Clinical Sub-Investigator

K2 Staffing LLC • Berry Hill, TN

2d

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 TN) to support our clinic out of Nashville, 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

• 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.
• Licensed Physician Assistant (PA), Nurse Practitioner (NP), or Advanced Registered Nurse Practitioner (ARNP) in the state of TN, licensed to prescribe is a plus.
• 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.

Nice To Haves

• Clinical research experience, or experience in neuro or behavioral health preferred.
• Applicants that do not meet 100% of the above qualifications but who have a combination of related education and applicable experience may be considered upon approval.

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.

Benefits

• comprehensive benefits package for full-time employees includes medical, dental, and vision options, supplemental insurance plans, 401(k) with immediate employer match, generous paid time off, and paid holidays
• support a healthy work-life balance through a four-day work week, consisting of 10-hour shifts from Monday through Thursday. Fridays are reserved only for critical business needs or administrative tasks; otherwise, they are your chance to kick-start your weekend.

What This Job Offers

• Job Type: Full-time
• Education Level: No Education Listed
• Number of Employees: 1-10 employees