Clinical Research Coordinator I

SGS; Richardson (TX); On-site; USD 45,000 - 60,000; Full time

Job summary

SGS in Richardson, Texas is seeking a Clinical Research Coordinator I (CRC I) to lead studies and perform essential tasks. Responsibilities include coordinating studies, ensuring compliance with GCP, and performing data-related tasks.

The ideal candidate will possess an associate degree or relevant experience, with skills in research and project management. This role requires multitasking and adherence to study protocols.

Qualifications

• Ability to understand clinical research concepts and fulfill duties during clinical studies.
• Capable of managing and coordinating multiple projects in a fast-paced environment.

Responsibilities

• Lead coordinator on studies and execute follow-up visits.
• Perform daily tasks including document review and data entry.
• Coordinate and execute projects while adhering to GCP guidelines.

Skills

Language Skills

Mathematical Skills

Reasoning Skills/Abilities

Computer Skills

Project Management

Education

Associate degree or 2 years minimum of relevant work experience with GED or High School Diploma

Job 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.

By clicking the link above or any third-party link within this posting, you are leaving this site and going to a third-party website where the third-party website's terms and privacy policy apply