SGS

Clinical Research Coordinator I

Posted 5 Days Ago

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Richardson, TX, USA

In-Office

Junior

Information Technology • Professional Services • Security • Consulting

The Role

Coordinate and lead assigned clinical studies including participant scheduling, data entry, EDC/CRF preparation, test material management, compliance with protocol/SOPs/GCP, query resolution, and study documentation. Support Clinic Manager and ensure staff follow study procedures.

Summary Generated by Built In

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

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.

Skills Required

Associate degree OR 2 years relevant work experience with GED or High School Diploma
Understanding of basic clinical research concepts and ability to perform study duties
Familiarity with Electronic Data Capture (EDC), case report forms, and data entry
Knowledge of Good Clinical Practice (GCP) and Standard Operating Procedures (SOPs)
Strong organizational, multi-tasking, and project coordination abilities
Computer skills (for data collection and documentation)
Ability to respond to QA and statistics queries and maintain complete study documentation

SGS Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about SGS and has not been reviewed or approved by SGS.

Healthcare Strength — Core medical, dental, and vision coverage is part of the U.S. package and is generally viewed as adequate even if not standout. Company information also underscores healthcare coverage as a standard element of the offering.
Retirement Support — A 401(k) is commonly included in the U.S., and group disclosures reference post‑employment benefit plans in select regions. These components provide a baseline of retirement security beyond core pay.
Strong & Reliable Incentives — Annual incentive/bonus structures are part of the compensation mix and cited positively in some regions and roles. Punctual pay is also highlighted as a plus.