Quality Control Associate

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 a Quality Control Associate to support our clinics out of either Maitland or Winter Garden , FL . This position is hybrid with support needed one to two days out of the week at the designated clinics, and remaining days remote. The Quality Control (QC) Associate monitors and performs routine compliance checks on all source data in alignment with protocol requirements and in compliance with ICH-GCP, FDA Regulations, and K2 Medical Research SOPs. Primary Responsibilities: Serving as a point of contact for K2 site(s) regarding quality related questions. Working closely with Quality Management to discuss quality concerns and collaborate resolutions for sites Review of source documents to verify subjects meet Inclusion/Exclusion criteria per protocol requirements to verify eligibility prior to randomization. Review of source documents to confirm adherence to organization policies, procedures and best practices. Create queries for the Project Managers to address missing or incomplete source records or to clarify requirements in the source records. Review of Investigator Site Files to ensure complete, accurate and meeting applicable regulatory requirements. Communicates compliance trends and reports significant quality issues to Quality Management in a timely manner. Assists in ensuring the site(s) are maintaining proper training documents required for GCP and SOP compliance and verifying via eReg. Assists in the tracking and reporting of compliance trends and metrics. Provides training to clinical research staff as needed on quality related procedures and best practices, at the discretion of Quality Management. Perform ad-hoc projects or other assigned duties on as needed basis. Able to commute to assigned location(s) a minimum of once per week, or more, at the discretion of Quality Management. Meet monthly performance goals established for the QC Associate role. Knowledge, Skills, Abilities: 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 Qualifications: Bachelor’s Degree required; CCRC and/or CCRP preferred. Minimum 5 years of clinical research experience with at least 3 years of patient care 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. Your growth and well-being are our priority. Our 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. Most notably, we 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. Join the K2 Family: Where Compassion and Connection Lead the Way! At K2 Medical Research, 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 are an equal opportunity employer. We celebrate what makes you uniquely you and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, marital, or veteran statuses. We value the differences among our team members and are committed to providing reasonable accommodations for qualified individuals with disabilities. If you require a reasonable accommodation to participate in the job application or interview process, please contact [email protected]. We are here to ensure you have the support and tools you need to shine.