Bilingual APRN / Nurse Practitioner

About 3Sync Research

3Sync Research is a growing clinical research organization dedicated to advancing medicine through high-quality clinical trials. We partner with leading pharmaceutical companies, CROs, physicians, and healthcare professionals to bring innovative treatment options to diverse patient populations.

Our office conducts outpatient clinical research across multiple therapeutic areas, including primary care, pediatrics, asthma/allergy, diabetes, endocrinology, infectious disease, vaccines, and other adult and pediatric studies. We are looking for a strong, experienced provider who is comfortable working directly with patients and supporting clinical trial oversight.

Position Overview

We are seeking a bilingual APRN / Nurse Practitioner to join our clinical research team as a Clinical Trial Sub-Investigator. This is an excellent opportunity for an experienced provider who is detail-oriented, and comfortable working with both adults and children.

In this role, you will work closely with the Principal Investigator, site directors, operations leadership, recruitment team, clinical research coordinators, sponsors, CROs, and regulatory teams to support the safe and compliant conduct of clinical trials. The Sub-Investigator will conduct patient screening, eligibility review, physical exams, safety assessments, protocol compliance, clinical documentation, enrollment support, participant retention, and contribute to overall site performance.

Key Responsibilities

Assist the Principal Investigator in the oversight and execution of clinical trials

Conduct patient screening, enrollment, and ongoing study visit assessments

Perform physical exams and clinical evaluations for adult and pediatric participants

Review medical history, medications, labs, vitals, inclusion/exclusion criteria, and study eligibility

Monitor participant safety throughout the study

Identify, assess, document, and report adverse events and clinical concerns

Perform or assist with blood draws, vital signs, and other protocol-required procedures

Review informed consent forms, source documents, lab reports, CRFs, and study records for accuracy and completeness

Support protocol compliance, data collection, and audit readiness

Communicate professionally with participants, parents/guardians, study staff, sponsors, CROs, and regulatory teams

Supervise and support clinical research staff when needed

Collaborate closely with site directors, operations leadership, recruitment teams, coordinators, and the Principal Investigator to support successful study outcomes, strong enrollment, participant retention, protocol compliance, and overall site performance

Serve as a team player within a fast-paced clinical research environment, helping ensure smooth communication between clinical, operational, and recruitment staff

Ensure study activities are conducted in compliance with FDA regulations, ICH-GCP guidelines, HIPAA, protocol requirements, and site SOPs

Requirements

Active and unrestricted License/Certification- Florida APRN / Nurse Practitioner License required

Minimum of 5+ years of experience as an APRN / Nurse Practitioner

(Bilingual English/Spanish )

Must be comfortable working with both adult and pediatric patients

Strong clinical assessment, documentation, and decision-making skills

Experience with patient evaluation, medical history review, medication review, labs, and clinical procedures

Phlebotomy or blood sampling experience preferred

Familiarity with medical terminology, clinical documentation, and outpatient patient care

Ability to work independently while collaborating with the Principal Investigator and research team

Strong attention to detail and ability to work in a fast-paced clinical environment

Professional, dependable, organized, proactive, and team-oriented

GCP certification preferred; training can be provided if needed

Availability to work occasional weekends as needed based on study requirements

Preferred Experience

Family Medicine

Primary Care

Pediatrics

Internal Medicine

Urgent Care

Allergy / Asthma

Endocrinology

Diabetes Care

Infectious Disease

Vaccines

Clinical Research

Clinical Trial Sub-Investigator experience

Ideal Candidate

The ideal candidate is an experienced, bilingual provider who is comfortable making clinical assessments, asking the right questions, identifying safety concerns, and working with a wide range of patients. We are looking for someone who is confident in their clinical judgment, reliable, personable, and able to take ownership of patient evaluations in a research setting.

This person should also be a strong team player who works well with site directors, operations leadership, recruitment teams, coordinators, and the Principal Investigator to help drive successful study outcomes, strong enrollment, participant retention, protocol compliance, and overall site performance.

Why Join 3Sync Research

Opportunity to work on innovative clinical trials and emerging treatments

Adult and pediatric patient population

Growing research organization with expanding study opportunities

Collaborative team environment

Exposure to multiple therapeutic areas

Flexible schedule available

Meaningful role in supporting patient safety and advancing clinical research

Benefits:

Health insurance

Dental insurance

Vision insurance

Paid time off

Pay: $88,117.74 - $106,120.29 per year

Benefits:

• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Work Location: In person