Research Compliance Project Manager
Company : Catholic Health Initiatives
Location : Phoenix, AZ, 85013
Job Type : Full Time
Salary : 32.38-48.17 HOUR
Date Posted : 1 January 2026
Job Summary and Responsibilities
The Ivy Brain Tumor Center is a non-conventional, non-profit program offering state-of-the-art clinical trials for patients with the most aggressive form of brain cancer. It is home to the largest collection of Phase 0 trials for brain tumors in the world. Our multidisciplinary team of brain tumor specialists and scientists are accelerating drug discovery and precision medicine in neuro-oncology to identify the most promising first-in-class therapies for brain tumor patients.
The Ivy Compliance Project Manager is responsible and accountable for supervising Ivy Center compliance operations across quality management and privacy. This role will drive the implementation of quality and privacy frameworks in alignment with international regulatory requirements, including FDA, ICH, GCP, GDPR, HIPAA, and other applicable data protection laws.
Role Responsibilities:
• Drive implementation of quality management strategy within Clinical Development, with focus on QMS for a Global Phase 3 Registration Study and Early Phase Clinical Trials.
• Develop and maintain a Center of Expertise (CoE) around quality management activities (e.g., deviation, continuous improvement, change control) to ensure ongoing alignment of quality-related goals and strategy.
• Ensure oversight of quality management system by the leadership team including QPPV and Process Excellence & Quality Director.
• Serve as the primary point of contact for global privacy and data protection matters in clinical research.
• Interpret, apply, and monitor compliance with global privacy laws and frameworks (e.g., GDPR, UK GDPR, Swiss FADP, HIPAA, CCPA, APAC privacy laws).
• Oversee implementation of data protection measures, pseudonymization/anonymization standards, and secure data transfer processes across vendors and collaborators.
• Lead Data Protection Impact Assessments (DPIAs) and risk assessments related to clinical trial data.
• Collaborate with Legal/Compliance and external consultants to maintain adherence to global privacy regulations.
• Support regulatory submissions and inspection readiness by ensuring privacy and quality compliance.
• Establish and maintain robust quality systems, including document control, deviations, CAPA, change control, and risk management.
• Oversee the development and implementation of Standard Operating Procedures (SOPs) to ensure consistent adherence to quality and privacy practices.
• Define key quality and privacy compliance metrics and regularly report on the performance of the systems.
• Provide timely updates to senior management on quality and privacy trends, issues, and improvement initiatives.
• Develop and implement training programs for staff on GCP, quality management, and global privacy/data protection requirements.
• Cultivate a culture of quality, compliance, and data stewardship through ongoing education and effective communication.
Job Requirements
Basic Qualifications:
• Extensive experience in quality assurance within the pharmaceutical, biotechnology, or clinical research industry.
• Proven track record of successfully leading quality initiatives and managing regulatory inspections.
• Demonstrated experience with privacy regulations in a clinical research context (e.g., GDPR, HIPAA, CCPA).
• Strong leadership and interpersonal skills, with the ability to influence and collaborate across functions.
• Demonstrated ability to drive a culture of continuous improvement and operational excellence.
• Understanding of Root Cause Analysis and establishing effective corrective and preventative actions.
• Ability to recognize key issues/gaps, quickly develop insight into underlying issues and propose practical strategies.
• Effective communication skills, including the ability to convey complex regulatory and privacy requirements to diverse stakeholders.
• Ability to work effectively/collaboratively cross culturally and cross functionally.
Required Qualifications:
• Bachelor’s degree and/or Master’s degree in healthcare-related or business field.
• Minimum 3 years related experience.
• Prior experience working in the research setting and clinical trial billing.
• Proficient-to-advanced computer skills; proactive, strong organizational skills.
• Excellent verbal and written interpersonal skills.
Preferred Qualifications:
• Supervisory experience or experience in training others, particularly in research.
• Professional certification in research; CCRP, CCRC, or similar.
• Privacy/data protection certification preferred (e.g., CIPP/E, CIPM, CISA, or equivalent).
