Sgs Technologie LLC
Clinical Research Coordinator I
Richardson, TX, United States
Stay score
odds of building a lasting career here
Thin sponsorship signal and lottery-bound. A low-probability bet with your clock running. Prioritize cap-exempt roles and proven entry-level sponsors first.
Lottery odds assume a STEM candidate.
Personalize to your clock →Employer immigration record
from this employer's Department of Labor filings
Third-party placement is common here
Files H-1B transfers
Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.
Community outcomes
No reports yet — be the first to help the next applicant.
About the role
- Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.
- This position may coordinate and execute projects assigned by the Clinic Manager while abiding by Good Clinical Practice (GCP) guidelines.
- Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time.
Requirements
- Associate degree or 2 years minimum of relevant work experience with a GED or High School Diploma.
Skills
- Language Skills
- Mathematical Skills
- Reasoning Skills/Abilities
- Computer Skills
Company info
- 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
- Multi-tasking is key
- Make decisions as a study leader
- Handle issues with panelists and create solutions
This listing is sourced directly from Sgs Technologie LLC's careers page and normalized into a canonical job model.