1,000+ matching jobs for “Program Operations Manager”
How results work Exact titles rank first, then title variations and keywords in descriptions. These labels aren't qualification scores. Without keywords, recently added jobs appear first.
Chicago / Adams - IL
Pay posted by employer $72,000–$86,000
The Senior Program Lead, Early Careers partners with Early Careers leadership to translate program priorities into coordinated …
Added Nov 5, 2026
Hanoi, Hanoi, Vietnam
… swift acceleration of digital commerce make these markets some of the most exciting in the world. What a Manager Strategy, Business Planning and Operations does at Visa: The successful candidate will leverage …
Added Oct 27, 2026
Perryville, Maryland
Pay posted by employer $154,000–$231,000
Medline is seeking a hands-on Director of Operations to lead our Perryville Distribution Center. This highly visible role offers the opportunity to strengthen …
Added Nov 3, 2026
India - Hyderabad
… and human genetic data to push beyond what’s known today. ABOUT THE ROLE The EOS & EHS Operational and Program Excellence Associate supports the adoption, execution, data quality, and continuous improvement of …
Added Oct 15, 2026
Boston, Massachusetts, United States
Pay posted by employer $180,000–$270,000
General Summary: The Director, Marketing Operations , Promotional Materials Management will lead Vertex’s centralized promotional materials operations function …
Added Oct 18, 2026
Culver, IN, USA +3 locations 4 postings
Within a division, the Operations Supervisor – Hauling Operations is responsible for supervising the collections activities in one or more …
Added Nov 3, 2026
Perry Hall, Maryland, United States
Pay posted by employer $78,900–$108,450
Within a division, the Operations Supervisor – Landfill is responsible for supervising a team of Lead Operators, Operators and/or General …
Added Nov 3, 2026
Warrington, England, United Kingdom
… resolution. Build strong relationships with Internal Sales teams. Escalate issues promptly to the Sales Operations Team Leader or Manager. Proactively support the business, including working shift patterns as required. …
Added Oct 30, 2026
LNE
Live Nation Entertainment
Los Angeles, California, United States
… this sounds like you then please read on! THE JOB The Wiltern is seeking a highly motivated and proactive Operations /Maintenance professional to join The Wiltern Theatre team. This position will be hands-on experience in an …
Added Oct 16, 2026
Omaha, Nebraska, United States
… outcomes across channels. Use data-driven metrics to identify trends, optimize workflows, and report program performance to senior leadership. Build and mentor a high-performing team, set performance expectations, …
Added Nov 3, 2026
Boston, Massachusetts, United States
Pay posted by employer $242,200–$363,200
General Summary: The Senior Director, Portfolio & Program Management is a global role within the Program and Portfolio Management (PPM) organization. The incumbent …
Added Nov 5, 2026
(USA) San Bruno - 850 Cherry CA San Bruno Home Office
Pay posted by employer $117,000–$234,000 per year
... The Senior Manager , RCM – Billing Strategy & Process Excellence is a senior individual contributor responsible for shaping and …
Added Oct 27, 2026
Minneapolis, Minnesota, United States +1 location
Pay posted by employer $21.35–$29.37 per hour
Join our Alternative Investments Operations team! In this role, you will independently process, reconcile, and balance assigned products while ensuring …
Added Nov 3, 2026
Minneapolis, Minnesota, United States +1 location
Pay posted by employer $44,000–$66,000 per year
… requests in a fast-paced, customer-focused, team environment. Ensure comprehensive and seamless operations for all transaction requests with minimal direction. Work with both internal and external business partners …
Added Nov 3, 2026
USA > KY > Brooks > 420 International
Support front line operations supervisors in determining root causes by teaching/facilitating the use of various root cause methods. …
Added Oct 27, 2026
Budapest, Hungary +3 locations 2 postings
… and functional teams. Act as a strategic partner and senior point of contact for clients, providing program leadership and executive-level stakeholder management. Establish and maintain program governance …
Added Oct 15, 2026
Chaska, Minnesota, United States +1 location
Pay posted by employer $135,000–$145,000 per year
… Learn about the Danaher Business System which makes everything possible. The Technical Project Manager , Global Operations for Beckman Coulter Diagnostics is responsible for the continuous improvement, global …
Added Nov 7, 2026
USA - Mt. Pleasant IA 52641
Operations Management Trainee – Job Description BUILD ON YOUR CAREER WITH A COMPANY THAT HAS A FUTURE At Ryder, our …
Added Nov 3, 2026
Taipei, Taiwan, Taiwan
Full time (company default)
… business value (e.g., accelerating omnichannel coverage and expanding reviewable SKUs) Own end-to-end program schedules, mitigate risks, and drive global teams toward demanding, non-negotiable deadlines Basic …
Added Oct 29, 2026
Newbury, England, United Kingdom
… departmental consumables. May also support the team with processing purchase orders in Enterprise Resource Program (or equivalent), monitoring stock and demand of disposable products (washing and packaging material) for …
Added Oct 27, 2026
Budapest, Hungary +3 more
Same role posted 2 times, once per location
What We're Looking For · employer excerpt Bachelor's degree in Life Sciences, Pharmacy, Regulatory Affairs or a related discipline. Advanced degree preferred. Significant experience within Regulatory Affairs, Regulatory Operations, Regulatory Strategy or related pharmaceutical regulatory functions. Proven experience leading large, complex global programs or portfolios within a CRO, pharmaceutical or biotechnology environment. Strong understanding of global regulatory frameworks, submission management, product lifecycle management and drug development processes.
