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Clinical Research Registered Nurse (RN)

ICON Strategic Solutions

Winston-Salem (NC)

On-site

USD 80,000 - 100,000

Full time

25 days ago

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Job summary

A leading company is seeking a Clinical Research Nurse Coordinator for a 1-year contract in Winston-Salem, NC. The role involves performing clinical tasks for clinical trials, including patient monitoring and documentation. Candidates should have an RN license or a relevant degree, with a focus on clinical research. This position offers a competitive hourly rate of $40-45 and requires 1 year of RN hospital experience.

Qualifications

  • 1 year of RN hospital experience required.
  • Certification in CPR preferred.
  • Limited travel may be involved.

Responsibilities

  • Completing trial assignments autonomously and accurately.
  • Performing technical and clinical requirements of study protocols.
  • Training site personnel on clinical procedures.

Skills

Clinical Research
Venipuncture
Patient Monitoring
Documentation

Education

RN or 4-year degree in Biology, Pharmacology, Clinical Research, or health-related field

Job description

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Clinical Research Registered Nurse (RN) New

Job Title: Clinical Research Nurse Coordinator, 1 year contract

Location: 1901 S Hawthorne Rd #306, Winston-Salem, NC 27103

Full time, No benefits

Hours: M-F 8am-5pm

Pay: $40-45/hr

We are looking for 1 year of RN hospital experience, no prior research experience needed!

The position is responsible for completing trial assignments in an autonomous, accurate, and timely manner. This position involves staff development and training responsibilities.

Essential Functions: Promoting the mission of PMG to function as an Integrated Site Network providing unparalleled service to our clinical trial partners. Actively striving to meet and exceed action items as discussed quarterly with direct supervisor. Adhering to the study protocol and maintaining proper documentation according to the protocol, regulatory requirements, and internal SOPs. Preparing and administering study medication at the direction of the Investigator. Training site personnel on clinical procedures and CPR/Heartsaver.

Responsibilities:

  • Performing technical and clinical requirements of study protocols, e.g., venipuncture, specimen processing, vital signs, electrocardiograms, IV infusions, IV pump operations, Holter monitoring, pulmonary function testing, allergy testing, urine/serum pregnancy testing, strep throat screening, injections (IM or SQ), or any procedure necessary for the protocol as ordered by the investigator.
  • Attending investigator meetings, site initiation visits, and coordinator meetings to obtain training on drug preparation and administration and general knowledge about a protocol with a focus on clinical procedures.
  • Obtaining knowledge about the study drugs with an emphasis on injection or intravenous infusion medications.
  • Monitoring for possible complications with the administration of study drugs, especially injections or infusions.
  • Maintaining accurate dispensing logs, separate from those of the coordinator, including lot number, drug vs. placebo, and information about the third-party mixer or unblinded preparer of medication.
  • Documenting laboratory data and adverse reactions, and immediately notifying investigators, sponsors, and the Institutional Review Board of any unexpected or serious events.
  • Assisting other staff members as needed, based on the needs and priorities of the research organization.

Actively recruiting and effectively selling our service to suitable patient participants for clinical trials, with set weekly time for recruitment efforts.

What You Need:

RN, or a 4-year degree or equivalent preferably in Biology, Pharmacology, Clinical Research, or a health-related field. Clinical Research Nurse Coordinators should be certified or working towards certification in cardiopulmonary resuscitation. This position may involve limited travel, including flights, to attend investigator meetings.

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