Clinical Research Coordinator I
Union, NJFull-time$22–23/hrSeen 1 day agoSeen in employer's feed 1 day ago
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At a glance
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Job overview
SGS North America is seeking a Clinical Research Coordinator I to coordinate and conduct clinical studies, manage study documentation and materials, and support study teams in following protocols, SOPs, regulations, and Good Clinical Practice guidelines. The role includes coordinating subject visits, resolving queries, monitoring panelist compliance, and handling study-specific tasks. Candidates need an associate degree or an alternative combination of relevant work experience and a GED or high school diploma.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
Compensation
$22.00 - $22.00 / Hourly
Hours Per Week
40
Number Of Positions
1
Job Description
Full-time
Compensation: USD 22 - USD 23 - hourly
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.
Job Description
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
Qualifications
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.
Additional Information
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.
Health: Medical, dental and vision insurance, life insurance, employee wellness programs
Wealth: Competitive pay, 401(k) with company match (immediate vesting upon enrollment), employee referral program, annual bonus target
Happiness:
Professional Growth: Online training courses, virtual and classroom development experiences, tuition reimbursement program
Work-Life Balance: Paid-time off (vacation, sick, company holidays, floating holidays, volunteer time)SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required.
This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time.
If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call 201-508-3149 for assistance and leave a message. You will receive a call back. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.
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Job Location
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Apply here: https://www.aplitrak.com/?adid=YmJnZW5lcmljLjc1ODg5LjEwNDEyQHNnc25vcnRoYW1lcmljYWNvbXAuYXBsaXRyYWsuY29t
Place of Work
On-site
Requisition ID
744000161087239-5842
How this job compares
Set against the 626 open Clinical Research Coordinator jobs on Olive Jobs, counted November 14, 2026.
- Pay
- This posting$22–23/hr
- US median$25–38/hr202 hourly ranges
This range's midpoint, $22.50/hr, is 25% below the US median midpoint ($30/hr) — in the lowest quarter of Clinical Research Coordinator hourly ranges across the US.
- Openings
- Olive Jobs lists 19 open Clinical Research Coordinator jobs in New Jersey and 626 across the US. 1% of them nationwide are listed as remote or flexible.
- Hiring the most across the US
- Actalent43 open
- Mount Sinai Health System43 open
- Iterative Health37 open
- Experience
- Clinical Research Coordinator postings that state a minimum ask for 2 years of experience at the median; the middle half ask for 1 to 3 years (423 postings).
- Education
- 184 of the 626 open Clinical Research Coordinator jobs (29%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on November 14, 2026. Figures based on too few postings are left out.
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