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  3. Unblinded Clinical Research Coordinator II (4015)
DM CLINICAL RESEARCH GROUP logo

Unblinded Clinical Research Coordinator II (4015)

DM CLINICAL RESEARCH GROUP·Houston, Texas

Other·On Site·2-5 yrs·Posted 1 day ago
Practice for this role

About the role

The Unblinded Clinical Research Coordinator will be responsible for compounding and dispensing investigational products while ensuring strict adherence to study protocols and blinding plans. They will also manage site regulatory documents, perform data audits, and provide training and guidance to new team members.

Job DetailsJob Location

CyFair - Houston, TX 77065DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator II to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials. Pharmacy Technicians, LPN's and CMA's are encouraged to apply!

Duties & Responsibilities

Compound and dispense prescribed IP as needed by Sponsor approved protocol Study IP management Provide training and guidance for new team members Assist in all aspects of company start up activities as required Supervise and maintain records of all medications Ensure compliance with study-specific blinding plans Perform regular audits on the clinical data to assess percent completeness and accuracy Assist in onboarding training for new members Ensure external sites’ regulatory documents and required site certifications are up to date Provide consultative support regarding the preparation and dosing of drugs Maintain documentation of IP accountability: receipt, dispensing, return to sponsor/destruction Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials Understand and apply all applicable site procedures Ensure receipt and proper storage of IP and bioretention samples, including temperature reporting Develop operating procedures, guides and best practices for data entry portals and project workflows Interact with Principal Investigator, sponsor, study manager and other study coordinators to ensure all aspects of protocols and study requirements are understood. Any other duties or tasks assigned by the manager KNOWLEDGE & EXPERIENCE Education: Associates Degree required or 2 years of formal educational coursework Bachelor's degree, preferred Secondary or Foreign Medical Graduate, preferred Experience: 2+ years of Clinical Research experience, inclusive of in-clinic experience, required 1+ year of Clinical Research Coordinator experience, Blinded or Unblinded, required 1+ year utilizing CRIO, preferred Credentials: LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant), preferred Pharmacy Technician Certification, preferred Completion of DMCR-required training, including GCP, OSHA and IATA Knowledge and Skills: 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) preferred Qualifications

Requirements

Candidates must have at least 2 years of clinical research experience and an associate degree or equivalent coursework. Preferred qualifications include a bachelor's degree, pharmacy technician certification, or licensure as an LPN or CMA.

  • associate degree
  • bachelor degree
  • Multitasking
  • Communication
  • Documentation
  • Microsoft Office
  • Google Suite
  • Compounding
  • Customer service
  • Dispensing
  • Time management
  • Regulatory compliance
  • Patient safety
  • Clinical research
  • CRIO
  • Data auditing
  • Protocol interpretation
  • Investigational product management

Posting details

Employment type
Other
Work arrangement
On Site
Experience
2-5 yrs
Location
Houston, Texas
Posted
Jul 29, 2026
Closes
Sep 28, 2026
Application
Employer website
DM CLINICAL RESEARCH GROUP logo

Hiring organization

DM CLINICAL RESEARCH GROUP

DM Clinical Research is a network of clinical trial investigator sites with headquarters based out of Houston, Texas. We are the link connecting pharmaceutical and research organizations to caring individuals seeking to power the advancement of medicine. We work with qualified...

IndustryBiotechnology Research
TypePrivately Held
Size501-1,000 employees
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