Demo

Unblinded Clinical Research Coordinator II (3604)

DM CLINICAL RESEARCH GROUP
Indianapolis, IN Full Time
POSTED ON 5/22/2026
AVAILABLE BEFORE 7/22/2026

DM 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

Salary.com Estimation for Unblinded Clinical Research Coordinator II (3604) in Indianapolis, IN
$42,160 to $55,165
If your compensation planning software is too rigid to deploy winning incentive strategies, it’s time to find an adaptable solution. Compensation Planning
Enhance your organization's compensation strategy with salary data sets that HR and team managers can use to pay your staff right. Surveys & Data Sets

What is the career path for a Unblinded Clinical Research Coordinator II (3604)?

Sign up to receive alerts about other jobs on the Unblinded Clinical Research Coordinator II (3604) career path by checking the boxes next to the positions that interest you.
Income Estimation: 
$70,164 - $92,397
Income Estimation: 
$86,269 - $122,182
Income Estimation: 
$42,387 - $56,055
Income Estimation: 
$61,264 - $82,603
Employees: Get a Salary Increase
View Core, Job Family, and Industry Job Skills and Competency Data for more than 15,000 Job Titles Skills Library

Job openings at DM CLINICAL RESEARCH GROUP

  • DM CLINICAL RESEARCH GROUP Irving, TX
  • The Principal Investigator is accountable and responsible for ensuring adherence to protocol requirements, protecting the rights and welfare of subjects, a... more
  • 2 Days Ago

  • DM CLINICAL RESEARCH GROUP Albuquerque, NM
  • A Study Manager is responsible to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Re... more
  • 4 Days Ago

  • DM CLINICAL RESEARCH GROUP Brookline, MA
  • The Clinical Trial Research Manager job is to ensure study enrollment meets or exceeds Sponsors' expectations and company goals are achieved on a timely ba... more
  • 4 Days Ago

  • DM CLINICAL RESEARCH GROUP Phoenix, AZ
  • DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator II to join our team. This individual will be responsible for dispensing ... more
  • 11 Days Ago


Not the job you're looking for? Here are some other Unblinded Clinical Research Coordinator II (3604) jobs in the Indianapolis, IN area that may be a better fit.

  • DM CLINICAL RESEARCH GROUP Indianapolis, IN
  • A CRC III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/... more
  • 11 Days Ago

  • C0001 Franciscan Health Indianapolis Indianapolis, IN
  • Franciscan Health Indianapolis Campus 8111 S Emerson Ave Indianapolis, Indiana 46237 Clinical research helps improve medical treatments and care standards.... more
  • 27 Days Ago

AI Assistant is available now!

Feel free to start your new journey!