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For Clinical Trial Investigators
Use your medical expertise to help evaluate new treatments, expand access to clinical trial opportunities, and contribute to the future of patient care.Triallogix works with experienced and first-time clinical trial investigators who are interested in conducting high-quality research with a strong focus on participant safety, regulatory compliance, and reliable study execution.
20+ Years Combined Experience
Decades of real-world research experience that guides every study
Robust Clinical & Regulatory Team
Clinical, regulatory, and operational expertise under one roof
Full-Service Support
Staff, training, recruitment, operations, and more—all in one place.
What does a Principal Investigator do?
A principal investigator, commonly called a PI, is the qualified medical professional responsible for the conduct of a clinical trial at a research location.
The PI oversees the study team, protects the rights and safety of participants, and helps ensure that the study is conducted according to:
- The approved research protocol
- Good Clinical Practice principles
- Sponsor requirements
- Institutional review board or ethics committee requirements
- Applicable laws and regulations
- Approved informed consent documents
- Site policies and study procedures
Clinical research coordinators and other trained personnel may manage many day-to-day study activities, but the principal investigator retains overall responsibility for the trial at the site.
Protect Patient Safety and Welfare
Prioritize the rights, safety, and well-being of every participant through consistent medical monitoring
Adhere To Research Protocol & Regulatory Guidelines
Ensure compliance with study requirements
Review Study Documentation
Maintain high-quality clinical documentation along with review of subjects’ charts and ongoing health
How Triallogix Supports Investigators
Clinical research is one of the few revenue lines a private practice can add without seeing more patients. The barrier has never been interest — it's infrastructure. Triallogix contracts directly with private physician offices and brings the entire operation with us: our coordinators, our equipment, our regulatory systems, our recruitment engine. Your staff keeps doing their jobs. You become a Principal Investigator.
Not every study is appropriate for every investigator. We focus on evaluating fit before encouraging a physician to pursue an opportunity. Study availability and investigator selection ultimately remain subject to sponsor approval, protocol requirements, geographic needs, and site qualification.
We’re proud to offer:
Trial Identification
We identify and apply for research opportunities aligned with your specialty and patient population on your behalf
Feasibility Support
We’ll evaluate study fit, patient population, and site readiness prior to study start and assist with site feasibility forms
Site Initation Preparation
Ensure your site is fully prepared for a successful study launch
Investigator Onboarding
We’ll give a complete walk through of investigator responsibilities and training required
Complete Staffing
Access experienced clinical research coordinators and research trained R.N.s and M.A.s to support every stage of your study
Research Workflow Development
We’ll create efficient workflows between existing staff and research staff that keep study visits organized
Source Documentation Development
We’ll create efficient workflows between existing staff and research staff that keep study visits organized
Regulatory Document Oversight
we help keep essential regulatory documentation organized, accurate, and inspection-ready
Subject Recruitment Strategy
We develop targeted recruitment plans to identify and enroll qualified participants
Monitoring Visit Support
We offer guidance in preparing for sponsor monitoring visits with organized records
Query Resolution Support
We help resolve sponsor data queries quickly to keep studies moving forward
Quality Review
Our research professionals will identify potential issues early through proactive quality and compliance reviews throughout the study
Closeout Preparations
We allow your site to complete final documentation and study requirements with confidence
Triallogix Brings
Study identification and sponsor outreach
Contract and budget negotiation
Dedicated research coordinators on our payroll
All study-related equipment
Regulatory submissions, IRB correspondence, and document management
In-house recruitment marketing and enrollment support
Your Practice Keeps
Your existing schedule and patient flow
Your staff, doing their existing jobs
Zero additional HR, hiring, or turnover exposure
Your capital, uncommited
Your clinical judgement and PI authority
Your patient relationships
Frequently
Asked Questions
Curious about becoming a PI but unsure of what it entails? Here are some of the most common things people want to know before they join our team.
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Meet Our Investigator Team
Kevin Oei, D.O.
Principal Investigator
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Arjun Makam, D.O.
Principal Investigator
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Darren Knight, M.D.
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Joanna Chan, M.D.
Principal Investigator
Anand Trivedi, M.D.
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Judith Bedoy, M.D.
Principal Investigator
Michael Maidaa, M.D.
Principal Investigator
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Alexa Chai, M.D.
Principal Investigator