Senior Clinical Research Coordinator II: Study Ops

SGS

Richardson (TX)

On-site

USD 55,000 - 75,000

Full time

14 days+

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Job summary

SGS in Richardson, TX is seeking a Clinical Study Coordinator to coordinate and facilitate daily activities in clinical studies in accordance with protocol, GCP, SOPs and applicable regulations.

You will set up studies, prepare and organize study documentation, manage subject scheduling, assist IRB submissions, mentor new clinic staff and coordinate cross‑functional meetings with QA and Statistics to ensure smooth study operations.

Qualifications

  • Bachelor’s degree – preferably in science or other equivalent degree.
  • Understands basic concepts in clinical research and capable of learning and performing duties during clinical studies.
  • 2+ years relevant work experience

Responsibilities

  • Sets up and conducts study in compliance with protocol, SOPs, applicable regulations and GCPs
  • Prepares, completes, organizes and maintains all study documentation forms
  • Coordinates scheduling subjects for visits
  • Assists in training and mentoring new clinic staff
  • Prepares for and conducts pre-study meetings and other meetings as deemed necessary by management
  • Reviews and provides feedback on draft protocols, recruiting materials, and draft clinical study reports
  • Coordinates scheduling subjects for visits
  • Responds to queries from Quality Assurance and Statistics departments
  • Provides excellent customer service to clients and panelists and maintains a positive and respectful interaction with peers and supervisors.

Skills

Clinical research concepts

Education

Bachelor’s degree in science

Job description

SGS in Richardson, TX is seeking a Clinical Study Coordinator to coordinate and facilitate daily activities in clinical studies in accordance with protocol, GCP, SOPs and applicable regulations.

You will set up studies, prepare and organize study documentation, manage subject scheduling, assist IRB submissions, mentor new clinic staff and coordinate cross‑functional meetings with QA and Statistics to ensure smooth study operations.

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