Infusion Nurse (PRN)
About The Position
As a member of Adams Clinical’s clinical team, the Infusion Nurse works under the supervision of physician principal investigators and the clinical nurse manager on pharmaceutical-sponsored clinical trials, following FDA regulations and Good Clinical Practice (GCP) guidelines. The role includes IV catheterization and drug infusion, injections, phlebotomy, medical record and laboratory-result review, medication reconciliation, and medical liaison work. Recent bedside experience is ideal; clinical research experience is a plus but is not required. Infusion Nurses work closely with other study-team members and provide mentoring, direction, and guidance to clinical research coordinators. They also support general research activities, including facilitating informed consent, administering screening procedures, entering data, maintaining regulatory binders, and performing other nursing functions as needed. The position is per diem/PRN, with scheduling based on study and clinical needs. Candidates must be available to provide on-site support at least two weekdays per week as needed and be willing to commute to two locations in the Boston, Massachusetts area.
Requirements
- Hold a current, unrestricted license to practice as a Registered Nurse in the Commonwealth of Massachusetts.
- Bachelor’s degree in nursing.
- Availability to provide on-site clinical support at least two weekdays per week as needed.
- Willingness to commute to two locations in the Boston, Massachusetts area.
Nice To Haves
- Recent bedside experience is ideal.
- Clinical research experience is a plus but is not required.
Responsibilities
- Place IVs and initiate and manage IV infusions according to sponsor-provided protocols.
- Assist with difficult phlebotomy and IV placement for phlebotomy.
- Administer subcutaneous and intramuscular injections.
- Review medical records and laboratory results.
- Assist with collection of adverse events, concomitant medications, and medical history.
- Provide medical support on site.
- Work under the supervision of physician principal investigators and the clinical nurse manager on clinical trials in accordance with FDA regulations and GCP guidelines.
- Mentor, direct, and guide clinical research coordinators.
- Facilitate the informed consent process and administer screening procedures.
- Perform data entry and maintain regulatory binders.
- Perform other nursing and research-related functions as required to support clinical trials.
- Commute to two locations in the Boston area and provide on-site support at least two weekdays per week as needed.
- Uphold GCP.
Benefits
- 401(k)
- 401(k) matching
- Opportunities for professional growth and learning.
