Real
Senior Director, Clinical Quality Assurance
Join to apply for the
Senior Director, Clinical Quality Assurance
role at
Real Base pay range:
$230,000.00/yr - $310,000.00/yr Senior Director, Clinical Quality Assurance - Northern NJ (Hybrid) Shape the Future of Clinical Excellence Our client, a global leader in pharmaceutical innovation, is seeking a results-oriented Senior Director of Clinical Quality Assurance (CQA). Based in Northern NJ with a flexible hybrid arrangement (2-4 times a month), this role offers the chance to elevate global clinical quality standards, drive compliance, and foster continuous improvement in a dynamic and collaborative environment. Core Responsibilities
Audit and Compliance:
Develop and execute global CQA strategies, conduct audits, and manage corrective actions to ensure regulatory compliance. Strategic Leadership:
Create clinical quality roadmaps aligned with business goals, promoting innovation and sustainability. Team Development:
Lead and mentor a high-performing team, fostering collaboration and professional growth. Stakeholder Engagement:
Build strong relationships with internal teams, regulatory bodies, and industry stakeholders. Innovation and Technology:
Leverage advanced analytics and technologies to modernize processes and enhance decision-making. Ideal Candidate Profile
13+ years of experience in Clinical Quality Assurance Proven ability to drive strategic initiatives and improve clinical operations Strong leadership skills with a focus on team development and industry trends Expertise in stakeholder management and regulatory collaboration Passion for leveraging digital tools to enhance operational efficiency Why Join?
This role offers a platform to drive innovation, build impactful systems, and improve patient outcomes globally. With opportunities for growth, collaboration, and access to cutting-edge technology, this is your chance to shape the future of pharmaceutical excellence. If you're a visionary leader in Clinical Quality Assurance, apply today to make a difference in the pharmaceutical industry. Equal Opportunity
EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. In addition to base pay, direct-hire employees may be eligible for client offered benefits such as medical, dental, and vision coverage, and paid leave where required by applicable law. Eligibility may vary based on factors such as location and hire date and is subject to change. To find out more about Real, please visit www.realstaffing.com Job Function
Manufacturing, Other, and Quality Assurance Industries: Pharmaceutical Manufacturing Note: This description reflects the current role and does not include all responsibilities of the position.
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Join to apply for the
Senior Director, Clinical Quality Assurance
role at
Real Base pay range:
$230,000.00/yr - $310,000.00/yr Senior Director, Clinical Quality Assurance - Northern NJ (Hybrid) Shape the Future of Clinical Excellence Our client, a global leader in pharmaceutical innovation, is seeking a results-oriented Senior Director of Clinical Quality Assurance (CQA). Based in Northern NJ with a flexible hybrid arrangement (2-4 times a month), this role offers the chance to elevate global clinical quality standards, drive compliance, and foster continuous improvement in a dynamic and collaborative environment. Core Responsibilities
Audit and Compliance:
Develop and execute global CQA strategies, conduct audits, and manage corrective actions to ensure regulatory compliance. Strategic Leadership:
Create clinical quality roadmaps aligned with business goals, promoting innovation and sustainability. Team Development:
Lead and mentor a high-performing team, fostering collaboration and professional growth. Stakeholder Engagement:
Build strong relationships with internal teams, regulatory bodies, and industry stakeholders. Innovation and Technology:
Leverage advanced analytics and technologies to modernize processes and enhance decision-making. Ideal Candidate Profile
13+ years of experience in Clinical Quality Assurance Proven ability to drive strategic initiatives and improve clinical operations Strong leadership skills with a focus on team development and industry trends Expertise in stakeholder management and regulatory collaboration Passion for leveraging digital tools to enhance operational efficiency Why Join?
This role offers a platform to drive innovation, build impactful systems, and improve patient outcomes globally. With opportunities for growth, collaboration, and access to cutting-edge technology, this is your chance to shape the future of pharmaceutical excellence. If you're a visionary leader in Clinical Quality Assurance, apply today to make a difference in the pharmaceutical industry. Equal Opportunity
EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. In addition to base pay, direct-hire employees may be eligible for client offered benefits such as medical, dental, and vision coverage, and paid leave where required by applicable law. Eligibility may vary based on factors such as location and hire date and is subject to change. To find out more about Real, please visit www.realstaffing.com Job Function
Manufacturing, Other, and Quality Assurance Industries: Pharmaceutical Manufacturing Note: This description reflects the current role and does not include all responsibilities of the position.
#J-18808-Ljbffr