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Clinical Research Coordinator I

SGS

Union, NJFull-time$22–23/hrPosted 1 day agoStill listed today

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At a glance

Compensation
$22–23/hr
Location
Union, NJ
Schedule
Full-time
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Job overview

SGS seeks a Clinical Research Coordinator I to coordinate and conduct clinical studies, including follow-up visits, query resolution, documentation, data collection, and test material preparation. The role may coordinate projects assigned by the Clinic Manager and requires compliance with study protocols, SOPs, applicable regulations, and Good Clinical Practice guidelines. The coordinator also schedules subject visits, supports study staff, and handles panelist issues.

Skills & qualifications

RequiredNice to have

Skills

Clinical Research, nice to haveLanguage Skills, nice to haveMathematical Skills, nice to haveReasoning Skills, nice to haveComputer Skills, nice to haveProject Coordination, nice to haveMultitasking, nice to have

Qualifications

Associate Degree or 2 Years Relevant Work Experience With GED or High School Diploma, nice to have

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match
Tuition Assistance
Paid Time Off

Full job description

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.

How this job compares

Set against the 622 open Clinical Research Coordinator jobs on Olive Jobs, counted November 12, 2026.

Pay
  • This posting$22–23/hr
  • US median$25–36/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 622 across the US. 2% of them nationwide are listed as remote or flexible.
Hiring the most across the US
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 (417 postings).
Education
186 of the 622 open Clinical Research Coordinator jobs (30%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on November 12, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.

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