Unblinded Clinical Research Coordinator II (4015)
On-siteHouston, Texas, United States
Job Summary
Compound and dispense Investigational Products according to Sponsor-approved protocols while managing study IP, maintaining medication records, and ensuring compliance with blinding plans. Perform regular audits on clinical data for completeness and accuracy, interpret clinic schedules to identify preparation timelines, and ensure proper storage and temperature reporting for samples. Provide training and guidance for new team members, assist in startup activities, and develop operating procedures for data entry portals. Maintain documentation of IP accountability and interact with Principal Investigators and study managers to ensure protocol understanding.
Required Qualifications
- Associates Degree
- 2 years of Clinical Research experience
- 1 year of Clinical Research Coordinator experience
- Completion of DMCR-required training, including GCP, OSHA and IATA
Desired Qualifications
- Bachelor's degree
- Secondary or Foreign Medical Graduate
- 1 year utilizing CRIO
- LPN (Licensed Professional Nurse)
- CMA (Certified Medical Assistant)
- Pharmacy Technician Certification
- Computer proficiency, especially Word, Excel, Outlook, and Google Suite products
- Excellent communication and customer service skills, both written and verbal
- Excellent time-management skills
- Ability to remain composed under pressure and high-stress situations
- Outgoing personality
- Well-organized with attention to detail
- Must be able to multitask
- Bilingual (Spanish)
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