Clinical Research Coordinator I
SGS · Richardson, TX · 2 wk ago
On-siteResearchFull-time
Responsibilities
- Lead coordination on a study
- Execute follow-up visits for ongoing studies
- Resolve queries from Quality Assurance and Statistics departments
- Set up and conduct study in compliance with protocol, SOPs, applicable regulations, and GCPs
- Prepare for and conduct pre-study meetings as well as other meetings and processes as per protocol, SOPs, and GCPs
- Monitor compliance of panelists
- Prepare and be accountable for all Test Material for managed studies
- Adhere to study budget
- Prepare, complete, organize, and maintain all study documentation forms, including drafting protocol amendments, case report forms, Electronic Data Capture (EDC), and other study-specific documents
- Affirm that staff working on their managed studies understand and perform duties according to protocol, SOPs, and GCPs
- Coordinate scheduling of subjects for visits
- Complete other duties or tasks assigned by Clinic Manager and/or Supervisor
Qualifications
- 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
- Knowledgeable in language, mathematical, reasoning, computer, and ability to manage and coordinate multiple projects in a fast-paced, highly professional environment