Clinical Kit Coordinator

At BioAgilytix, we are passionate about premier science and the impact it has on our world. Our team of highly experienced scientists and professionals deliver tailored services for supporting new medicine breakthroughs with best-in‑class bioanalytical services. We are tirelessly committed to our customers by being solution‑oriented and deadline‑driven, and we are growing. Our culture is fast‑paced, fun, and never boring. Because we work across numerous clients and drug modalities, your career can develop rapidly. You’ll gain experience with a variety of challenges all while you enable life‑changing, life‑saving therapeutics to the patients who need them. The Clinical Kit Coordinator is responsible for supporting the Clinical Kit Department by providing collection kits across Clinical Trials. This position coordinates the assembly and release of clinical kits to meet client expectations and maintain a high level of quality through communication, customer service, and organizational practices. Essential Responsibilities Performs and maintains documentation and compliance standards with adherence to USFDA, OECD, and MHLW Good Laboratory Practices regulations as required Work with team members across the organization: study leads, procurement dept., and lab operations to ensure necessary information is acquired from the protocol to create the lab manuals and kit orders in a timely manner. Track supply inventory and kits, work with Procurement Dept. to re‑order supplies as required. Maintain a working knowledge of different types of collection kits and medical devices, e.g., blood collection tubes, cryo vials, needles. Complete kit work order process, assemble kits, and all required documentation; take part in the quality control process of the kits prior to shipping to clinical sites Provide customs clearance support; upscale issues and advise solutions as necessary. Centralize, streamline, and boost clinical kit processes so that lead times, redundancy, and margin for error are minimized for all clinical trials. Additional Responsibilities Other duties as assigned Minimum Preferred Qualifications - Education/Experience High School diploma Minimum of 1 year of experience in clinical kit production and/or phlebotomy Not less than one (1) year experience in a GxP‑regulated laboratory or clinical environment; clinical kit experience preferred Minimum Preferred Qualifications - Skills Working knowledge of GxP regulations Ability to work in a fast‑paced team environment where multiple concurrent projects must be completed in a timely manner Ability to take direction well and multi‑task Acute attention to detail and excellent organizational skills Excellent oral and written communication skills Proficiency in MS Excel and Word Preferred Credentials Associate degree in molecular biology, chemistry, biochemistry, immunology, biotechnology, or related field Supervisory Responsibility This position has no supervisory responsibilities Supervision Received Frequent supervision and instructions Frequently exercises discretionary authority Working Environment Office environment This position requires the ability to use a computer keyboard, communicate over emails and telephone. Routinely uses standard office equipment such as computers, phones, photocopiers, and filing cabinets Physical Demands Ability to work in an upright and /or stationary position for up to 8 hours per day Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists Frequent mobility needed Occasional crouching or stooping, with frequent bending and twisting of upper body and neck Light to moderate lifting and carrying (or otherwise moving) objects, and laptop computer, with a maximum lift of 30 pounds Ability to access and use a variety of computer software Ability to communicate information and ideas so others will understand, with the ability to listen to and understand information and ideas presented through spoken words and sentences Frequently interacts with others to obtain or relate information to diverse groups Requires multiple periods of intense concentration Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence Ability to perform under stress and multi‑task Regular and consistent attendance Position Type and Expected Hours of Work This is a full‑time position Some flexibility in hours is allowed, but the employee must be available during the "core" work hours as published in the BioAgilytix Employee Handbook Compensation $20 - $22 an hour — In alignment with our compensation philosophy and recruiting governance practices, the salary range for this role represents a good faith estimate of the base compensation for a fully qualified candidate. Individual offers are determined based on a comprehensive evaluation of each candidate’s experience, technical expertise, scope alignment, and internal equity considerations, as well as market data and geographic factors where applicable. As a result, final compensation may fall within or outside of the posted range and will be determined in accordance with applicable state and local pay transparency laws. Benefits and Other Perks Medical Insurance (HDHP with HSA; PPO), Dental Insurance, Vision Insurance, Flexible Spending Account (medical; dependent care), Short Term Disability | Long Term Disability Life Insurance, Paid Time Off (4 weeks per year), Parental Leave, Paid Holidays (9 scheduled; 5 floating), 401(k) with Employer Match, Employee Referral Program Commitment to Equal Opportunity BioAgilytix provides equal employment opportunities to all employees and applicants for employment without regard to race, color, ancestry, national origin, gender, sexual orientation, marital status, religion, age, disability, gender identity, results of genetic testing, service in the military, or any other group protected by federal, state, or local law. #J-18808-Ljbffr BioAgilytix