Our client has an immediate need for several Research Nurses with either Oncology or Neurology. No research experience is needed, this is a perfect opportunity for a nurse trying to get into research.
Description:
Delivers safe care and demonstrates regard for the dignity and respect of all participants.
Maintains adequate skills in clinical competencies including but not limited to physical assessment, phlebotomy and IV insertion.
Practices the principles of Universal Precautions. Understands and abides by HIPAA regulations.
Maintains a clean, prepared clinical space.
May perform set-up and turnover procedures in all clinical areas, per SOP’s, in a timely manner.
Participates in internal and/or external training programs to maintain licensure.
Utilizes positive interpersonal communication skills; communicates effectively with members of the healthcare team, patients, investigators, sponsors of research and administration.
Reviews all elements of the current institutional IRB approved informed consent (IC) document, according to current FDA, state, federal and institutional regulations with study candidates and/or legal representative; ensures, through patient advocacy and informed consent as an ongoing process, that the rights, safety and well-being of trial subjects are the most important considerations and should prevail over the interests of science and society.
Manages multiple clinical trial protocols, coordinates the execution and follow-up of each protocol, seeks and utilizes resources and works independently; performs accurate, legible and timely documentation. Manages records, study medication and test articles in confidential and secure manner.
Promotes Principal Investigator (PI) oversight by advising the PI, sub-investigator(s), Supervisor and/or Clinical Operations Manager of deviations in conduct, patient status, issues relevant to the integrity of the trial and/or the safety of research subjects; abides by hospital and departmental policies and SOPs, as well as all applicable local, state, and federal regulations.
Coordinates the work of support staff, laboratory technicians, and assistants to ensure efficient, timely, and high-quality results and adherence to research protocols.
Serves as liaison between Principal Investigators and the Institutional Review Board (IRB) and the Office of Sponsored Programs (OSP). Prepares and/or reviews all required documentation for clinical research study start up, execution, modification, renewal, and termination and will meet all reasonable deadlines for submission. Maintains timely turnaround of all documents to avoid delays in study initiation and/or progress. Remains current on rapidly changing regulatory requirements and HIPAA regulations and implements these changes as appropriate and in a timely manner.
Collaborates with study sponsors. Assists site monitors during their visits in a professional manner.
Works flexible hours and is available as a resource for questions related to research projects.
Performs other duties as assigned or directed to ensure smooth and efficient operations of the FHRI and Core. Communicates the need for new work and automatically looks for additional duties as workload permits.
Skills:
Clinical trial, Data collection, Oncology, dose calculations, Clinical research, Gcp, Ekg, Registered Nurse
Additional Skills & Qualifications:
Must have 1 year of exp as a RN within oncology * Research exp is a BIG PLUS!
Ability to acclimate and integrate into various clinical settings as needed per protocol
Demonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion and administration of investigational drugs
Working knowledge of Microsoft Office applications, such as, Word, Excel, Access, Outlook, and Internet knowledge and skill
About Actalent:
Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
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