Sub-I

K2 Staffing LLC•East Providence, RI

11d•Onsite

About The Position

At K2 Medical Research, we are transforming healthcare by delivering tomorrow’s treatments today. As a rapidly growing clinical research organization across Florida, Tennessee, and Rhode Island, we lead multiphasic trials in therapeutic areas ranging from neurodegenerative to cardiometabolic medicine. Our culture is grounded in clinical excellence and a patient-first mission. We are seeking mission-driven individuals ready to play a meaningful role in bringing life-changing treatments to the patients who need them most. K2 is seeking an experienced Clinical Sub Investigator (licensed as a PA, NP or ARNP in the state of RI) to support our clinic out of East Providence, TN. The Sub Investigator promotes Good Clinical Practice in the conduct of clinical investigations by ensuring adherence to protocol requirements, protecting the rights and welfare of study subjects, assuring the integrity of data generated at the site and directing the conduct of the clinical investigation according to federal and state regulations and guidance documents.

Requirements

Licensed Physician Assistant (PA), Nurse Practitioner (NP), or Advanced Registered Nurse Practitioner (ARNP) in the state of RI
2+ years of experience as a PA/NP/ or ARNP.
Experience seeing and providing medical treatment to patients on a daily basis is a must.
Broad knowledge of general medicine and medical terminology
Strong analytical and problem-solving skills
Excellent organizational skills, detail oriented, efficient, and able to multi-task and prioritize effectively.
Excellent interpersonal skills.
BLS and/or ACLS
Strong written and verbal communication skills.

Nice To Haves

licensed to prescribe is a plus
Clinical research experience
experience in neuro or behavioral health preferred

Responsibilities

Provide investigator qualifications and agreements as required for study participation
Maintain current, up-to-date curriculum vitae
Maintain current licensure and continuing education
Assume responsibility for the conduct of the clinical investigation
Maintaining documentation of all aspects of the clinical investigation
Ensure protocol compliance
Ensure initial and ongoing review and oversight by a duly constituted IRB
Provide adequate facilities to conduct the clinical trial
Manage the medical care of study participants (subjects)
Ensure validity of data reported to sponsor
Ensure documentation of study-related procedures, processes, and events
Ensure proper use, storage, and return or disposal of investigational agents
Maintain professional and technical knowledge
Reading, understanding and adhering to organizational Standard Operating Procedures
Assisting in establishing and enforcing departmental standards
Contributes to team effort by: Exploring new opportunities to add value to organization and departmental processes. Helping others to achieve results. Performing other duties as assigned. Learns and maintains Technical and Industry Knowledge by Attending and participating in applicable company-sponsored training.