Frontage Laboratories·Secaucus, New Jersey
The coordinator is responsible for planning and implementing clinical research trials, including performing medical procedures and managing study data. They also maintain regulatory documentation and liaise between the Principal Investigator, sponsors, and the IRB.
Title: Clinical Research Coordinator
Frontage Clinical Services, Inc. in Secaucus, NJ
Reports to: Manager of Clinical Operations
Frontage Laboratories Inc. is an award winning, publicly listed (HKSE), full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China, and growing over 30% YOY. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.
Responsible for working under the guidance of the Principal Investigator and Sub-Investigators, and Clinic Operations to participate in the planning, implementation and overall direction of clinical research trials conducted on behalf of sponsors at the Frontage Clinical Services, Inc. The Clinical Research Coordinator is required to perform study procedures, to generate, evaluate, review and record study data, to transcribe source data to case report forms, to liaise with sponsor personnel, to maintain a high level of professional expertise through familiarity with the study protocol, investigator's brochure, and related study materials, and to participate in project team meetings. The Clinical Research Coordinator II assists the Principal Investigator in conducting clinical research studies in compliance with applicable regulations and GCP guidelines.
$50K - $52K annual salary
Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.
A bachelor's or master's degree in biology, chemistry, or a related field is preferred, along with a desire for at least one year of clinical research experience. Candidates must have solid knowledge of GCP and FDA regulations and strong organizational skills.
Market context
Clinical Research Coordinator roles in New Jersey are often tied to hospitals, academic medical centers, and oncology research sites, where demand can be steady for candidates who understand trial operations and compliance. This role is competitive because employers typically want prior clinical research experience, GCP knowledge, regulatory familiarity, and comfort with Phase 1 oncology work; review the AI-summarized requirements and benefits here to save time before applying. A practical next step is to tailor your resume to highlight GCP, regulatory documentation, and Microsoft Office experience, plus any oncology trial exposure.