Clinical Research Coordinator II
On-site · Houston, Texas, United States
Houston, Texas, United StatesOn-siteFull TimeMid LevelBachelors DegreeUnknown
Type
Full Time
Level
Mid Level
Education
Bachelors Degree
Company size
Unknown
Job Summary
Clinical Research Coordinator II coordinates multiple concurrent clinical studies, serving as the main contact for sponsors and investigators, ensuring protocol compliance and regulatory documentation, training study team members, managing enrollment and study-related communications, and performing study procedures and data/documentation tasks with strong organizational and communication skills.
Required Qualifications
- BS/BA in Life Science or related discipline or equivalent work experience
- Minimum 3 years of experience coordinating clinical trials
- Strong verbal and written skills
- Bilingual in Spanish and English (location-specific)
- Proficiency with MS Office Suite and regulatory filing systems (e.g., MS Office, SharePoint)
- Ability to travel for site network support, audits and investigator meetings, as required
- Ability to train others on coordinating responsibilities and protocol adherence
- Ability to explain importance of GCP guidelines and their application
- Able to follow clinical research participant safety requirements including ICF process, IRB and adverse event reporting
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