resource allocation, and providing financial insights to enhance cost-effectiveness.
Our commitment is to enhance the success of your Clinical Trials by offering a comprehensive suite of services tailored to your unique needs. With our guidance, you can navigate the dynamic landscape of Clinical Research with confidence, knowing that you have a seasoned team by your side.
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Schedule a consultation with Clinical Trial PM today and let's embark on this transformative journey together! Please note Consultations are $475 for up to an hour. We are a solution focused provider, that understands the value of time. We want to ensure each client and every inquiry provides an opportunity to learn and explore options to support your studies. This allows us to focus on supporting clients who are ready to explore all options to support their studies. If you are looking for Clinical Project Management training for your teams, study rescue support or coverage for a PM leave of absence, please specify in your inquiry.
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