QUALITY CONTROL ASSOCIATE

K2 Staffing LLC • Maitland, FL

1d • Onsite

About The Position

K2 is seeking a Quality Control Associate to support our clinic out of Orlando, FL. The Quality Control (QC) Associate reviews charts for a specific protocol along with the below additional responsibilities.

Join the K2 Family: Where Compassion and Connection Lead the Way! At K2 Med, people come first and we're seeking warm, wonderful humans who effortlessly click with everyone, from our incredible patients to brilliant physicians and dedicated research staff. We thrive on empathy, a patient-first approach, and absolutely zero big egos (unless it's an ego about being extra kind, then we'll allow it!). We believe a supportive, caring experience is paramount for our patients, and that starts with you.

We celebrate what makes you uniquely you! Your race, color, religion, marital status, age, national origin, or even your favorite snack (though we're partial to good research snacks) don't define your talent or fit here. If you need a little extra support or accommodation due to a disability, no sweat! Just reach out to our friendly team at [email protected] [[email protected]], and we'll ensure you have everything you need to shine.

Requirements

• Strong judgment, planning, and organizational skills
• Ability to manage multiple tasks/projects simultaneously
• Ability to work independently
• In depth knowledge of applicable laws, regulations, and policies
• Strong patient care background; familiar with medical terminology
• Proficient with Microsoft Office
• Learn and support the mission and goals of K2 Medical Research's program
• Ability to communicate clearly/effectively (written and oral)
• Excellent interpersonal and customer services skills
• Bachelor’s Degree required
• Minimum 5 years of clinical research experience with at least 3 years of patientcare experience.
• Applicants that don't meet 100% of the above qualifications but who have a combination of related education, applicable experience, demonstrated capability, and a genuine passion for success in this position may also be considered.

Nice To Haves

• CCRC and/or CCRP preferred.

Responsibilities

• Supports in this role 100% on site out of our Orlando office.
• Duration of this position is for 1 calendar year from start date, or at the conclusion of an FDA Inspection for this study, whichever occurs sooner.
• Systematically perform chart review for this protocol, starting with paper source. The goal is to perform a 100% review of the source documents for this trial.
• Findings will be noted and provided to the study’s Project Director for site staff to address.
• Communicate unusual findings to Quality Management.
• Assist with FDA Inspection preparation and onsite assistance as requested by Quality Management for this protocol.
• Perform ad-hoc projects or other assigned duties on as needed basis.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level