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SPM Clinical Research Consulting LLC delivers specialized consulting services across the full lifecycle of Phase I–IV clinical trials. We provide end-to-end support from study start-up through close-out, including protocol development, operational oversight, regulatory strategy, budget development and contract negotiation, quality systems implementation, and data management solutions.


Every engagement is personally overseen by senior experts—ensuring consistent, high-quality guidance without the hand-offs typical of larger organizations. We combine deep regulatory expertise with a personalized consulting approach, committed to ethical research, patient safety, and delivering reliable results that advance your clinical development goals.

SPM Clinical Research Consulting is led by Susana Perez Martinez, PhD, Founder and Principal Consultant. All client engagements are personally overseen and executed by Dr. Perez, ensuring a high level of scientific expertise and consistency across projects.
As needed, SPM Clinical Research Consulting collaborates with a trusted network of external specialists to support specific project requirements.
To provide expert, customized clinical research advisory services that support the ethical, scientifically rigorous, and operationally sound conduct of clinical trials.
We are committed to advancing high-quality research through regulatory excellence, strategic execution, and data integrity—with the ultimate goal of improving patient outcomes and advancing medical innovation.


Commitment to quality, efficiency, and reliable results
Expertise across Phase I–IV clinical trials
Personalized, hands-on consulting approach
Strong regulatory compliance and quality focus
Proven experience supporting sites, CROs, and sponsors
Commitment to ethical research and patient safety
Scalable services tailored to each client's needs

Expert guidance, one conversation away.