Clinical Research Coordinator II

Join Valleywise Health and elevate your clinical research career! As a Clinical Research Coordinator II, you will champion our prospective specimen collection research studies from concept to execution. Working under the guidance of our Program Manager of Academic Research, you wont just manage protocolsyou will actively shape the future of medicine. In this role, you will analyze high-impact clinical data, ensure the highest standards of study compliance, and serve as a vital leader and mentor within our research team. If you are a seasoned researcher looking to drive clinical excellence in a dynamic hospital environment, we want you on our team. What Youll Do (The Impact Youll Make): Drive Discovery: Direct, organize, and launch prospective specimen collection activities that power groundbreaking research. Lead Mentor: Take center stage in developing fellow coordinators, sharing best practices, and fostering a collaborative, growth-oriented team culture. Maintain Excellence: Analyze clinical data with precision, ensuring every study aligns perfectly with protocols and big-picture clinical objectives. Why Youll Love Working With Us: Meaningful Impact:Help provide life-changing and compassionate care to patients in theResearch department. Professional Growth:Valleywise Health is the largest teaching hospital in the valley. Opportunities exist for continuing education, advanced certifications, and exposure to the latest technologies. Supportive, Specialized Team: Join a warm, highly skilled group of physicians, nurses, and healthcare professionals dedicated to excellence in patient care. Competitive Benefits:Robust compensation, 100% matched Pension retirement plan, comprehensive health coverage, paid time off, and more. Annual Salary Range: $51,916.80 - $76,585.60 Qualifications Education: Requires a Bachelors degree preferably in biological sciences or related medical/scientific field; or an equivalent combination of training and progressively responsible experience that will result in the required specialized knowledge and abilities to perform the assigned work. Masters degree is preferred. Experience: Must have a minimum of three (3) years of clinical research experience, preferably in a large healthcare system. Specialized Training: Must have Human Subjects Protection Training or be able to obtain within 14 days of hire. Certification/Licensure: Must possess a current valid Arizona Drivers License. Also requires SoCRA certification as Certified Clinical Research Professional; or ACRP/APCR certification as a CRA, CRC or PI must be obtained within 12 months of employment in position. Knowledge, Skills Abilities: Must have excellent interpersonal and communication skills (oral and written) and be proficient in medical terminology, grammar, spelling and punctuation. Must have strong computer skills in Microsoft Office applications. Requires excellent project management skills. Bilingual a plus. Must have the ability to rotate being on-call and the ability to travel. Requires the ability to read, write and speak effectively in English.