Unblinded Clinical Research Coordinator II

Dm Clinical Research Group; Minnesota; On-site; USD 60,000 - 85,000; Full time

Job summary

DM Clinical Research is seeking an Unblinded Clinical Research Coordinator II to join our team. You will dispense Investigational Products and manage IP accountability, ensuring protocol alignment and blinding compliance across trials.

The role requires 2+ years of clinical research experience, relevant credentials preferred, and strong organizational skills to coordinate with sponsors and sites. Fluency in Spanish is a plus.

Qualifications

• Associates degree or 2 years of related coursework required.
• 1+ year of clinical research coordinator experience preferred.
• LPN or CMA credentials preferred; Pharmacy Technician certification preferred.
• Experience with IP dispensing and regulatory documentation is a plus.

Responsibilities

• Dispense Investigational Products (IP) and manage IP accountability records.
• Interpret study protocols to compound and prepare IP for trials.
• Provide training and onboarding support for new team members.
• Maintain site regulatory documents and ensure blinding plans compliance.
• Coordinate with investigators, sponsors, and study managers to meet protocol requirements.

Skills

Communication

Time management

Multitasking

Detail-oriented

Organized

Team collaboration

Bilingual

Education

Associates Degree

2 years coursework

Bachelor's degree

LPN/CMA preferred

Pharmacy Technician Certification

Tools

CRIO

GCP training

Microsoft Word/Excel

Google Workspace

Job description

DM 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 protocolStudy IP managementProvide training and guidance for new team membersAssist in all aspects of company start up activities as requiredSupervise and maintain records of all medicationsEnsure compliance with study-specific blinding plansPerform regular audits on the clinical data to assess percent completeness and accuracyAssist in onboarding training for new membersEnsure external sites’ regulatory documents and required site certifications are up to dateProvide consultative support regarding the preparation and dosing of drugsMaintain documentation of IP accountability: receipt, dispensing, return to sponsor/destructionInterpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trialsUnderstand and apply all applicable site proceduresEnsure receipt and proper storage of IP and bioretention samples, including temperature reportingDevelop operating procedures, guides and best practices for data entry portals and project workflowsInteract 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 managerKNOWLEDGE & EXPERIENCEEducation:Associates Degree required or 2 years of formal educational courseworkBachelor's degree, preferredSecondary or Foreign Medical Graduate, preferredExperience:2+ years of Clinical Research experience, inclusive of in-clinic experience, required1+ year of Clinical Research Coordinator experience, Blinded or Unblinded, required1+ year utilizing CRIO, preferredCredentials:LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant), preferredPharmacy Technician Certification, preferredCompletion of DMCR-required training, including GCP, OSHA and IATAKnowledge and Skills:Computer proficiency, especially Word, Excel, Outlook, and Google Suite products.Excellent communication and customer service skills, both written and verbalExcellent time-management skillsAbility to remain composed under pressure and high-stress situationsOutgoing personalityWell-organized with attention to detail.Must be able to multitask.Bilingual (Spanish) preferred