Clinical Research Registered Nurse (RN)

ICON Strategic Solutions; Knoxville (TN); On-site; USD 60,000 - 65,000; Full time

Job summary

A leading company in clinical trials is seeking a Clinical Research Nurse Coordinator in Knoxville, TN. The role involves overseeing trial assignments, ensuring protocol adherence, and training site personnel. Ideal candidates will have RN experience and a degree in a related field. This full-time position offers a competitive salary and benefits.

Benefits

401k

PTO

Qualifications

• 1 year of RN hospital experience required.
• Certification in CPR preferred.

Responsibilities

• Performing clinical requirements of study protocols.
• Monitoring for complications during drug administration.
• Documenting laboratory data and adverse reactions.

Skills

Clinical Research

Venipuncture

Patient Recruitment

Education

4-year degree in Biology

4-year degree in Pharmacology

4-year degree in Clinical Research

Job description

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Clinical Research Registered Nurse (RN) New

Job Title: Clinical Research Nurse Coordinator

Location: Address:

Full time, benefited, 401k, PTO

Hours - M-F 8am-5pm

Pay - 60,000-65,000

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, i.e., 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 intravenous 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 un-blinded 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, within your capacity.

Actively recruiting and effectively promoting our service to suitable patient participants for clinical trials, dedicating set time each week for recruitment efforts.

What You Need:

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

You will receive notifications for jobs within miles of Knoxville, TN.

Be the first to see new jobs near Knoxville, TN!
Enter your email address below to be notified when new jobs are posted.

By creating an alert, you agree to our Terms. You can change your consent settings at any time as outlined in our Terms.