Job Description

Facility: Valleywise Health Medical Center

Department: Research Administration

Schedule: Regular FT 40 Hours Per Week

Shifts: Days

Are you ready to take the next step in your research leadership career? At Valleywise Health, we are committed to advancing healthcare through groundbreaking clinical research that shapes the future of patient care. We’re hiring a Clinical Research Manager to join our team and play a pivotal role in driving the success of our clinical trials and academic studies.

In this role, you’ll oversee the full lifecycle of clinical studies-from protocol development to final reporting-ensuring projects are delivered on time, with quality, and in full compliance with IRB, GCP, and regulatory standards. You’ll serve as a key problem solver, proactively addressing challenges while leading initiatives to streamline processes, improve outcomes, and deliver meaningful results that directly impact patients’ lives.

This is your opportunity to combine operational expertise, regulatory knowledge, and leadership skills to make a lasting contribution to both science and patient care.
Join us in driving innovation at Valleywise Health!

Annual Salary Range: $93,496.00 - $137,904.00

Qualifications
Education:
  • Requires a Bachelor’s Degree in a clinical research or related technical 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.
  • A Master’s Degree in a related field is preferred and may substitute for two (2) years of required experience.

Experience:
  • Must have a minimum of five (5) years of progressively responsible clinical trial and/or academic research experience in a Pharmaceutical, Biotech or CRO company or Academic Research Institution that includes conducting, managing, monitoring, analyzing or reporting on clinical and academic research.
  • Experience must also include either direct or indirect supervisory-related duties.
 
Certification/Licensure:
  • Requires SoCRA certification as a Certified Clinical Research Professional (CCRP) ; or ACRP/APCR certification as a Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Associate (CCRA), CRC or Certified Principal Investigator (PI).
  • Requires Basic Life Support (BLS) certificate issued by the American Heart Association.
 
Knowledge, Skills, and Abilities:
  • Must have knowledge of the principles, methods, and procedures of basic medical and/or clinical research.
  • Requires Must have excellent communication skills (interpersonal, written, verbal), skill in the use of personal computers and related software applications.
  • Requires Must have the ability to analyze and interpret data and prepare evaluative summary reports and correspondences.
  • Must have excellent organizational and time management skills with strong attention to detail and prioritizing.
  • Requires Must have advanced knowledge of medical research coordination, administration, and fiscal control principles and procedures.
  • Must have skills in organizing resources and establishing priorities.
  • Must have the ability to develop, plan, and implement short- and long-range goals; and provide technical leadership and direction to staff members.
  • Requires Must have knowledge of scientific experimental design and protocol development procedures.
  • Must have sScientific data management skills, using advanced computerized data analysis techniques is preferred.
  • Must be skilled in examining and evaluating operations and developing and/or re-engineering operating strategies, systems, and procedures.
  • Must have ability to supervise and train employees, to include organizing, prioritizing, and scheduling work assignments, and employee development and performance management skills.
  • Requires Must have knowledge of Good Clinical Practice (GPC)GCP guidelines and Occupational Safety and Health Administration (OSHA) standards; human and/or animal research policies, regulations, procedures, and standards, as applied to IRB and compliance operations; and building and leading project teams, ideally in a cross functional capacity.
  • Requires the ability to read, write and speak effectively in English.

Application Instructions

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