Registered Nurse (RN)

DM Clinical Research

New York (NY)

On-site

USD 50,000 - 70,000

Full time

14 days+

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Job summary

A clinical research organization in New Jersey is seeking a Registered Nurse for an Unblinded Clinical Research Coordinator role. Responsibilities include compounding and dispensing investigational products as part of clinical research trials, ensuring compliance, and maintaining medication records. Candidates should have clinical experience, strong communication skills, and a High School Diploma or equivalent. LPN or CMA credentials are preferred. Bilingual in Spanish is a plus. The position offers a dynamic work environment in a growing sector.

Qualifications

  • Must possess clinical experience.
  • LPN or CMA credentials are required.

Responsibilities

  • Compound and dispense prescribed investigational products.
  • Supervise medication records and ensure compliance with study protocols.
  • Provide consultative support for drug preparation and dosing.

Skills

Excellent communication skills
Customer service skills
Attention to detail
Bilingual (Spanish)
Computer proficiency (Word, Excel, Outlook, Google Docs)

Education

High School Diploma or equivalent
Foreign Medical Graduate

Job description

DM Clinical Research is looking for an Registered Nurse for our Unblinded Clinical Research Coordinator role to join our team in New Jersey. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.

Duties & Responsibilities
  • Compound and dispense prescribed IP.
  • Supervise and maintain records of all medications
  • Ensure compliance with study-specific blinding plans.
  • 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.
  • Manage inventory, ensuring that expired items are removed from the inventory prior to expiration, and purchasing, and delivery processes for the pharmacy.
  • Review protocols and provide input on clinical and pharmacy supply needs.
  • Meet with sponsors, monitors, auditors, and regulatory authorities to review drug accountability and other study-specific information.
  • Temperature reporting.
  • Any other duties/ tasks assigned by the manager, computer proficiency, especially Word, Excel, Outlook, and Google Docs.
Knowledge & Experience
Education
  • High School Diploma or equivalent required
  • Foreign Medical Graduate is a plus
Experience
  • Clinical Experience
Credentials
  • LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant)
Knowledge and Skills
  • Computer proficiency, especially Word, Excel, Outlook, and Google Docs.
  • Excellent communication and customer service skills.
  • Outgoing personality Well-organized with attention to detail.
  • Must be able to multitask.
  • Bilingual (Spanish) preferred but not required
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