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  3. Unblinded Clinical Research Coordinator I (3777)
Job detail

Unblinded Clinical Research Coordinator I (3777)

DM CLINICAL RESEARCH GROUP

Employer page
#CMA#OSHA#LPN#Pharmacy Technician#Clinical Research#GCP#Clinical Trials#IATA#Regulatory Documents
#CRIO
#Investigational Products
#Sponsor Protocol
OtherOn Site2-5 yrsPosted 3 days agoCloses Jul 27

Location

Albuquerque, New Mexico

Quick overview

Responsible for compounding and dispensing Investigational Products (IP) according to sponsor-approved protocols. Manages IP accountability, maintains regulatory records, and ensures compliance with study-specific blinding plans.

Requirements summary

Requires an Associate's degree and at least 2 years of clinical research experience, including 1 year as a Clinical Research Coordinator. Preferred qualifications include a Bachelor's degree, LPN or CMA certification, or Pharmacy Technician certification.

associate degreebachelor degreeMultitaskingCustomer ServiceTime ManagementOSHAGoogle SuiteMicrosoft ExcelMicrosoft WordRegulatory DocumentationGCPBilingual SpanishInvestigational Product ManagementIATADrug DosingIP AccountabilityCRIOClinical Data Auditing

Job description

Job DetailsJob Location

Albuquerque , NM - Albuquerque, NM 87106DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator I to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.

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

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DM CLINICAL RESEARCH GROUP

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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...

Explore employer profile
IndustryBiotechnology Research
TypePrivately Held
Size501-1,000 employees
HQHouston, TX
Founded2006
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