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 won’t just manage protocols - you 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 You’ll Do (The Impact You’ll 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 You’ll Love Working With Us

• Meaningful Impact: Help provide life-changing and compassionate care to patients in the Research 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, 1 00% 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 Bachelor’s 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.
• Master’s 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 Driver’s 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.