SGS·Union, New Jersey
The Clinical Research Coordinator I serves as a lead coordinator for studies, managing daily tasks such as data entry, document review, and test material preparation. They ensure all study activities are conducted in compliance with GCP guidelines, SOPs, and specific study protocols.
Company Description We are SGS – the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.
Responsibilities include but are not limited to being lead coordinator on a study, executing follow-up visits ongoing studies, query resolution and other study specific tasks. The CRC I will perform daily tasks such as document review, data entry, test material preparation and data collection. This position may coordinate and execute projects assigned by the Clinic Manager while abiding by Good Clinical Practice (GCP) guidelines. JOB FUNCTIONS Performs station and instrumentation duties on other studies as assigned, including the collection and recording of clinical information Responds to queries from Quality Assurance and Statistics departments Sets up and conducts study in compliance with protocol, SOPs, applicable regulations and GCPs Prepares for and conducts pre-study meetings as well as other meetings and processes as deemed to protocol, SOPs and GCPs Monitor Compliance of panelists Prepares and is accountable for all Test Material for managed studies Adheres to study budget Prepares, completes, organizes and maintains of all study documentation forms, including drafting protocol amendments, case report forms, Electronic Data Capture (EDC), and other study specific documents Assures that staff working on their managed studies understand and are performing duties according to protocol, SOPs and GCPs Coordinates scheduling subjects for visits Completes other duties or tasks assigned by Clinic Manager and/or Supervisor JOB COMPLEXITY Multi-tasking is key IMPACT OF DECISIONS Make decisions as a study leader ANALYTICAL THINKING/PROBLEM SOLVING Handle issues with panelists and create solutions Arrange work for studies
EDUCATION AND EXPERIENCE Associate degree or 2 years minimum of relevant work experience with a GED or High School Diploma. Understands basic concepts in clinical research and capable of learning and performing duties during clinical studies KNOWLEDGE / SKILLS / ABILITIES Language Skills Mathematical Skills Reasoning Skills/Abilities Computer Skills Ability to manage and coordinate multiple projects in a fastpaced, highly professional environment.
Salary: $22.00 - $23.00/Hour Our Benefits We care about your total well-being and will support you with the following, subject to your location and role.
USD 22 - USD 23 - hourly
Candidates must have an associate degree or at least 2 years of relevant work experience with a high school diploma. A basic understanding of clinical research concepts and the ability to manage multiple projects in a fast-paced environment are required.
Market context
Operations roles in New Jersey often see steady demand in settings that support daily service delivery, especially when reliability, scheduling, and compliance matter. These positions can be competitive because employers often look for candidates who already hold CPR/First Aid certification, have a high school diploma or GED, and can work well with seniors. Review the AI-summarized requirements and benefits here to save time, then confirm your certifications and highlight any senior-care experience before applying.