Research Training
At Benchmark Clinical Research NJ, training is at the heart of our commitment to patient safety and research quality. Every member of our team receives rigorous, ongoing instruction to ensure the highest standards of care, compliance, and scientific accuracy. By investing in education, we build a culture of excellence that benefits patients, sponsors, and the wider community.
Our Training Standards
Benchmark Clinical Research NJ operates on a “no shortcuts” standard. Every staff member is qualified, protocol-ready, and routinely evaluated for competency. New personnel complete role-specific onboarding before handling any study tasks, and all team members participate in ongoing compliance, safety, and documentation training. Continuous education ensures every procedure is done correctly, the first time, every time. That’s how we protect patients, earn sponsor trust, and deliver dependable results.
Research Systems
Hands-on training in Electronic Data Capture (EDC), Clinical Trial Management Systems (CTMS), and Interactive Voice/Web Response Systems (IVRS).
Why Training Matters
Quality research depends on well-trained professionals. Our ongoing training ensures that patients are protected, data is reliable, and studies are conducted ethically. Sponsors and CROs can trust that every member of our team is prepared to deliver with accuracy and care, while patients can feel reassured that they are in safe, capable hands.
Access to Resources
We are developing a secure area where staff can access updated training materials, SOP manuals, and certification links. This ensures our team has the latest resources at their fingertips and provides sponsors with confidence in our commitment to compliance.
Our Commitment
Training is not a one-time requirement but an ongoing process. As medical research evolves, so does our dedication to continuous learning. By blending compassion, cultural awareness, and scientific precision, we ensure that our team is equipped to deliver meaningful contributions to medicine while always putting patients first.
A clinical trial is a carefully designed medical study that helps researchers test new treatments, medicines, or approaches to improve health. Trials follow strict safety rules and are reviewed by experts to protect patients.
Each study has its own requirements, such as age, medical history, or condition. Our team will review these with you and let you know if you qualify.
Yes. Your safety is our top priority. All studies follow strict guidelines set by the FDA and international research standards. You will be monitored closely by trained medical staff at every step.
Not always. Many patients come to us directly, while others are referred by their doctor, a caregiver, or our sister Internal Medicine and Pediatrics clinic.
You will meet with our research staff, who explain the study in simple terms and answer all your questions before you join. You may have health check-ups, monitoring visits, or questionnaires, depending on the study.
You are free to stop participating at any time. Your decision will not affect your regular medical care or relationship with our clinic.
We are located at 34 Union Avenue, Irvington, NJ. Our site is modern, fully equipped, and designed to provide both comfort and high-quality research.
You can call us, email us, or use our website to contact our team. We will guide you through the next steps and help determine if a study is right for you.
You can refer a patient by contacting our team directly by phone or email. Our staff will follow up with the patient, explain the study in detail, and guide them through the next steps.
Basic patient details such as name, contact information, and medical condition are usually enough to begin. Our research staff will handle the screening process and confirm eligibility based on the study requirements.
Not necessarily. Many studies allow patients to continue their standard care while taking part. Our research team will review all details with both the patient and their provider to ensure safety.
All studies follow FDA regulations, Good Clinical Practice (GCP), and strict safety protocols. Patients are monitored closely by our trained staff, and any concerns are addressed immediately.
We work with a diverse patient population, including individuals referred from our sister Internal Medicine and Pediatrics clinic, private practices, and a growing database of more than 2,500 patients. Each trial has specific criteria, so we review every referral carefully.
Yes. We value collaboration with referring physicians and can provide updates as needed, while always maintaining patient confidentiality and following HIPAA guidelines.
No. Participation is free, and in some studies patients may receive compensation for their time and travel.
We combine quality, dedication, and innovation to deliver reliable results and compassionate care. By partnering with us, you help patients gain access to promising new therapies while contributing to meaningful medical progress for the community.