Contact Yashira Consulting Services, LLC
Contact Details
Service Area: Bronx, NY (serving clients across the U.S.)
Business Hours: Monday – Sunday, 8:00 AM – 8:00 PM
We aim to respond to all messages within one business day.
Start Your Clinical Trial Journey with Expert Support
If you're planning, managing, or troubleshooting a clinical trial, Yashira Consulting Services, LLC is here to help. We provide personalized consulting services for biotech companies, pharmaceutical sponsors, CROs, academic research institutions, and community-based health organizations.
Our Bronx-based firm specializes in helping clients streamline trial execution, improve site performance, enhance recruitment outcomes, and maintain GCP and FDA compliance. Whether you’re launching your first study or managing a complex portfolio of trials, we offer the clarity, structure, and operational support your research deserves.
This page includes everything you need to know to reach out, schedule a consultation, and learn more about how we can assist your team.
What Happens When You Reach Out?
We want our first conversation to be as useful and productive as possible. When you contact Yashira Consulting Services, here’s what you can expect:
- Initial Response: We’ll respond via phone or email within 24 hours to gather a few more details about your inquiry.
- Consultation Scheduling: We’ll offer a free initial consultation (30–45 minutes) to learn more about your trial, your team, and your operational challenges.
- Needs Assessment: During the call, we’ll walk through your trial phase, resource capacity, and any roadblocks you’re facing—whether regulatory, operational, or recruitment-related.
- Follow-Up Plan: After our meeting, you’ll receive a summary of recommendations, a list of applicable services, and a clear next-step proposal for engagement.
Our process is always client-led, transparent, and no-pressure. We're here to add value—not sell services you don’t need.
Services You Can Inquire About
When you reach out, we can discuss any of the following areas:
- Clinical Trial Planning & Feasibility
- Clinical trial project management and staffing
- Study Startup Support
- Site Selection & Site Activation
- Participant Recruitment Strategy
- CRO/Vendor Oversight & Communication
- Regulatory Compliance & GCP Documentation
- Audit Preparation & QA Systems
- Workflow Optimization & SOP Development
- Diversity, Equity & Inclusion Integration
Our services are tailored to your needs, budget, and timeline—whether short-term project-based or long-term strategic support.
FAQs
Can I get help with a single aspect of my study (e.g., recruitment)?
Yes. We offer modular services and are happy to support specific pain points or functions.
Are you available for on-site support?
Yes. While we operate primarily remotely, on-site support can be arranged depending on project scope and location.
How much does consulting cost?
Our rates vary by project size and duration. After the consultation, we’ll provide a proposal with clear pricing and deliverables.
Do you work with teams outside New York?
Absolutely. We serve clients nationwide, and many of our engagements are fully remote.
Can you help us prepare for an FDA inspection?
Yes. We provide inspection readiness services, mock audits, SOP reviews, and staff interview preparation to ensure compliance.
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Who Should Contact Us?
We work with organizations across the research ecosystem, including:
- Biotech Startups: Need help with study planning, CRO selection, or IND readiness? We support early-stage teams without in-house clinical operations staff.
- Pharma Companies: Managing multiple trials and vendors? We help maintain oversight, compliance, and cross-functional coordination across departments.
- Academic Medical Centers: Launching an investigator-initiated study? We can assist with protocol development, IRB navigation, and operational planning.
- Contract Research Organizations (CROs): Need support managing sponsor expectations or trial performance? We bring an objective perspective and experience coordinating cross-functional stakeholders.
- Nonprofit or Community-Based Research Programs: Trying to reach underrepresented populations or build trust in diverse communities? We specialize in community engagement strategies that are ethical, inclusive, and practical.
If you’re working in or around clinical research, and need operational, strategic, or compliance guidance, we can help.
Why Clients Work With Us
Yashira Consulting Services, LLC is led by Yashira Henriquez, a clinical operations expert with experience at both academic and industry-leading organizations. Clients choose to work with us because:
- We understand the complex realities of trial operations, not just theoretical best practices.
- We bring experience managing studies at institutions like Yale School of Medicine and Regeneron Pharmaceuticals.
- We provide bilingual (English/Spanish) services for inclusive communication and outreach.
- We design practical SOPs, timelines, and workflows that align with your team’s size and scope.
- We operate with integrity, responsiveness, and respect for your team’s mission.
We take pride in offering responsive, ethical, and personalized consulting that adapts to the evolving demands of your trial.
Let’s Talk About Your Trial
Whether you're facing delays, unsure where to start, or just need a fresh set of eyes on your current operations, we're here to help. Yashira Consulting Services, LLC brings thoughtful strategy and efficient execution to every partnership.
