Sub-Investigator - Nurse Practitioner/Physician Assistant

Pinnacle Clinical Research•Ridgewood, NJ

30d

About The Position

Come join our team and make a difference as we blaze the way into the future of medical discovery through world-class clinical research. At Pinnacle Clinical Research, we are committed to driving innovation and advancing medical knowledge. Through our rigorous research studies, we strive to unlock breakthroughs that have the potential to transform patient care and improve lives. We pride ourselves on conducting high quality research as a complement to the medical care that our volunteers receive from their routine care center. Together, we will raise awareness about the importance of clinical research and its role in shaping the future of healthcare. Summary: PCR CRCNJ seeks a Clinical Research Advanced Nurse Practitioner/Physician Assistant who will be listed as a Sub Investigator on ongoing study protocols. The Sub Investigator will be a key member of the team and will be responsible for seeing follow up visits, reviewing labs for study subjects, recruiting subjects into protocols, and working with the clinical operations team.

Requirements

Advance degree from a graduate school; and one to two years related experience and/or training; or equivalent combination of education and experience.
Current advanced registered nurse practitioner or physician assistant license.
Valid driver’s License
Written and oral communication skills
Organizational skills
Ability to pay attention to detail
People skills including possessing a positive, friendly, and professional demeanor
Ability to be flexible with changing priorities
Ability to communicate in a diplomatic and professional manner
Strong interpersonal skills
Strong mathematical knowledge
Excellent computer skills knowledge of Microsoft Office, Internet Explorer, Google Chrome, Mozilla Foxfire, and web-based enterprise solutions software.

Nice To Haves

Specialization in geriatrics, internal medicine, or family medicine
Ability/certification to do infusions is a plus
Experience with pharma-sponsored clinical trials strongly preferred
GCP Training certification preferred

Responsibilities

Works with affiliate or collaborating research sites.
Maintains subject and document confidentiality at all times and understands and complies with the appropriate sponsor requirements, regulations including the Food and Drug Administration, good clinical practice, International Conference on Harmonization, Health Insurance Portability and Accountability Act, Institutional Review Boards, and institutional policies and procedures.
Performs study related procedures such as physical examinations, informed consent, subject history, adverse events, test article handling, appointment scheduling, records review, treatment coordination, collecting vital signs, and subject health assessments.
Reviews and holds expert knowledge of study related activities and protocols.
Adheres to study protocols, Food and Drug Administration regulations, and good clinical practices at all times.
Assists in the preparation for study monitor visits.
Performs subject screening and recruitment.
Exercises judgement within the allowable limits defined within clinical trials protocols, standard operating procedures, and under the direction from the principal investigator.
Interacts with internal and external personnel such as physicians, nurses, administration staff, industry sponsor representatives, central laboratory and imaging personnel, and clinical trial patients.
Coordinates multiple projects with competing priorities and deadlines as needed based on clinical trial protocol directives and study volume.