• Prior experience working in global clinical research settings with exposure to GDPR compliance, vendor oversight, and cross-border data transfers.
Hello humankindness Located conveniently in the heart of Phoenix, Arizona,St. Joseph's Hospital and Medical Center is a 571-bed, not-for-profit hospital that provides a wide range of health, social and support services. Founded in 1895 by the Sisters of Mercy, St. Joseph's was the first hospital in the Phoenix area. More than 125 years later, St. Joseph's remains dedicated to its mission of caring for the poor and underserved. We are extremely proud to be a nationally recognized center for quality quaternary care, medical education and research. St. Joseph's includes the internationally renowned Barrow Neurological Institute, Norton Thoracic Institute, Cancer Center at St. Joseph's, Ivy Brain Tumor Center, and St. Joseph's Level I Trauma Center (which is verified by the American College of Surgeons). The hospital is also a respected center for high-risk obstetrics, neuro-rehabilitation, orthopedics, and other medical services. St. Joseph’s is considered a sought-after destination hospital for treating the most complex cases from throughout the world. Every day, approximately 20 percent of the hospital’s patients have traveled from outside of Arizona and the United States to seek treatment at St. Joseph’s. U.S News & World Report routinely ranks St. Joseph's among the top hospitals in the United States for neurology and neurosurgery. In addition, St. Joseph's boasts the Creighton University School of Medicine at St. Joseph's, and a strategic alliance with Phoenix Children's Hospital. St. Joseph's is consistently named an outstanding place to work and one of Arizona's healthiest employers. Come grow your career with one of Arizona's Most Admired Companies. Look for us on Facebookand follow us on Twitter. For the health of our community ... we are proud to be a tobacco-free campus.
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Frequently asked questions
A Research Compliance Project Manager shapes data privacy by interpreting global laws like GDPR and HIPAA, ensuring clinical trials adhere to these standards. They oversee secure data handling, implement pseudonymization, and lead impact assessments, safeguarding patient information throughout research phases.
Strong candidates often hold degrees in healthcare or business, with 3+ years in pharma or biotech quality assurance. Certifications like CCRP or privacy-focused credentials (CIPP/E, CIPM) enhance prospects, combined with experience navigating regulatory complexities in clinical research.
Phoenix's healthcare sector is rapidly growing, creating competitive demand for compliance expertise. The region's diverse patient base and proximity to international research hubs require managers to adeptly handle multicultural data privacy laws and navigate evolving local regulatory expectations.
Effective leadership empowers cross-functional collaboration, aligning quality and privacy goals across clinical, legal, and vendor teams. Influencing without authority, fostering continuous improvement, and translating complex regulations into actionable plans are key to driving compliance success.
Typically, salaries range between $95,000 and $125,000 annually in Phoenix, reflecting experience, certifications, and the complexity of overseeing global clinical trial compliance. Specialized expertise in privacy laws and quality systems can push compensation toward the higher end.
Catholic Health Initiatives values certifications such as CCRP for clinical research and privacy credentials like CIPP/E or CIPM. These demonstrate mastery over regulatory compliance and data protection, crucial for managing complex clinical trial quality and privacy frameworks.
Daily tasks include overseeing quality management systems, coordinating deviation handling, ensuring SOP compliance, and liaising with leadership on quality metrics. The role demands vigilance to maintain regulatory alignment and drive continuous operational improvements in research settings.
The commitment to serving underserved populations shapes a compliance manager’s focus on ethical research practices and robust data privacy, ensuring clinical trials meet high standards while respecting patient rights, particularly in a diverse community setting like Phoenix.
While both oversee project progress, a Research Compliance Project Manager specializes in enforcing regulatory adherence, privacy safeguards, and quality systems. This role ensures compliance frameworks align with FDA, GDPR, and HIPAA standards beyond routine project coordination.
This position ensures that innovative clinical trials operate within stringent quality and privacy regulations, enabling seamless data integrity and patient protection. Such oversight accelerates neuro-oncology research by maintaining compliance without hindering scientific progress.