NURSE PRACTITIONER (PRN)
Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you!
QPS’ Story:
Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of services, including Early Phase Clinical and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.
Team members enjoy challenging and rewarding work and are encouraged to achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, teamwork and a friendly atmosphere where performance is recognized and rewarded. We provide unique company training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.
If this sounds like your ideal work environment, then we would love to speak with you, so apply for our PRN Nurse Practitioner opportunity today!
Please visit our website (www.qps.com) for more information and to see all current openings.
Summary
The Nurse Practitioner is expected to oversee Phase I, II, III, and IV clinical studies and is responsible for evaluating the safety of the study participants during study conduct.The Job
Executes clinical research trials in strict compliance of study protocol, standards of Good Clinical Practice, Standard operating procedures, QA/QC procedures, OSHA guidelines, Food and Drug Administration (FDA) guidelines and other state and local regulations where applicable.Provide scientific and technical leadership during study conduct.Actively participate in dosing and evaluating study participants for any adverse reactions.Provide technical guidance to others in resolving challenging issues during study conduct.Participate and engage in pre and post study evaluations.Provide technical guidance on study conduct.Meets regularly with the principal investigator and research teams to discuss subject participation and protocol progress. Effectively and professionally communicates with subjects, research teams, IRBs and sponsors. Work with sponsor and internal resources to assist with the plan, design, and coordination of study conduct.Communicate timely and effectively with internal and external clients in regards to technical issues and other study related progress.Review protocols and evaluate from a technical and safety perspective.Review and sign off on all SOP’s.Follow all safety precautions.Requirements
Current state licensureCompletion of master’s degree in designated professionClinical research experience preferred.Strong knowledge of FDA/GCP/ICH guidelines.
QPS is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.