About this opportunity Original employer description At IQVIA, we help life sciences organizations accelerate the development and commercialization of innovative therapies that improve patient outcomes worldwide.
We are seeking an experienced Associate Program Director, Regulatory Affairs to join our Global Regulatory Affairs team in Eastern Europe. In this strategic client-facing role, you will lead complex global regulatory programs for pharmaceutical, biotechnology and healthcare clients, ensuring the successful delivery of regulatory solutions across the product development lifecycle.
As a senior leader within our Regulatory Affairs organization, you will oversee multiple regulatory workstreams, drive program governance, manage client relationships at senior levels and collaborate with regulatory experts to develop innovative, scalable solutions. You will serve as a trusted partner to clients, balancing operational excellence, financial performance and strategic growth opportunities while helping shape the future of IQVIA's Regulatory Affairs business.
This position offers the opportunity to work across diverse regulatory disciplines, engage with global stakeholders and contribute directly to business expansion through consulting, proposal development and strategic client engagement.
What You'll Do
Lead complex global Regulatory Affairs programs, ensuring successful delivery across multiple projects, workstreams and functional teams. Act as a strategic partner and senior point of contact for clients, providing program leadership and executive-level stakeholder management. Establish and maintain program governance structures, oversight plans, KPIs and delivery frameworks. Drive program planning, financial management, forecasting, resource strategy and operational execution. Oversee cross-functional regulatory teams spanning Regulatory Strategy, Regulatory Operations, Submissions, Labeling, CMC, Safety, Regulatory Intelligence and Lifecycle Management. Identify program risks, dependencies and opportunities, developing proactive mitigation and escalation strategies. Ensure delivery of high-quality regulatory solutions that meet client objectives, business requirements and regulatory expectations. Monitor program performance, profitability, utilization and revenue realization, taking corrective action where needed. Lead governance meetings, steering committees and executive business reviews with clients and senior internal stakeholders. Provide strategic oversight and guidance on regulatory delivery models, resourcing approaches and operational best practices. Partner with Business Development, Consulting and Subject Matter Experts to develop client solutions and expand existing relationships. Lead proposal development, bid defense activities, scope definition, pricing discussions and resource planning for new opportunities. Identify opportunities for account growth and contribute to the expansion of IQVIA's Global Regulatory Affairs offerings. Mentor project managers and other team members, promoting knowledge sharing, capability development and delivery excellence. Drive continuous improvement initiatives and contribute to the evolution of regulatory program management practices across the organization.
What We're Looking For
Bachelor's degree in Life Sciences, Pharmacy, Regulatory Affairs or a related discipline. Advanced degree preferred. Significant experience within Regulatory Affairs, Regulatory Operations, Regulatory Strategy or related pharmaceutical regulatory functions. Proven experience leading large, complex global programs or portfolios within a CRO, pharmaceutical or biotechnology environment. Strong understanding of global regulatory frameworks, submission management, product lifecycle management and drug development processes. Professional fluency in English and French is required, including the ability to lead client meetings, manage complex stakeholder discussions and contribute to business development activities in both languages.Demonstrated success managing complex client engagements and building long-term strategic partnerships. Experience leading cross-functional and geographically dispersed teams in matrix environments. Strong financial acumen with experience managing program budgets, revenue forecasts, profitability and resource planning. Experience overseeing multiple concurrent projects, priorities and stakeholders. Proven contribution to business development activities including proposals, bid defenses, solution design and client presentations. Excellent communication, negotiation and influencing skills, including experience engaging executive-level stakeholders. Strong analytical, problem-solving and decision-making capabilities. PMP, PRINCE2 or equivalent project/program management certification is advantageous. Preferred
Experience leading global or regional Regulatory Affairs programs for large pharmaceutical or biotechnology organizations. Experience managing strategic accounts and long-term client partnerships. Regulatory consulting experience within a CRO or professional services environment. Experience with Veeva Vault RIM, Regulatory Information Management systems and digital regulatory technologies. Experience supporting European regulatory procedures, Clinical Trial Applications, lifecycle management and global Health Authority interactions. Knowledge of emerging regulatory trends, digital transformation and AI-enabled regulatory solutions. Experience participating in organizational growth initiatives, capability development or practice leadership.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
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